Allulose: The Best Sugar Substitute

Allulose (sometimes D-psicose) is by-far one of the best ways to add sweetness to home-cooked meals in a healthy and low-calorie way. As an epimer of fructose, it has been steadily gaining popularity within the last few years, and not without good reason! Allulose is not only nearly calorie-free, but also decreases blood glucose levels with meals, and seems to have a wide range of potentially beneficial effects.This post is a short summary of why allulose is so appealing over sugar and other sugar substitutes.

70% as sweet; 100% as white and crystalline

Overview of Allulose

Allulose is found naturally in wheat, figs, raisins, maple syrup, and molasses, although in relatively trace amounts. It has around 10% the calories of traditional sucrose and can be manufactured from fructose. It’s around 70% as sweet as sucrose (regular sugar), but has a similar taste and feel, which is a large factor behind why it makes a great substitute (or partial substitute) for baking or dissolving into things. The taste of Allulose has a more natural and relaxing quality than some other sugar-replacement options such as xylitol and erythritol, which are both sugar alcohols, but generally have a ‘cooling effect’ (often likened to the aftertaste of consuming mint, which allulose conveniently lacks).

Allulose is also an actual sugar (not a sugar alcohol or other compound), and has similar browning properties to sucrose via the Maillard reaction. One downside to mention is that it does seem challenging to keep some styles of baked goods crunchy with allulose as the only sugar; while it definitely seems to be one of the best options for sweetening drinks, yogurts, ice creams, cakes, and so on, it may not be the best option for super-crunchy cookies (although can make great softer ones!). This seems to be due to allulose not crystallizing when it cools, its ability to hold more moisture, and that it is more soluble in liquids than sucrose; hence it being a great fit for drinks, sauces, and spongy baked goods.

Allulose was designated as GRAS by the FDA in 2019, so is still relatively new to the market compared to many other sugar substitutes, although has been gaining significant popularity for the short period that it has been available for general usage in foods. I’m sometimes now able to find allulose for sale in a supermarket or included in a sweet good (and it is also now being used in products such as Soylent), although its usage is still a small fraction to that of sugar and corn syrups. It can easily be purchased on Amazon for around $10 per lb (regular sugar is generally closer to $1-2 per lb, so it is quite a bit more expensive if you happen to use very large amounts of sugar).

What Sets Allulose Apart

Why might we want alternative sources of sweetness from sucrose to begin with? Although much has been said about the ways sugars are (in some cases) potentially harmful, it seems reasonable to posit that there are two qualities of a diet with high sugar content (remember, this means any typical western diet!) that are undesirable: firstly, the high caloric content of sugar, which makes over-eating significantly easier and therefore contributes to obesity, and secondly, the effects of sucrose on blood glucose levels and thus insulin resistance, which contributes to diabetes and metabolic syndrome.

As we would hope from an alternative to sucrose, allulose doesn’t cause an increase in blood sugar. The reason for this is that it is not absorbed and digested by the gastrointestinal tract, but rather processed by intestinal bacteria. For the most part this is a good thing, and is what enables allulose to both be low-calorie and to not be converted to glucose in the blood stream. The downside of this is that for some people, especially if consumed in large enough quantities, it can cause mildly discomforting side effects such as flatulence, subpar digestion, and abdominal discomfort. This is much more likely to occur if you, for example, eat an entire batch of allulose cookies by yourself (who would do such a thing..!?), rather than simply use it to sweeten a drink or a snack. While I haven’t experienced anything negative myself, everyone is certainly very different when it comes to food.

But, it gets much better than this! Allulose not only doesn’t increase your blood sugar, but actually decreases it! It does this by inhibiting alpha-glucosidase (along with several other similar enzymes), which is an enzyme that breaks down starches and disaccharides into glucose (i.e. causes carbohydrates to lead to blood glucose spikes). Other well-known inhibitors of alpha-glucosidase include acarbose, a popular and simple diabetic drug which significantly extends lifespan in mice and has the exact same potential side effect profile as large allulose doses (and in my opinion is probably very good for most people to be taking, perhaps extending human lifespan via the same mechanism of action as in mice), and sweet potatoes (source, another source). Thus, adding allulose to meals that contain carbohydrates will result in less of a blood glucose spike than if allulose had been excluded.

Comparison of blood glucose area under curve for small quantities of fructose vs allulose (source: figure 1)

There’s now quite a few studies showing this in humans (and dogs and mice!), with allulose consistently attenuating the postprandial glucose levels both in diabetic and regular adults (effect sizes are often larger in pre-diabetic and diabetic individuals, as is often the case here).

Allulose blood glucose and insulin areas under the curve in comparisons with other sugars (source: figure 2)

But wait, there’s more!

Several studies also appear to show lower plasma triglyceride levels and improved lipid profiles (perhaps via the lowering of hepatic lipogenic enzyme activity, maybe involving SCARB1, but probably many others as well), decreased feeding (perhaps via agonizing glucagon-like peptide-1), enhanced fat oxidation, and a reduction in inflammation related to adipokine and cytokine plasma levels (one paper claims this is partially due to down-regulating gm12250 in mice, but if this applies to humans it may be a side-effect of more upstream metabolic changes more so than specific agonism/antagonism, although as is the case with most foods, things get absurdly complicated very quickly with the amount of pathways involved).

Allulose resulting in reduced feeding in high-fat diet obese and diabetic mice (source: figure 3)

It’s worth noting that several of the above studies (particularly ones that attempt to hone in on specific mechanisms of action) are in mice, and in fact, we could go much further if we want to look at mice; it’s trivial to find many more potentially favorable results such as “Not only metformin, but also D-allulose, alleviates metabolic disturbance and cognitive decline in prediabetic rats” or “D-allulose provides cardioprotective effect by attenuating cardiac mitochondrial dysfunction in obesity-induced insulin-resistant rats“. Although there is less (and sometimes conflicting) evidence for e.g. improved lipid profiles in humans, there is certainly more than sufficient evidence of allulose’s effect on reducing blood glucose levels and overall calories consumed, from which we would naturally expect many other beneficial effects to follow. Searching for allulose on pubmed results in a wonderful selection of studies showing very consistent outcomes in this area, and it thus seems plausible that, at the very least, we would see significant reductions in diabetes and obesity if allulose were to be more widely adopted in consumer food products.

Conclusion

In general it seems like replacing sugar with allulose will result in fewer calories consumed, a lower risk of obesity, lower blood glucose (average and area under the curve, sometimes peak) levels and thus improved insulin resistance and a lower risk of diabetes and metabolic syndrome, and potentially some other beneficial effects (which may or may not apply in humans, but if allulose improves your diet and lowers your food intake, I would not be surprised to see improved lipid profiles and a reduction in inflammation, even if entirely for indirect reasons, e.g. cooking at home with allulose instead of purchasing processed foods from the store. It’s also worth noting that while some of these benefits are a direct result of allulose consumption, many are also partially from a reduced intake of sugar and calories – similar to how cutting down on your sugar intake would offer many benefits).

It’s quite possible that if a notable fraction of other sugars in our diet were to be replaced with allulose, the amount we would gain both in QALYs and dollars saved via the resulting reduced healthcare burden would be extremely favorable. Allulose is still relatively new to the market, and as it is also much more expensive than sugar or corn syrups, its future market penetration may be relatively limited by consumer preferences. Regardless of its presence in our broader food ecosystem, you can start experimenting with it yourself today! (Amazon search results page link, in case this saves you 10 seconds)

I usually use allulose to sweeten drinks, greek yogurt, and sometimes add it to sauces or baked goods in small quantities. I’m also pretty interested in glycine and think it may be something that most of us should be having a lot more of as well (some notes on this in the glycine section on my supplements page), but consider it outside the scope of this article for now. Lastly, if the idea of significantly reducing the glycemic index of your meals is appealing, I strongly suggest looking into acarbose – it is a much stronger inhibitor of alpha-glucosidase, well-tolerated, and also relatively cheap.

If you enjoyed this article you might also enjoy my supplements page which discusses many other ingredients and drugs that I find interesting with respect to longevity. Feel free to reach out with any comments or corrections via any communication method on my about page, thanks for reading!

The Bouba/Kiki Effect And Sound Symbolism In CLIP

The bouba/kiki effect is the phenomenon where humans show a preference for certain mappings between shapes and their corresponding labels/sounds.

One of the above objects shall be called a bouba, and the other a kiki

The above image of 2 theoretical objects is shown to a participant who is then asked which one is called a ‘bouba’ and which is called a ‘kiki’. The results generally show a strong preference (often as high as 90%) for the sharply-pointed object on the left to be called a kiki, with the more rounded object on the right to be called a bouba. This effect is relatively universal (in languages that commonly use the phonemes in question), having been noted across many languages, cultures, countries, and age groups (including infants that have not yet learned language very well!), although is diminished in autistic individuals and seemingly absent in those who are congenitally blind.

What makes this effect particularly interesting is less so this specific example, but that it appears to be a general phenomenon referred to as sound symbolism: the idea that phonemes (the sounds that make up words) are sometimes inherently meaningful rather than having been arbitrarily selected. Although we can map the above two shapes to their ‘proper’ labels consistently, we can go much further than just that if desired.

Which is a takete, and which is a maluma? Only you can decide.

We could, of course, re-draw the shapes a bit differently as well as re-name them: the above image is a picture of a ‘maluma’ and a ‘takete’. If you conformed to the expectations in the first image of this section, it’s likely that you feel the maluma is the left shape in this image as well.

We can ask questions about these shapes that go far beyond their names too; which of these shapes is more likely to be calm, relaxing, positive, or explanatory? I would certainly think the bouba and maluma are all four of those, whereas the kiki and takete seem more sharp, quick, negative, or perhaps even violent. If I was told that the above two shapes were both edible, I can easily imagine the left shape tasting like sweet and fluffy bread or candy, while the right may taste much more acidic or spicy and possibly have a denser and rougher texture.

Sound symbolism

The idea that large sections of our languages have subtle mappings of phonemes to meaning has been explored extensively over time, from Plato, Locke, Leibniz, and modern academics, with different figures suggesting their theorized causes and generalizations.

Some of my favorite examples of sound symbolism are those found in Japanese mimetic words: the word jirojiro means to stare intently, kirakira to shine with a sparkle, dokidoki to be heart-poundingly nervous, fuwafuwa to be soft and fluffy, and subesube to be smooth like soft skin. These are some of my favorite words across any language due to how naturally they seem to match their definitions and how fun they are to use (more examples because I can’t resist: gorogoro may be thundering or represent a large object that begins to roll, potapota may be used for dripping water, and kurukuru may be used for something spinning, coiling, or constantly changing. There are over 1,000 words tagged as being mimetic to some extent on JapanDict!).

For fun I asked some of my friends with no prior knowledge of Japanese some questions about the above words, instructing them to pair them to their most-likely definitions, and their guesses were better than one would expect by random chance (although my sample size was certainly lacking for proper scientific rigor). The phonestheme page on Wikipedia tries to give us some English examples as well, such as noting that the English “gl-” occurs in a large number of words relating to light or vision, like “glitter”, “glisten”, “glow”, “gleam”, “glare”, “glint”, “glimmer”, “gloss”. It may also be worth thinking about why many of the rudest and most offensive words in English sound so sharp, often having very hard consonants in them, or why some categories of thinking/filler words (‘hmm’… ‘uhhh…’) sound so similar across different languages. There are some publications on styles of words that are found to be the most aesthetically elegant, including phrases such as ‘cellar door’, noted for sounding beautiful, but not having a beautiful meaning to go along with it.

Sound Symbolism in Machine Learning with CLIP

I would guess that many of the above aspects of sound symbolism are likely to be evident in the behavior some modern ML models as well. The reason for this is that many recent SOTA models often heavily utilize transformers, and when operating on text, use byte-pair encoding (original paper). The use of BPE allows the model to operate on textual input smaller than the size of a single word (CLIP has a BPE vocab size of 41,192), and thus build mappings of inputs and outputs between various subword units. Although these don’t correspond directly to phonemes (and of course, the model is given textual input rather than audio), it’s still likely that many interesting associations can be found here with a little exploration.

To try this out, we can use models such as CLIP+VQGAN or the more recent CLIP-guided diffusion, prompting them to generate an image of a ‘bouba’ or a ‘kiki’. One potential issue with this is that these words could have been directly learned in the training set, so we will also try some variants including making up our own. Below are the first four images of each object that resulted.

four images of “an image of a bouba | trending on artstation | unreal engine”
four images of “an image of a kiki | trending on artstation | unreal engine”

The above eight images were created with the prompt “an image of a bouba | trending on artstation | unreal engine”, and the equivalent prompt for a kiki. This method of prompting has become popular with CLIP-based image generation models, as you can add elements to your prompt such as “unreal engine” or “by Pablo Picasso” (and many, many others!) to steer the image style to a high-quality sample of your liking.

As we anticipated, the bouba-like images that we generated generally look very curved and elliptical, just like the phonemes that make up the word sound. I have to admit that the kiki images appear slightly less, well, kiki, than I had hoped, but nonetheless still look cool and seem to loosely resemble the word. A bit disappointed with this latter result, I decided to try the prompt with ‘the shape of a kikitakekikitakek’ instead, inserting a comically large amount of sharp phonemes all into a single made-up word, and the result couldn’t have been better:

the shape of a kikitakekikitakeki | trending on artstation | unreal engine

Having inserted all of the sharpest-sounding phonemes I could into a single made-up word and getting an image back that looks so amazingly sharp that it could slice me in half was probably the best output I could have hoped for (perhaps I got a lucky seed, but I just used 0 in this case). We can similarly change the prompt to add “The shape of” for our previous words, resulting in the shape of a bouba, maluma, kiki, and takete:

the shape of a bouba (top left), maluma (top right), kiki (bottom left), and takete (bottom right)

It’s cool to see that the phoneme-like associations within recent large models such as CLIP seem to align with our expectations, and it’s an interesting case study that helps us imagine all of the detail that is embedded within our own languages and reality – there’s a lot more to a word than just a single data point. There’s *a lot* of potential for additional exploration in this area and I’m definitely going to be having a lot of fun going through some similar categories of prompts over the next few days, hopefully finding something interesting enough to post again. If you find this topic interesting, some words you may want to search for along with their corresponding Wikipedia pages include: sound symbolism, phonestheme, phonaesthetics, synesthesia, ideathesia, and ideophone, although I’m not currently aware of other work that explores these with respect to machine learning/AI yet.

Thanks for reading! I appreciate feedback via any medium including email/Twitter, for more information and contact see my about page

Does 17α-estradiol/estrogen extend male human lifespan?

17α-estradiol is a relatively (or completely) non-feminizing form of estradiol (E2), or estrogen. It is a naturally occurring enantiomer of 17β-estradiol (the much more common form of estradiol, usually just referred to as ‘estradiol’) which is found in both male and female humans. This post a a brief essay that discusses the prospect of it extending lifespan in humans. There are two primary types of estrogen receptors, ERα and Erβ, and as you may expect, 17α-estradiol appears to show a stronger binding affinity for ERα. It has a very low binding affinity in locations that generally induce feminization (which appear to be sometimes be both ERα and ERβ), so it’s also possible to take as a male without significantly altering one’s appearance towards the opposite gender. Although we can definitively point to a plethora of effects of regular estrogen, it is difficult to tell what the true purpose of 17α-estradiol is in humans, with Stout et al. (2016) stating “the physiological functions of endogenous 17α-E2 are unclear”. There is evidence it has neuroprotective properties, can help treat Parkinson’s disease, cerebrovascular disease, and much more. This likely involves ER-X, which in turn activates MAPK/ERK and many, many other things down the line (as usual..), but it’s difficult to know for certain. Although these reasons were among the reasons that researchers took into account when deciding to dedicate funding to testing 17α-estradiol in mice for longevity effects, subsequent papers have found more exciting mechanisms of action which are elaborated upon below. For some interesting further reading on this topic that goes into more detail exploring possible mechanisms of action here I’d also suggest reading the following papers: Castration delays epigenetic aging and feminizes DNA methylation at androgen-regulated loci, Hypermethylation of estrogen receptor-alpha gene in atheromatosis patients and its correlation with homocysteine.

17α-estradiol has been found to consistently and significantly extend the median lifespan of male mice, including by the NIH’s Intervention Testing Program, the closest thing we have to a gold standard of longevity RCT experimentation in mice, where three studies are rigorously performed at three separate locations, allowing the results to be instantly compared and reproduced by the two other parties and locations upon completion. Strong et al. (2016) find that 17α-estradiol extends median lifespan of male mice by an average of 19% (26%, 23%, and 9% from the three independent testing sites), and increased the maximum age by an average of 12% (21%, 8%, and 8% from the three testing sites, using the 90th percentile). Harrison et al. (2014) similarly find that median male lifespan was increased by 12%, but did not find an increase in maximum lifespan, and these results have been replicated even more in recent years.

These are some impressive results for such a common and simple endogenous substance! One of the first things we notice is that this effect only applies to males, with female lifespan (both median and maximum) being unaffected. As the substance in question is an estrogen, we can assume that this is either due to female mice already having this benefit, as they already have a sufficient level of it, or that something more complex is at play, and there is a different downstream pathway that is only being activated in males for some reason (more on this later). I had initially assumed the former hypothesis was at least a partial explanation, having known that females consistently live longer than males when it comes to humans, and that this was obviously biological in nature. However, it’s much more complicated in mice as females do not always outlive males, and in fact many times the opposite is true. One meta-analysis (good overview, original book source) finds 65 studies where males lived longer and 51 where females lived longer, with this often depending on the strain of mice used, which varies greatly depending on the type of reseasrch and time period. Regardless, it’s clear there is much more at play in this scenario, and perhaps something special about 17α-estradiol in particular.

Although the ITP studies initially included 17α-estradiol due to the reasons mentioned in the first paragraph, later research such as Stout et al. (2016) has now found that 17α-estradiol not only increased AMPK levels (as some other notable longevity substances such as Metformin also do), but also reduced mTOR activity (complex 1!) in visceral adipose tissue, which is rather reminiscent of Rapamycin, which has extended the lifespan of every organism we have performed an RCT with thus far (and likely can in humans too, if you ask me). In a way, this is significantly more exciting, because it gives us a much more plausible way to explain the lifespan extension effects we are noticing. However, it is also partially a disappointment: if these effects are the real reasons why 17α-estradiol extends male mice lifespan, then this substance may offer us nothing that we do not already have via rapamycin and metformin, among others. The paper also noted that fasting glucose, insulin, and glycosylated hemoglobin were reduced along with inflammatory markers improving. These are similar to the types of positive side effects we would expect from a longevity agent, and the study also notes that no feminization nor cardiac dysfunction occurred.

How do these effects (such as AMPK and mTOR modulation) occur? I don’t know, and apparently neither does anyone else. As is often the unfortunate case in biology, the paper has this to say: “The signaling mechanism(s) by which 17α-E2 elicits downstream effects remains elusive despite having been investigated for several decades”. Perhaps just a few more decades to go and this section will be updated with more information, then. Mann et al (2020) find that male mice without ERα do not benefit from 17α-estradiol, which helps us narrow down the first step by excluding Erβ, ER-X and other less-predictable initial mechanisms. Interestingly, they also note that “both 17α-estradiol and 17β-estradiol elicit similar genomic binding and transcriptional activation of ERα”, which would leave us with the question of why we are focusing on 17α-estradiol specifically, if 17β-estradiol (which is much more common) suffices as well. Importantly, they also seem to think changes in the liver might be involved. Garratt et al. (2018) add that distinct sex-specific changes in the metabolomic profile of the liver and plasma were found, and also notes that the longevity benefit for males disappears post-castration. They first supplement males and females, showing many differences related to metabolism including with amino acids. Then they use castrated males and notice that their profiles are the same as the control group, and thus conclude that they are no longer being positively affected by 17α-estradiol. I am unsure if we should be focusing on the AMKP/mTOR effects (which are very relevant to longevity) or on the liver/metabolic effects (which are also very relevant), or if these are in fact just two different temporal points on the same biological pathway which we don’t yet fully understand, but this helps us connect at least a few more dots.

All of the above sounds exciting, but it’s also all in mice. Sometimes this is useful, as mice are actually quite similar to humans (more so than many may expect), but a lot of it is also less useful or outright misleading. I cannot find a way to take only 17α-estradiol in a safe way as a human, however there is a topical cream of it (alfatradiol) which is used to treat pattern hair loss.

Luckily, one thing that the ITP study found was that 17α-estradiol was among one of the substances that seems to perform well with respect to longevity (if not fully) when given later in life (this has replicated afterwards as well), contrary to some others which have the best effect when started in youth and continued until death. In theory I wouldn’t mind waiting a decade or two until we have a better idea of what is going on here, after which point I would hope we have more fruitful and actionable results (especially in humans); although at the same time there’s likely many reasonable and safe ways we can go about achieving this (hopeful) effect in human males (assigned at birth) already, either via a type of estrogen or an estrogenic drug such as a SERM.

It is worth reminding ourselves that 17α-estradiol is already present in humans, and in both sexes, with women generally having significantly higher levels, as one expects of estrogen. Similarly, regular estrogen binds to both estrogen receptors, including our target, which we now know to be the alpha receptor. Given this, is it possible that just taking regular estradiol (for example, estradiol valerate, which for most purposes ends up biologically equivalent to endogenous estradiol and thus also binds to both primary estrogen receptors) to increase the levels of estrogen is a potential longevity intervention?

This is a difficult question to answer with the data currently available, although there are millions of persons assigned male at birth that are already on various forms of estradiol for various reasons, one of them being to assist in gender transition from male to female. As the lifespan benefit only applied to male (assigned at birth) mice, there would be benefits to analyzing these cohorts for more information, especially if we were able to have DNA methylation clocks used on these groups alongside a control (although this would not be a true RCT, as which persons decide to undergo feminizing HRT would not be random, I suspect we could still get the information we’d want with a good sample size).

There are other potential avenues of statistical analysis that could be attempted here, although they prove to be difficult for various reasons. Most male to female transgender individuals decide to transition earlier in their life, and this was also a particularly uncommon choice to make many decades ago in comparison to the present, so we have very few deaths due to age-related causes that we would be able to analyze to attain a proper hazard ratio. Even if we waited a long time for this (or had this data already), it would be terribly confounded due to the lack of randomization and many potential selection effects. Even so, one of the following must be true:

  • 17α-estradiol does not extend male (assigned at birth) human lifespan
  • 17α-estradiol does extend male (assigned at birth) human lifespan, however this does not apply to most/any transgender (m->f) individuals. This could be due to insufficient dosage, insufficient affinity for the alpha receptor, the inclusion of 17β-estradiol, the common addition of other substances such as anti-androgens, or another unknown factors/confounders
  • 17α-estradiol does extend male (assigned at birth) human lifespan, and this effect therefore does apply to most transgender (m->f) individuals, however we have either failed to notice it completely, or other effects/confounding variables ablate this, for example an increased risk of blood clots from estrogen supplementation (which depends greatly on the route of administration as well as type of estrogen used) or various potential side-effects from anti-androgen usage

Option one is certainly a possibility, as it always is in longevity when all of our studies are only in mice. We could differ too much from mice for the mechanism of action to apply to us (perhaps if it is related to metabolism or some newer subset of liver functionality), or if the mechanism of action is indeed the AMPK/mTOR pathways, perhaps 17α-estradiol does not modulate these in humans as it does in mice. This could have implications for other potential longevity agents such as metformin and rapamycin in humans as well, which also heavily involve these pathways, which could cause these agents to interplay synergistically or perhaps cancel one another out, as there may be no further benefit that can be gained after one of these agents is already taken at the optimal dosage. It is worth noting that many aspects related to AMPK/mTOR and DNA methylation are heavily evolutionary conserved as well (mTOR quite strongly, which is another reason why rapamycin likely extends human lifespan). We also already know that human females have longer lifespans than males for biological reasons, and that there are quite a few reports that the lifespan of castrated males is significantly increased. If 17α-estradiol (or estradiol valerate perhaps) does not extend human male lifespan, I would have to believe there is some other similar route that likely does, and we just have to find the best way to go about pursuing it.

Option two is, in my opinion, moderately plausible. It could the case that when we do have groups that supplement estradiol, the dosage taken is nowhere near sufficient for a noticeable longevity improvement, and that if we would simply increase it by some factor, longevity benefits would become apparent. There does seem to be a dose-dependent relationship for the longevity benefits in mice, and it may be possible that estrogen receptor alpha simply isn’t being agonized nearly enough. This may depend on the type of estrogen and route of administration used, as well as other drugs that may be taken (for example, most male to female transgender individuals take an anti-androgen as well as an estrogen, and this could potentially ablate benefits). My personal conjecture would be that estrogen monotherapy via injections would have the best probability of a longevity benefit for those assigned male at birth, although modulating or combining this with SERMs may also be of interest, although much more experimental and difficult to get right (I may add more to this later as this is a pretty interesting avenue to me for multiple reasons).

As for option three, it may seem difficult at first glance to think that millions of male to female transgender individuals are all currently supplementing a substance that may increase their lifespan by 5-20%, but yet none of us (or them) have noticed this yet. However, there are no preventative reasons for why this couldn’t be the case, nor statistical evidence against this possibility. It could even be that suppressing testosterone and activating estrogen receptor alpha are additive in nature, and we end up with a particularly impressive lifespan extension effect from conventional feminizing HRT.

Although I obviously cannot be sure of any specifics, I do think there is likely some hormonal intervention that should significantly increase male (assigned at birth) human lifespan, but that we just may need another decade or two to get the optimal intervention figured out properly. It would be great to have substances like 17α-estradiol in human trials already, as the potential ROI for successful longevity interventions is massive both in terms of billions of additional QALYs and trillions of dollars saved in healthcare expenditure.

In conclusion, 17α-estradiol might notably extend human lifespan for those assigned male at birth. There are many potential mechanisms of action that could cause this, with the most interesting one perhaps being activation of the mTOR and AMPK pathways, resulting in more ‘feminine’ DNA methylation. This longevity benefit, if it exists, may apply to many male to female transgender individuals, or could also be weaker or stronger for various reasons, such as due to the common usage of anti-androgens. If this longevity benefit does not apply to these groups, there may be alternative hormonal interventions that work instead, such as supplementing 17α-estradiol directly, using a SERM with a strong binding affinity in the right areas, or other modifications to the HPG axis that reduce some potential negative longevity effects of testosterone.

Disclaimer: I’m a random person on the Internet and none of this is medical advice. I’d like to rewrite and expand on the potential mechanisms of actions in this post and talk a bit more about what I do myself in this area some time too. Feel free to mention any corrections or comments to me (see: About page).

Cynical Answers To NFT FAQs

Q: What is an NFT?

A: NFTs are a novel method for some people to make boatloads of money off of others, and in doing so create an entire new ecosystem that primarily uses misinformation to justify its own existence in order to perpetuate profiteering from those at the top.

As one would expect, many previous methods with this MO have existed, including within the cryptocurrency ecosystem, such as ICOs. However, most ICOs ended up being illegal as they not only involved selling unregistered securities to non-accredited investors, but also involved a lot of fraud and deception. NFTs solve this debacle by having a significantly lower legal risk, as they’re unlikely to be considered securities (since I wrote this, many people have come up with wonderful ideas on how to turn them into securities, so this can be considered false for many projects. Regardless of this, there’s enough other laws about fraud being broken that it is often irrelevant.)

Technically, an NFT is an entry (digital file) on a blockchain (large sequence of blocks made up of data and transactions) that is unique, and thus not fungible (interchangeable) with any other token or asset.

Q: How does an NFT put art on the blockchain?

A: It doesn’t. The reason for this is simple: the blockchain is too inefficient to store large amounts of data on; storing as much as a 4MB image on the Ethereum blockchain would currently cost around $72,000, as it needs to be stored on every copy of the blockchain in existence (The math for this is (10^9 / 10*18) * 1000^2*4 * 68 * 150 * 1800, where the constants are the following: wei per gwei, wei per eth, bytes in 4MB, gas per byte, gwei per gas, usd per eth).

Q: If an NFT is not on the blockchain, then where is it?

On a web server somewhere, just like everything else on the Internet. Specifically, the blockchain may have a link to media content, which in the best case would be an ipfs link (which is still sitting on one or multiple computers somewhere, and generally accessed only through centralized gateways), and in the worst case is an http(s) link. Neither of these are guaranteed to remain in existence forever, but at least ipfs (among some other decentralized solutions which are still relatively newer) can be partially decentralized, replicated more easily, and verified more easily. As the blockchain is public, all files are generally public as well. This not only means that the content pointed to by the NFT may not stay up, but also that it could be replaced with anything else, as recently pointed out by Moxie.

Q: What about other NFT information like traits or NFTs listed for sale on websites? That’s the blockchain, right?

Nope. Again, due to the blockchain being prohibitively expensive to store information on, even NFT traits (identifying characteristics/labels for the given token) are generally not stored on the blockchain, but are instead provided via a JSON api, just like the rest of the Internet uses.

Although NFTs are intended to be minted on the blockchain in order to exist, the cost of this started to get too high as fees increased, so now popular websites that users use to create NFTs have a ‘gasless’ minting method, where no blockchain transaction occurs until someone purchases the asset on the website, thus the blockchain is yet again bypassed and a centralized entity is used instead. If you analyze the technical makeup of many popular cryptocurrency projects, this is an extremely common theme; most cryptocurrency blockchains are very expensive, redundant, inefficient, and slow; so centralized systems are used in their place anywhere that users are not directly paying attention to.

In fact, it’s often much worse than this! As pointed out by Moxie, centralized companies like Opensea can remove NFTs from their platform at their own discretion, and ‘decentralized’ extensions such as metamask just query the Opensea API! Working with blockchains is very expensive and difficult and tedious (for a good reason – decentralization is hard and is often worth this effort!), so this is a very common pattern (we are certainly glad actors like Etherscan seem to be impartial, because almost all chain information comes from companies like this rather than from anyone reading the blockchain data themselves!)

Q: If transactions on the blockchain are so expensive, how are users using Ethereum to make cheap and instant transactions?

A: They aren’t, at least not right now. Currently the cost to transfer an Ethereum ERC20 token is $22 and the cost to trade a token with Uniswap is $65 (this seems to have only increased since writing this and constantly changes, so this section will often be out of date). A regular transaction can still be performed for around $6, although this can of course increase arbitrarily according to the market. This price may decrease at some point, but you also never know when the market will increase it drastically, potentially even making ether you own worthless (for example, if the fee to send eth is $6 and you only have $5 of eth in your address, you are out of luck). It is worth knowing there are other solutions (sometimes called L2 / ‘Layer 2’ systems) that are working to improve this on many major blockchains such as Polygon on Ethereum.

Q: How do I receive ownership and the rights to the art I purchase as an NFT?

A: You don’t. As far as ownership goes, there is nothing but a digital signature by an Ethereum address you have the private key to, which is placed on a contract that has a link inside of it of something you happen to like. Anyone can see the link and view the file. Additionally, there is nothing legally binding about this transaction, and there is no guarantee you will have the IP rights to whatever it is you spent your money on. Many popular NFT projects specifically have legal disclaimers telling you that not only do you not own the IP, but they (the creator) does, and you are unable to modify it without their permission.

Q: How can I ensure the original artist is the person selling the NFT?

A: You can’t. Anyone can create an NFT that has any link to any file in it, and there is nothing preventing this from being published on the blockchain by anyone.

As you would expect, there are many instances of users selling art that they did not create. In addition to art being stolen and sold by someone unrelated, resources such as machine learning models and art tools have been used to create valuable NFTs, with the original programmers not only left uncompensated, but un-credited entirely. But at least some random person got $10,000 for taking credit.

Q: Why has the popularity of NFTs been increasing so much?

A: Because people are making easy money with them. Similar to cryptocurrencies, every person that owns them has a vested interest in hyping them up to others in order to profit. The ecosystem as a whole uses many techniques in order to increase its own virality, including stories about how Everyone Is Getting Super Rich Super Quickly Doing Basically Nothing Except For You, significant hype both from excited individuals and from extensive paid shilling campaigns from those that are set to profit from them, and new technical jargon like “Decentralized Ethereum non-fundigle tokens with sidechain and parachain integration using ERC721+ERC1151”.

Q: How can I verify that an NFT purchase was legitimate?

A: You cannot. Although the transaction is on the blockchain and you can verify that it occurred, you do not know who the addresses involved in the transaction belong to. This enables one to create NFTs and then buy them from themselves using different addresses that they own in order to give the appearance that they are valuable and in high demand, effectively painting the tape with the hope that someone else (who, unfortunately, doesn’t understand this is occurring), will then will pay a large amount for something no one else actually wanted. For example, the recent NFT purchase for $69 million which garnered significant media coverage was even publicly known to have been someone that already had a prior business relationship with the seller. Regardless, it seemed to have made a good enough story to make it to just about every ‘news’ website – which was exactly the intention of this purchase

Q: Why do you hate cryptocurrencies or Ethereum so much? You must be a fiat supporter!

A: I don’t hate cryptocurrencies at all; I actually love the concept of many of them and think ideas like Bitcoin and Ethereum have been revolutionary. I own Bitcoin, Ethereum, and Polkadot, and enjoy using them. I do kind of support fiat, however, so you might have me there; my need to pay bills and taxes is unfortunately not circumventable right now.

Q: How can I learn more about how NFTs are marketed?

A: This video is my favorite single resource to show someone who would like to learn how they can get rich quick by copying the well-known methodologies of the pros. This video is not about cryptocurrencies, but you’ll find that the common tactics of market manipulation work just as well in cryptocurrency markets as they do in traditional finance.

There’s many tactics commonly used that are not mentioned in this video as well, including purchasing social media interaction (Twitter followers, retweets, Discord server members, Reddit posts, Reddit upvotes, many others), having multiple levels of insiders who get stakes in projects before anyone else does and then consequently hype them up, purchasing press releases and news article about projects encouraging positive price action with forward-looking statements, wash trading and painting the tape in order to increase the perceived price and price increase of items (things like this may even be outsourced or fully automated. There’s money to be made, after all), copying art and code from others in order to quickly seek a profit with even less original work, and in general many other forms of fraud, of which the goal is to convince users that they will make money when engaging in actions that have specifically been designed to enrich parties other than themselves, often where said other parties are 1) significantly more well-versed in the workings of cryptocurrencies and the markets they are operating in, as well as 2) acquired their NFTs/coins/tokens/DefinitelyNotSecurities at significantly lower prices far before most other users were able to, and thus stand to gain asymmetrically better risk and reward for their activities, which generally consist of marketing in every shape and form imaginable, no matter how annoying or fraudulent (hence NFTs being an inherently viral phenomenon – there is no better way to artificially induce a high R0 in a meme than to directly incentivize it via rewarding large profits to those who are the most effective at spreading it).

Comments on Firefox

This post is a summary of some of the things that I dislike about Mozilla and Firefox. Given how passionate I am about user rights, privacy, decentralization, FOSS, etc, sometimes these remarks surprise people. I still am grateful Mozilla exists, I still use some of their products, and there are many amazingly smart and good people there However, donations to Mozilla for the purpose of improving Firefox are ineffective and are better spent elsewhere, and I really wish they would stay focused on making better products.

Mozilla has a lot of money, most of which does not go towards Firefox

Mozilla constantly mentions that they are a nonprofit, encouraging you to donate to them to help Make The Internet A Better Place. While the Mozilla Foundation is legally classified as a nonprofit, their subsidiary, Mozilla Corporation, is not. Its revenue is around $450,000,000 per year, almost all of which comes from their contracts with Google (Yandex and Baidu as well). Google pays Mozilla half a billion dollars per year because Mozilla has contractually agreed to keep Google as their default search engine, and presumably this gives Google a net profit, as having more ad views and user information is very, very valuable (I heard an explanation that Google also wants to avoid antitrust issues, but I’m unsure of the veracity of that).

The CEO of Mozilla (both the foundation and the corporation), Mitchell Baker, had an annual income of over $3,000,000 (official source, cannot find 2020 document yet) or around $1,000/hour, which has managed to increase for several years in a row, despite metrics related to Mozilla’s primary product, their web browser, significantly decreasing (do note: her salary is technically from the for-profit, not the non-profit). In case you haven’t seen a report on browser market share in the last few years, Firefox currently has around 3-4% of the market share, with the highest estimates I can find being around 7-8%.

Yeah, it’s kinda bad

Most of Mozilla’s spending does not go to software development nor Firefox, but rather to administration, marketing, and similar expenses (this is true both for the non-profit and for-profit, but the non-profit’s information is publicly available). Checking their most recent form 990, there was $4.5M spent on grants to random universities and groups, $3M spent on management fees, $1.8M spent on travel fees, and $0.8M spent on conference fees, which combined is significantly more than what is spent on employee compensation. This means when you donate to Mozilla’s nonprofit, your money is more likely to be spent on universities, management, and travel than an employee’s compensation.

Although there are not many publicly available details about the specific spending of the for-profit section of Mozilla (which would be ~10x more), the distributions appear to be relateively similar from what sources I can find. One reason why Mozilla spends so much on marketing is because their products are generally not as good as their competitors’, and attempting to purchase your way to a larger userbase is an expensive and constant uphill battle.

Firefox does little to stop you from being tracked by Google

One of the most popular reasons to use Firefox instead of Chrome is a dislike for being tracked by Google. While it’s true that Google recieves more information from Chrome users than it does from Firefox users, the majority of information flow remains a constant, and Mozilla relies on a plethora of Google services for basic browser functionality. Here are some examples:

  • Firefox uses Google search by default and sends all queries/address bar typing to Google
  • Firefox uses Google’s safe browsing service for ‘unrecognized downloads’, sending Google the filename and url that you visited
  • Firefox uses Google services for basic APIs such as their location API, despite Mozilla having attempted its own implementation, which one may assume they’d use. As Firefox polls your OS for information to send to this API, this sends information such as your wifi-network or nearby phone towers in addition to your IP address and a biweekly-rotating Google client identifier.

Apart from Firefox relying heavily on Google’s services, unless you use extensive tracking/blocking addons, you’re being tracked everywhere you go to begin with, as the majority of websites use Google Analytics, Google APIs, Google fonts, Google ReCAPTCHA, among many others.

There is truth to Mozilla working on and implementing important privacy improvements in browsers, such as DNS over HTTPS, third party cookie blocking by default, tracker blocking, and so on. Some of these appear to be helpful, however are easily mitigated by other parties, while others are more questionable (for example, the implemention method of rolling out DoH by opting users into it, bypassing their network configuration preferences, and sending all DNS queries to a single company’s servers, was not optimal). As of firefox 86 on Feb 23rd 2021, Firefox appears to be attempting full per-site cookie isolation, which if successful and usable could be a great improvement here.

Firefox includes tracking, advertisements, and backdoors

Mozilla takes almost every chance it can to tell you how much they love your privacy, and for that reason the tracking and default features that are included in distributions of Firefox are pretty surprising (this does not mean Firefox is worse at this than other browsers!).

By default, firefox shares all of the following with Mozilla:

– the number of open tabs and windows, the number of websites visited, the number and type of addons installed, the length of your browser session, all interaction events with ‘Firefox features offered by Mozilla or our partners’, your device information, OS information, hardware information, and your IP address

  • “Firefox uses your IP address to suggest relevant content based on your country and state”
  • “When you choose to click on a Snippet link, we may receive data about the link you followed”
  • “Firefox sends basic information about unrecognized downloads to Google’s SafeBrowsing Service, including the filename and the URL it was downloaded from”

Some of this information is reasonable, such as crash reports and the base OS/Firefox version, but I still found this to be more than many may expect.

Firefox now comes with a feature called studies, which allows Mozilla to remotely install and run custom changes and featuresets to your browser without asking you. This is turned on by default, which is generally all that matters as almost no users go through every setting in software to turn things off manually. In the past Mozilla used their ability to remotely control browser installations to install an addon into users’ browsers that gave them cryptic messages which were intended to be advertising for a TV show. I don’t know why they thought that was a good idea, as it seemed to be almost unanimously agreed upon that it was a terrible idea, but it still happened. If you visit about:studies in Firefox you can see which studies you have/are currently participating in. I could not find any resource from Mozilla that lists all studies that they run, or anything remotely like this.

Firefox continually pushes sponsored and clickbait content into their products

Firefox comes with many features for sponsored content and advertisements, such as Sponsored Top Sites. The Mozilla page about this feature says they send ‘anonymized technical data’, which is hyperlinked to a near-empty Github repositry. Firefox partners with adMarketplace for this, which states “We may also receive technical information such as your approximate location, browser type, language settings, user agent, timestamp, cookie ID and IP addresses”, which is very dissimilar to what Mozilla says about this tracking, but perhaps they have a special agreement with Mozilla to opt their users out of this or something.

There is also Pocket, which comes with all distributions of Firefox and shows sponsored stories and other content ‘curated by our editors’ by default. I’m not even going to pretend this is decent. This is is a terible feature, and the last thing I want to see when I open my web browser is a bunch of advertisements for clickbait. I find it sad that mozilla says Pocket “Trades clickbait for quality content”, when the majority of content Pocket offers is complete trash designed to make you click and waste your time, including a lot of content that suggests that surveillance and censorship of the Internet is required to keep me informed and safe.

Please keep your clickbait out of my browser’s default home page, thank you

Fortunately several of the worst features of Firefox are easy to turn off, and some features that are even worse such as Ion, which literally just sends your browsing history to ‘researchers’, are disabled by default and must be opted into. I’m unsure why these features are included in Firefox to begin with, as I can’t imagine the small revenue stream they introduce is significant nor in Mozilla’s best interest.

Firefox is generally a slower browser than Chrome

If you’re a Firefox user, I suggested using Chromium just for a few minutes. I usually use forks of Firefox or Firefox ESR, but when I use Chromium I’m sometimes stunned at how much faster it is. Finding fair and recent browser benchmarks is difficult, but but most of which I’m able to find seem to confirm this, and testing local website rendering myself results in Chrome not just being slightly faster, but often 50-300% faster with its rendering, network requests, and javascript execution.

Using Chrome for a few minutes instantly allows me to understand why it has dominated Firefox in market share over the last decade. While it’s true that Google has many inherent advantages in promoting software, I think its performance, speed, and UX alone goes a long way in demonstrating why Firefox has fallen behind so far.

Mozilla has strange and contradictory ideological goals

When visiting the homepage mozilla.org, the first article that is shown to me is titled ‘We need more than deplatforming’ written by the CEO Mozilla, which implores us to do things like “Turn on by default the tools to amplify factual voices over disinformation”, kindly linking us to a NYT article that discusses how ‘authoritative sources’ such as the NYT and CNN should be prioritized over independent voices.

I don’t want to write much about politics for reasons that should be obvious, but attempting to solve the world’s problems via fact-checking is terrible naive and has no chance of working out well, and I’m amazed at how many large organizations seem to act like the solution to our society’s problems is for us to just ask a fact-checker what is true and what is false, and then hold hands and sing songs as our new utopia is formed.

Continuing to read blogposts from Mozilla (this is from their foundation’s website, I should add that they have some good technical blogposts in other locations) is a rather interesting endeavor as it becomes more and more apparent that Mozilla has large segments of their organization that don’t seem to have any clear goals, and just kind of write about random social and political things on the Internet and their opinions on it, sometimes throwing six-figure grants to random groups of students to make a game that no one ever plays to show us about how something is obviously bad, which I assume they thought was a better use of their money than hiring someone to work on Firefox (which 250 people were laid off from last year).

While Mozilla attempts to provide commentary on many important social issues, there appear to be many suggestions that go directly against their manifesto, which suggests that open expression and individuals freedoms should be prioritized. I respect the right for Mozilla to spend its funding on any social or political content it chooses, and I also think that many of the issues they dedicate time to are very important for our society and for the Internet, but I would rather their organization focuses on making a good web browser, because I would be much more excited about donating to them if my money went towards that.

I’m still glad Firefox exists

I’ve written some negative views about Firefox, but I’m still glad it exists. Making a perfect web browser is difficult, and trying to respect user privacy is difficult. I think Mozilla would be much better off if they were a product-focused company, and spent more money on technical innovation and additional engineers and innovators. For this reason I don’t think donating to Mozilla is a good choice, and as far as similar organizations go, prefer the EFF instead.

This article started to turn into a bit of a rant as I’ve continually found myself disappointed with decisions Mozilla has made, and I’m not surprised that their browser market share has decreased by almost 90% over time as a result. It’s easy to criticize, but difficult to build, so I do want to include this disclaimer to restate that I’m glad Firefox and Mozilla exist, and I wish the best for them and their browser, but I think their modern directions are distracting them from making products good enough to be widely used. I hope things improve, because it would be nice if more than one or two web browsers existed. In fact, I think that’s very important.

This Anime Does Not Exist

This Anime Does Not Exist was launched on January 19th 2021, showcasing almost a million images (n=900,000 at launch, now n=1,800,000 images), every single one of which was generated by Aydao‘s Stylegan2 model. For an in-depth write-up on the progression of the field of anime art generation as well as techniques, datasets, past attempts, and the machine learning details of the model used, please read Gwern’s post. This post is a more concise and visual post discussing the website itself, thisanimedoesnotexist.ai, including more images, videos, and statistics.

The Creativity Slider and Creativity Montage

Previous versions of ‘This X Does Not Exist’ (including anime faces, furry faces, and much more) featured a similar layout: an ‘infinite’ sliding grid of randomly-selected samples using the javascript library TXDNE.js, written by Obormot. Something more unique about Aydao’s model was that samples remained relatively stable, sometimes significantly increasing in beauty and detail as the ‘creativity’ value (see: psi) was increased all the way from 0.3 to 2.0. This led to the creation of the ‘creativity slider’ as well as linking every image to a page with a tiled layout showing every version of the image:

“The more entropy you give me, the more it makes me want to smile!”, 18 samples of image # X from creativity 0.3 to 2.0
One of the best and most common effects of higher creativity is better colorization, including shading, reflections, vibrancy, color diversity, and more
Another tile of seed 7087, showcasing stability with an increasingly interesting artistic style and details

Although the above two are among my favorite examples of creativity montages, many users found some other interesting things that increased creativity could do:

Sometimes it appeared as if ‘creativity’ was simply an alias for the increase in volume of a certain bodily area coupled with a proportional reduction of garment-covering surface area (seed 30700)
Sometimes increased creativity also leads to mitosis (seed 28499)
Sometimes you get… a lot of mitosis?

Selected artwork

The best way to demonstrate the stunning potential of this model is to show some of the samples that users have enjoyed the most:

The original thumbnail image for This Anime Does Not Exist: “Notice me, Onee-chan!”
Other earlier candidates considered for the website’s thumbnail (seeds: 1013, 4606, 8674, 8859)
Four popular images selected by Twitter users
Images from seeds 16736, 23655, 62731, and 93887
Images from seeds 84995, 50428, 10157, and 52476

Weirdest images

Incidentally, it also seems that users love sharing images that are not the most beautiful, but the weirdest as well. The below four were among the most popular images on the website during the first few hours, when there was only n=10,000 of each image:

A montage of the interesting and popular results from images 3313, 7820, 4437, and 3103. Sample 3103 would be a particularly good album cover for a death metal band.

Collapsed images

Sometimes the result collapses enough to lead to an image that, although pretty, does not at all resemble the ideal target:

interesting but unintended results from samples 0544, 31975, 3997, 0557

Writing

In many cases the model will produce writing which looks distinctly Japanese, however upon closer introspection, is not legible, with each character closely resembling distinct counterparts in Japnese scripts, however diverging just enough to produce confusion with a lingering feeling of otherworldlyness.

Although some characters are easily recognizable, many are not, and are nonetheless *usually* combined in incoherent manners

Videos and gifs

As it’s possible to produce any number of images from the model, we can also use these images to produce videos and animated gifs. The primary style of this is referred to as an interpolation video which is produced by iterating through the latent variables frame by frame, transitioning in between different samples seamlessly:

Interpolation video produced by arfa

Additionally, I decided to make a few videos that used a constant image seed, but modified only the creativity value instead (instructions on how I did this are here):

I chose this particularly wholesome sample to demonstrate a gif with creativity 0.3-2.0 and a frame difference of 0.01

Statistics and users

After the first day, the website had served over 100 million requests, using over 40TB of bandwidth:

First-day traffic statistics from CloudFlare’s Traffic Analytics

At launch, the largest contributor to traffic by country was the United States, followed by Russia, but over the next two days this quickly shifted to Japan.

A map showing which of Cloudflare’s data centers served the most DNS query results for the domain

As of writing this post (Jan 21st, 2021), the largest sources of traffic appear to be from Twitter, Hacker News, Gigazine, Hatena, and Himasoku.

Costs

Compare to similarly-trafficed websites, thisanimedoesnotexist.ai was relatively cheap, thanks to not requiring server-side code (serving only static content):

  • Domain ‘thisanimedoesnotexist.ai’: for two years from NameCheap: $110

  • Cloudflare premium, although not required, improves image load time significantly via caching with their global CDN: $20

  • Image generation: 1,800,000 images, 10,000 generated per hour with a batch size of 16 using a g4dn.xlarge instance, which has a single V100 GPU with 16GB of VRAM at $0.526 per hour on-demand: $95

  • “Accidentally” hosting the website from AWS for the first day, resulting in over 10TB of non-cached bandwidth charges: >$1,000 (via credits)
An image of what my desktop looks like while generating an additional million anime images
What the access log for nginx looks like while serving >1,000 anime images per second
Yet another example of why to not use AWS for high-bandwidth content: AWS has some of the most expensive bandwidth at $0.09 per GB (luckily this was paid for entirely with credits and the migration off of AWS was complete in less than a day to a more sustainable provider)

Conclusions and the future

All in all, this was a fun project to put together and host, and I’m glad that hundreds of thousands of people have visited it, discussed it, and enjoyed this novel style of artwork.

If you want to read in-depth about the ML behind this model and everything related to it, please read Gwern’s post.

Thank you to Aydao for relentlessly improving Stylegan2 and training on danbooru2019 until these results were achieved as well as releasing the model for anyone to use, Obormot for the base javascript library used, TXDNE.js, Gwern for producing high-quality writeups, releasing the danbooru datasets, and and other members of Tensorfork including Gwern, arfa, shawwn, Skyli0n, Cory li, and more.

The field of AI artwork, content generation, and anything related is moving very quickly and I expect these results to be surpassed before the year is over, possibly even within a few months.

If you have a technical background and are looking for an area to specialize in, I cannot emphasize the extent that I’d strongly suggest machine learning/artificial intelligence: it will have the largest impact, it will affect the most fields, it will help the most people, it will pay the most, and it will cause you to be surrounded by the best and smartest people you could hope for.

Thanks for reading and I hope you enjoyed the website! For more about myself, feel free to read my about page or see my Twitter.

Bonus: additional image compilations from Gwern

Quotes from The Everything Store – Jeff Bezos and the Age of Amazon

The Everything Store – Jeff Bezos and the Age of Amazon by Brad Stone is a book detailing some factors that led to the rise of Amazon as one of the largest corporate success stories of all time. I opened it expecting to skim through some parts, but ended up reading it in full in one sitting, and enjoyed it thoroughly. It left me with a strong sense of what makes Amazon, well, Amazon. And the best answer to that question is without a doubt, Bezos himself.

Rather than a full book review, I’m going to share some quotes from The Everything Store that stood out to me. One fun thing to note is that when this book was published in 2013, Amazon was ‘only’ a $150B company, but today is worth over 1.5 trillion. It’s a wonderful book and is worth buying if you want to read stories about Jeff Bezos’ extreme confidence in himself and his company as they overcome challenges one after another full-speed ahead, from local stores to Barnes and Noble to Ebay to Walmart and beyond. Below are some quotes that I particularly liked, only from the first fourth of the book. I was quoting the book more than anticipated, so I stopped this post early but will leave it up as an advertisement for the book.

Bezos is an excruciatingly prudent communicator for his own company.
He is sphinxlike with details of his plans, keeping thoughts and intentions
private, and he’s an enigma in the Seattle business community and in the
broader technology industry. He rarely speaks at conferences and gives
media interviews infrequently.

There is so much stuff that has yet to be invented.
There’s so much new that’s going to happen.
People don’t have any idea yet how impactful the Internet is going to
be and that this is still Day 1 in such a big way.
Jeff Bezos

Amazon’s internal customs are deeply idiosyncratic. PowerPoint decks
or slide presentations are never used in meetings. Instead, employees are
required to write six-page narratives laying out their points in prose, because
Bezos believes doing so fosters critical thinking. For each new product, they
craft their documents in the style of a press release. The goal is to frame a
proposed initiative in the way a customer might hear about it for the first
time. Each meeting begins with everyone silently reading the document, and
discussion commences afterward

“If you want to get to the truth about what makes us different, it’s this,”
Bezos says, veering into a familiar Jeffism: “We are genuinely customer-
centric, we are genuinely long-term oriented and we genuinely like to invent.
Most companies are not those things. They are focused on the competitor,
rather than the customer. They want to work on things that will pay
dividends in two or three years, and if they don’t work in two or three years
they will move on to something else. And they prefer to be close-followers
rather than inventors, because it’s safer. So if you want to capture the truth
about Amazon, that is why we are different. Very few companies have all of
those three elements.”

Bezos interpolated from this that Web activity overall had gone up that year by a factor of roughly 2,300—a 230,000 percent increase. “Things just don’t grow that fast,” Bezos later said. “It’s highly unusual, and that started me thinking, What kind of business plan might make sense in the context of that growth?”

Jackie Bezos suggested to her son that he run his new company at night or on the weekends. “No, things are changing fast,” Bezos told her. “I need to move quickly.”

Internet records show that during that time, they registered the Web domains Awake.com, Browse.com, and Bookmall.com. Bezos also briefly considered Aard.com, from a Dutch word, as a way to stake a claim at the top of most listings of websites, which at the time were arranged alphabetically.

Bezos and his wife grew fond of another possibility: Relentless.com. Friends suggested that it sounded a bit sinister. But something about it must have captivated Bezos: he registered the URL in September 1994, and he kept it. Type Relentless.com into the Web today and it takes you to Amazon.

They set up shop in the converted garage of Bezos’s house, an enclosed space without insulation and with a large, black potbellied stove at its center. Bezos built the first two desks out of sixty-dollar blond-wood doors from Home Depot, an endeavor that later carried almost biblical significance at Amazon, like Noah building the ark.

During that time, the name Cadabra lived on, serving as a temporary placeholder. But in late October of 1994, Bezos pored through the A section of the dictionary and had an epiphany when he reached the word Amazon. Earth’s largest river; Earth’s largest bookstore.3 He walked into the garage one morning and informed his colleagues of the company’s new name. He gave the impression that he didn’t care to hear anyone’s opinion on it, and he registered the new URL on November 1, 1994. “This is not only the largest river in the world, it’s many times larger than the next biggest river. It blows all other rivers away,” Bezos said.

One early challenge was that the book distributors required retailers to order ten books at a time. Amazon didn’t yet have that kind of sales volume, and Bezos later enjoyed telling the story of how he got around it. “We found a loophole,” he said. “Their systems were programmed in such a way that you didn’t have to receive ten books, you only had to order ten books. So we found an obscure book about lichens that they had in their system but was out of stock. We began ordering the one book we wanted and nine copies of the lichen book. They would ship out the book we needed and a note that said, ‘Sorry, but we’re out of the lichen book.’

A week after the launch, Jerry Yang and David Filo, Stanford graduate students, wrote them an e-mail and asked if they would like to be featured on a site called Yahoo that listed cool things on the Web. At that time, Yahoo was one of the most highly trafficked sites on the Web and the default home page for many of the Internet’s earliest users.

In the meetings, Bezos presented what was, at best, an ambiguous picture of Amazon’s future. At the time, it had about $139,000 in assets, $69,000 of which was in cash. The company had lost $52,000 in 1994 and was on track to lose another $300,000 that year. Against that meager start, Bezos would tell investors he projected $74 million in sales by 2000 if things went moderately well, and $114 million in sales if they went much better than expected. (Actual net sales in 2000: $1.64 billion.)

Bezos later told the online journal of the Wharton School, “We got the normal comments from well-meaning people who basically didn’t believe the business plan; they just didn’t think it would work.”11 Among the concerns was this prediction: “If you’re successful, you’re going to need a warehouse the size of the Library of Congress,” one investor told him.

When his goals did slip out, they were improbably grandiose. Though the startup’s focus was clearly on books, Davis recalls Bezos saying he wanted to build “the next Sears,” a lasting company that was a major force in retail. Lovejoy, a kayaking enthusiast, remembers Bezos telling him that he envisioned a day when the site would sell not only books about kayaks but kayaks themselves, subscriptions to kayaking magazines, and reservations for kayaking trips—everything related to the sport. “I thought he was a little bit crazy,” says Lovejoy.

The IPO process was painful in another way: During the seven-week SEC-mandated “quiet period,” Bezos was not permitted to talk to the press. “I can’t believe we have to delay our business by seven years,” he complained, equating weeks to years because he believed that the Internet was evolving at such an accelerated rate. Staying out of the press soon became even more difficult. Three days before Amazon’s IPO, Barnes & Noble filed a lawsuit against Amazon in federal court alleging that Amazon was falsely advertising itself to be the Earth’s Largest Bookstore. Riggio was appropriately worried about Amazon, but with the lawsuit he ended up giving his smaller competitor more attention. Later that month, the Riggios unveiled their own website, and many seemed ready to see Amazon crushed. The CEO of Forrester Research, a widely followed technology research firm, issued a report in which he called the company “Amazon.Toast.”


It was a distilled version of the dissatisfaction felt by many early Amazon employees. With his convincing gospel, Bezos had persuaded them all to have faith, and they were richly rewarded as a result. Then the steely-eyed founder replaced them with a new and more experienced group of believers. Watching the company move on without them gave these employees a gnawing sensation, as if their child had left home and moved in with another family. But in the end, as Bezos made abundantly clear to Shel Kaphan,family. But in the end, as Bezos made abundantly clear to Shel Kaphan, Amazon had only one true parent.

“You seem like a really nice guy, so don’t take this the wrong way, but you really need to sell to Barnes and Noble and get out now,” one student bluntly informed Bezos. Brian Birtwistle, a student in the class, recalls that Bezos was humble and circumspect. “You may be right,” Amazon’s founder told the students. “But I think you might be underestimating the degree to which established brick-and-mortar business, or any company that might be used to doing things a certain way, will find it hard to be nimble or to focus attention on a new channel. I guess we’ll see.”

“There will be a proliferation of companies in this space and most will die. There will be only a few enduring brands, and we will be one of them.”

During that time, no one placed bigger, bolder bets on the Internet than Jeff Bezos. Bezos believed more than anyone that the Web would change the landscape for companies and customers, so he sprinted ahead without the least hesitation. “I think our company is undervalued” became another oft- repeated Jeffism. “The world just doesn’t understand what Amazon is going to be.”

As the company grew, Bezos offered another sign that his ambitions were larger than anyone had suspected. He started hiring more Walmart executives.

Around that time, Wright showed Bezos the blueprints for a new warehouse in Fernley, Nevada, thirty miles east of Reno. The founder’s eyes lit up. “This is beautiful, Jimmy,” Bezos said. Wright asked who he needed to show the plans to and what kind of return on investment he would have to demonstrate. “Don’t worry about that,” Bezos said. “Just get it built.” “Don’t I have to get approval to do this?” Wright asked. “You just did,” Bezos said. Over the next year, Wright went on a wild $300 million spending spree.

“Walmart did not even have Internet in the building back then,” says Kerry Morris, a product buyer who moved from Walmart to Amazon. “We weren’t online. We weren’t e-mailing. None of us even knew what he meant by online retail.”

The venture capitalists backing eBay asked around and heard that one did not work with Jeff Bezos; one worked for him.

Bezos went skiing in Aspen that winter with Cook and Doerr and finally told them what was coming. “He said, ‘We’re going to win, so you probably want to consider whether to stay on the eBay board,’ ” says Cook. “He thought it would be the only natural outcome.”

If you liked these quotes, consider reading the full copy (perhaps even buying it from Amazon), it’s definitely a nice read about an amazing company and individual.

The Twitter Hack Could Have Been Much Worse

Midday on July 15th, 2020, many high-profile Twitter accounts were compromised and began posting scams to entice users into sending them cryptocurrency (generally BTC, but also some others such as XRP for Ripple’s account). I’m not going to write about this in detail since everyone else already has, but for more information check out an article on the topic: Coindesk, TheVerge, TechCrunch, BBC, infinite others

What if instead of posting low-quality cryptocurrency scams, the attackers did something else?

Sure, they could have tried to use CEO accounts such as Musk and Bezos to make millions (or possibly billions) on the stock market by tweeting about earnings and purchasing large amounts of far-out-of-the-money near-expiration call options on the underlying stocks. But we have a lot of ways to catch people that try that, and many regulations and organizations that would make it more difficult (many more than just the SEC) to get away with (although as a side note, $TLSA’s stock+option trading volume is absurdly high, and it would be very difficult).

But, what if they had tried something else entirely, something not motivated by short-term financial gain?

What if the attackers wanted to cause chaos and violence, perhaps alongside putting certain political movements and goals forward? What if they had pre-written thousands of tweets about a topic, perhaps a fake and outrageous event occurring, paired with fake images and videos, perhaps even some higher-quality deepfakes? How many people could they get killed? Could they start a war?

You might think this sounds absurd at first glance. But remember, most of the world’s most influential people use Twitter, including the leaders of most national governments. Although a private corporation that plays by its own rules, Twitter is still the means with which many elected officials communicate with the public. Entire social movements have started and ended through the power of a single viral tweet, sometimes resulting in significant violence or many deaths. Social media platforms have been used by extremists of every type imaginable in the past, and this isn’t going to stop any time soon.

What if the next exploit affects much more than some Twitter accounts?

But, I want to go much further than talking about Twitter. What if instead of an exploit that allowed attackers to compromise Twitter accounts, it had been something much worse? What if they were able to compromise any web server, or any online Windows machine, or industrial control systems for utilities, power plants and military operations? None of these scenarios are by any means impossible. Enough software and hardware exists at enough layers of abstraction that there’s generally always 0-days lurking in critical systems, sometimes for years or decades, before they’re found. We know that 0days are found often by security researchers, private companies, governments, and others (sometimes rewarding up to $2,500,000), but also that they are less commonly exploited in obnoxious and harmful ways (generally being hoarded by government security agencies or reported in good faith).

We were unprepared for covid despite epidemics throughout all of history

It was said by many that the covid pandemic could have been predicted, in a sense (which is why it was not a true black swan event). Perhaps not the specifics of it such as the date, virus, and origin. But the general idea of “at some point in the future, something bad is going to happen like this, and we need to prepare for it.”

Another one of these “something really bad is going to happen in the future” categories involves cybersecurity, data privacy, and AI. Just one of these topics individually can be involved in a terrible catastrophe, and indeed have been before, but I think we’re coming close to a combination of all three that can lead to events much worse than we’re currently prepared for.

Security: Billions of humans live digital lives, including the most influential, famous, and dangerous. These people all have email accounts, phones, Twitter accounts, and more, all of which can be compromised, controlled, and manipulated by others.

Data Privacy: The amount of data that social media giants (among others) have on most people is massive, and in my opinion vastly underestimated both in quantity and power. The majority of human communication is now owned by private companies that store things forever. A large proportion of all human social connections, conversions, movements, opinions, and thoughts are stored in databases that not only will not forget, but that the user does not have any control or often even knowledge of.

AI: Advances in the area of content generation have been happening very quickly in the last few years. We now have GPT-3, which can write plenty of things better than humans can. We have deepfakes, which can produce believable fake images and videos. We can do the same for voices and much more. Much of this isn’t yet perfect, but it’s clear that we’re improving quickly.

So, take the three above topics of security, data privacy, and AI, and combine them all. Bonus points if you throw in some political tension, which we’re certainly not lacking right now either.

We are not prepared for a true disaster involving technology

As a society, we’re woefully under-prepared for disasters in all of these areas.

We’re not prepared for critical infrastructure, both physical and digital, to be compromised or attacked by highly-funded and competent groups, maybe even state-ran.

Not prepared for the massive campaigns of disinformation, fake news, and propaganda that lie ahead. If you thought things were bad in the last few years, just wait, because we’re on the verge of accelerating it by 10x, and fact-checking is not a solution. China’s government seems to be working very hard both on the offensive and defensive here. Is anyone else truly competing?

Not prepared for how to deal with database leaks that will contain the life history of millions of people, including their ‘private’ conversations and deepest secrets, and items so egregious that they instantly spark violence. Plenty of data breaches have led to murders and suicides already. There are still many countries where you can face imprisonment or death for being gay, being atheist, being of a certain ethnicity, or speaking out against the government (yes, we really don’t have it as bad here, huh!). Do you know what happens when these people have their private information carelessly leaked? It’s not pretty. And this is just for normal database leaks, let alone if a database leak had some information in it falsified (with the majority left intact, thus offering plausibility for the fake parts) to maximize its effect.

Not prepared for how to face that humanity is becoming increasingly controlled by viral algorithms that do not prioritize human values of happiness and love and truth, but rather nothing but outrage and in-group bias as the only bottom line. Most of us already feel powerless against this, but it may only just be beginning.

Not prepared for how anonymity is becoming a luxury only achievable by ultra-competent tech gurus, with most people having been forced to move their communication into more and more centralized ways over time, feeding all of the above issues. Not prepared for how one of the many reasons anonymity is getting much more difficult to obtain is because the easiest way to tell if someone is a bot or a human is to require verification of phone numbers, addresses, and more. And don’t let me forget to mention how many governments are eyeing up ways to ban end-to-end encryption.

I’m supposed to end on an optimistic note

How can we do a better job of addressing these problems?

  • Promote education on the importance of cybersecurity, especially at the government and corporate levels
  • Promote decentralized solutions instead of centralized social media platforms, allowing users to have control over their discourse, their platform, and their own data
  • Promote anonymity, even when it is difficult, and fight to ensure end-to-end encryption is a right for everyone forever
  • Promote better regulations around privacy and data security so that hoarding large amounts of personal data is less of an asset and more of a liability

Although a lot of this post might read as alarmist and pessimistic, I’m still (mostly) optimistic about these things in the long-long-term. The best part about terrible events like covid is that they make us stronger and better prepared for the next (similar) storm to hit us. Security used to be a second thought (or not a thought at all) for most companies, but we’ve improved significant in the last decade, and bug bounty programs and significant security spending are now common. I used to get looked at like I was insane for talking about how big of an issue the amount of tracking and data-collecting our society performs was a big problem, but even this is something that a lot of everyday people believe now as well. I just hope the stepping stones along the way to becoming prepared for the future aren’t so terrible that we don’t make it there in one piece.

Feel free to say hi on Twitter for any comments, suggestions, complaints, etc.

Fact-Checking Is Not Easy

It’s interesting how many people view fact-checking as a simple problem, where you just identify something that is not factual, then correct it. Problem solved! Misinformation has been defeated, the Internet is only full only of Truth, and now The People finally realize we were right all along!

Fact-checking is a very hard problem. A lot of people want to ignore this fact, because correcting people feels good, especially when they’re your enemies.

It takes a lot of virtuousness, of empathy, of vigor, and of rationality to decline the temptation to correct other people. We are driven insane by the fact that not only are other people wrong on the Internet, but they are wrong about basic facts! This is part of why websites like Twitter are so terrible. People cannot stand others being wrong on the Internet. They will gladly spend hours of their daily life willfully being miserable and angry just to have the chance to correct others, even if those they correct do not even change their beliefs at all, or even change them in the opposite direction.

Humor aside, this is literally what fact-checking is

Although some may think the reason why Mark Zuckerberg has come out against fact-checking politicians is so that he can reap profits and sow division while cackling maniacally, I think instead he has simply put a lot of thought into the problem, and not only realized how difficult it is, but also that it cannot work well long-term. He is much more concerned about the long-term future (decades) of Facebook than he is about some upsetting posts made by an upsetting person.

Difficulties with fact-checking

I. There’s no such thing as an unbiased fact-checker

Fact-checkers, whether humans, scripts, or AI, cannot be unbiased. Reality is always a state of incomplete information, and the ways that humans interpret statements vary from person to person. It’s possible for us to disagree on the veracity of a statement, but if we were to discuss things further with more specificity, actually agree on the state of reality. Many statements can not reasonably be interpreted as a boolean of true or false, and instead have subtle amounts of potential bias and nuance within them. Facts are constantly changing, and no single actor has perfect and unbiased information about all of them.

II. Even if there was, someone has to decide which content should be fact-checked

Even given impossibly-perfect moderation, someone has to cherry-pick the content that is to be moderated and checked in the first place, as the Internet has far too much content to police every thought and post manually. Most individuals in favor of fact-checking tend to focus on a very small subset of individuals or organizations that they think should be fact-checked, but this set itself is cherry-picked according to their preferences and attention. This is another process that inevitably introduces bias, potentially in many directions depending on the people and processes involved. Similar to how two completely opposing news networks may only report true information, but still promote entirely opposing narratives because they cherry-pick what is news and what is not news, fact-checking cannot avoid this selection problem. It’s very unlikely that any large organization can do a reasonable job at this.

III. Even given quality fact-checking, the results may not be what you seek

A lot of people do not trust certain fact-checkers, certain news networks, and especially certain social media companies. Even if you perform good fact-checking, there is little evidence that this will achieve your goal, which is not actually correcting text on the Internet, but correcting peoples’ beliefs in their own minds, which turns out to be pretty difficult. Fact-checking could sometimes have an effect similar to the Streisand effect, potentially even causing harm to one’s cause, although I can’t find recent studies on this specifically. Regardless, it should be well-known by now that many people will not instantly and flawlessly change their minds when presented with new opposing facts, especially when done so by their outgroup.

If an Internet platform undertakes significant fact-checking, it could even drive heavily-affected groups off of the platform and onto their own platform, where they would then be even more free to spread their own information in whichever way they want. Similarly, the amount of trust that is given to many companies could decrease significantly and cause greater problems further down the road that can then not be solved with fact-checking.

Long-term affects of big changes are impossible to predict, but it’s not too hard to think about a lot of unintended consequences not just for social media, but for governments, democracy, and humanity, further down the road. Most people don’t have to try too hard to imagine some pretty dystopian results and major failure modes when trillion dollar corporations and governments become arbiters of truth and information.

IV. alternative narratives are important for society

Fact-checking has been desired and attempted by those in power throughout history, often leading to disastrous results, even without considering the political extremes of events such as WWII, which entire books of tragedy are written on. Many may view the Copernician revolution as ancient history, being 500 years ago, but it was only 170 years ago when Ignaz Semmelweis’ controversial hypothesis that doctors should wash their hands and maintain cleanliness was mocked and ridiculed for decades, until it eventually became common practice and saved millions of lives.

Lest those examples still appear as ancient history, remember that during the beginning of the covid pandemic, stating that covid was spreading from person to person directly contradicted the WHO (not to mention that everyone should wear masks, among others), and correspondingly would have been censored by platforms like Youtube according to their public policy.

History is full of countless examples of individuals that went against the grain of their encompassing culture in order to accomplish amazing things and drive progress. These people often armed themselves with what may have been originally considered to be misinformation by those in power during their zeitgeist. I’m glad that we didn’t have the centralization of communication and power we have now throughout history, because many rights that you take for granted were only gained thanks to the failures of past powers to control the narrative as strictly as they wanted to.

V. The narrative cannot be controlled

Just like everyone else, I too wish that everyone that was wrong on the Internet could be corrected. I wish my favorite narratives, facts, and causes were supported and known by more people. To not attempt to correct and control the narrative is a tough bullet to bite, but it’s something that a lot of thought and consideration must be put into, requiring very long-term thinking and awareness of history.

As long as people are free, they will come up with their own narratives, causes, desires, and even facts and entire worldviews. It’s been said that we live in a post-truth world, but that has always been the case. It’s just more apparent now that you can see people from every other background and culture when you use the Internet. No single person, company, or government can control information flow and peoples’ beliefs to the extent that they wish, and any that grasp for such an unattainable level of control will find that it doesn’t work long-term. Even the countries with the strictest controls on information, reporting, and speech, historically, have never fared well after a long enough time.

Different people have different lives, different values, and even different facts that they live by. It’s possible for you to co-exist with them, but perhaps not best if you’re forced to live in the same room as them. But no matter how hard you try, it may be impossible to get them to live their life the way you want them to. I know it’s difficult, but sometimes the only option is to let others live in their own world, while you live in yours, still helping to make it the best you can. Spending your days being angry and miserable on social media will not accomplish what you want, no matter how right you are.

Although this post might not be particularly insightful and is almost too political for my taste, I hope at the least this may help some realize that fact-checking is more difficult than it appears at first glance, even if they still support it.

I’m looking for more interesting people to chat with on Twitter, especially if you have corrections, improvements, or just like to discuss topics like longevity, startups, security, and finance, and more.

Supplements


Last updated: Oct 26 2024

This document is an updated list of most of the supplements/drugs that I take daily, as well as notes on some other interesting substances. It contains information on exactly what I take, how much of it, how much it costs, and some information on the substance which should roughly explain my reasons for taking it.

May 7th 2024 update: I have replaced many of the pills in this post (but not all of them!), with pills from Blueprint, although I don’t consume any of the auxiliary products. I would strongly suggest reading my post and review of Blueprint as it is now an essential addendum to this post. It saves quite a bit of management time as well.

The first list contains supplements I take daily, with the second list containing supplements that I do not take daily but that nonetheless seem interesting, while the third list contains supplements that are interesting, but that seem less suitable for safe human consumption or speculation. As of 2023, many supplements on my list have been discontinued, and this is mentioned next to the dosage.

The focus of my supplementation is to find substances that are both very safe and also have a notable probability of improving health, lifespan, well-being, or productivity, with the ultimate goal being to significantly slow aging, even if it’s difficult to do at this time. I don’t take many nootropics as I don’t think there’s much room for intelligence improvements just from ingesting simple compounds (evolution has already put quite a bit of time into making us smart), with the exception of treating some deficiency or other issue, or improving productivity/concentration, which definitely possible (see: caffeine, modafinil, adderall, many others), but distinct from intelligence. It is worth noting this list is very specific to myself: if I had a perfectly optimal diet and lifestyle, I would likely take next to zero supplements. Like most mortals, my diet and lifestyle are definitely not perfect (and indeed, even knowing what a perfect diet would be for yourself can be intractable on its own), thus there’s always room for improvement.

This post is not an attempt to convince anyone of something specific or to suggest anything specific, but I have decided to publish it publicly in order to better keep myself accountable for my reasoning, receive potential feedback, and to otherwise share some potentially useful short summaries of information. Concordantly, I’m not a doctor and this post contains no medical advice or suggestions. Which supplements, if any, one should take, is a very personal matter, as it is dependent upon many unique traits such as one’s age, diet, lifestyle, genes, risk preference, finances, and more.

Notes on supplements

Section tl;dr: most supplement marketing tactics, websites, videos, brands, etc, are bullshit. Do your own research, ask questions, and be quantitative.

Although there are a lot of supplements that would be beneficial to many people, caution must be exercised both with research and purchasing. Supplements in the United States have very little regulation, with some sellers having poor quality control, fraudulent research, marketing, claims, and poor ingredient composition and sourcing. The supplement industry is worth billions of dollars and has many bad actors incentivized by profit over truth, so time and care must be exercised in order to find out what works best for you personally. Certainly, research can be found promising positive effects from thousands of various substances – but taking all of them would be impractical, expensive, and likely downright harmful.

It’s also important to pay attention to brands as well as to think logically about which supplements have quality differentials that are worth paying more for. For example, Vitamin D and Glycine are easy to synthesize, and it’s likely that cheaper versions of these supplements are just as good as more expensive versions. This may not be the case for a supplement like fish oil however, which is derived from complex living organisms that vary significantly on factors such as their environment, diet, quality controls, the types of fish used, and so on.

Concordantly, one of the strongest criteria I look for in most supplements is safety, which many times (not always!) comes alongside popularity and/or significant research affirming the safety of compounds. As many supplements offer marginal benefits at best, it would be irrational to purchase and consume them if they had a good chance of causing harm, as this would easily cause them to fail a basic cost/benefit or risk/reward analysis (there’s definitely some cool compounds that have very high coefficients in both the numerator and denominator of their risk/reward ratio too, so careful decision making is required).

Ideally one should attempt to find quantitative measures to objectively evaluate if a substance is really helping them in the desired manner. In some cases this is both easy and cheap to do, for example with Vitamin D supplementation, which costs only a few cents a day, does not need to be compared to a placebo, and can be tested for in your blood for as little as $30. In other cases, proper testing is difficult or impossible and may require significant effort and time for very little benefit. Keeping one’s lifestyle, diet, and other factors a perfect experimental constant is certainly difficult, as is performing blind experiments on yourself, collecting and analyzing data, and finding the proper quantitative desideratum to test yourself on to begin with; testing if something specific has definitively made you slightly smarter, happier, healthier, more productive, or extended your lifespan, is certainly difficult if not occasionally impossible to do in a scientifically rigorous manner with a sample size of one.

Lastly, which supplements benefit an individual is a very personal matter. Vegans may want to take some supplements that are found in meat. Carnivores may want to take some supplements that are found in plants. Supplements that may benefit the elderly or those with common conditions such as hypercholesterolemia or diabetes often seem to be much less useful for otherwise healthy individuals. Indeed, for individuals that have many health conditions including the elderly, there’s significantly more that can be gained from supplementation, as there are many more problems that can be improved upon (although there are also be more risks as well). Supplements will effect someone differently depending on their weight, age, genetics, health, diet, and many other factors.

This means that it’s a bad idea to copy any individual’s routines completely, even if it’s a lot of work to do your own planning, research, and testing. It is also worth mentioning that the word ‘supplement’ is used here as a relatively generic word, simply meaning that the substance is only regulated as a food within the United States and thus requires no prescription (unless otherwise mentioned), but also offers few guarantees in terms of efficacy or consistency.

If you take 2 or more pills a day, the best pill organizer+dispenser by far is this (Image from Amazon reviews)

See also

If you find this page interesting, here are some similar pages from others that you may enjoy:

Supplements

Name: Vitamin D3

Dosage: 2,000+ IU (50+ µg, included in BP)

Cost/Day: $0.03

Information: Vitamin D3 [Examine, webmd, Wikipedia] (colecalciferol) is a vitamin made by the skin when exposed to sunlight. It’s a common deficiency and is very cheap to fix. The benefits of supplementation are generally found to be minor (it’s still a bit controversial if supplementation is beneficial at all, although I lean towards yes personally), but as I was notably deficient and it’s one of the cheapest supplements, it’s an easy choice for me. There is a lot of literature on Vitamin D, and many highly-powered studies including meta-analysis will often find only minor beneficial effects, but there are also quite a few studies that show notable benefits, including many related to covid as of late 2020. As noted above, this is also an easy supplement to receive a blood test for and ensure you’re taking the optimal dosage. I take half of my vitamin D earlier in the day without a meal, and the other half with my food, contrary to most other supplements. See also: Gwern on Vitamin D as well as on it harming sleep if taken at night

Name: Vitamin B6

Dosage: 1.4mg (included in BP)

Cost/Day: $0.04

Information: Vitamin B6 [Examine, webmd, Wikipedia]. This is included in other supplements I have and is otherwise not notable.

Name: Vitamin B12

Dosage: 125mcg (included in BP)

Cost/Day: $0.04

Information: Vitamin B12 [Examine, webmd, Wikipedia] (vitamin B3). This is included in other supplements I have and is otherwise not notable (although if you’re on metformin or a few others I used to try it’s better to add it, else unlikely to be deficient).

Name: Vitamin C

Dosage: 500mg

Cost/Day: $0.03

Information: Vitamin C [Examine, webmd, Wikipedia] (ascorbic acid) has a variety of effects, and being a vitamin, is an essential part of a human diet. I supplement vitamin C in order to fix a tested deficiency. I’m rarely deficient but it doesn’t hurt.

Name: Fish Oil

Dosage: 1-3g+ (depends on diet and estimated omega-6 intake)

Cost/day: $0.10 (1g)

Information: Fish oil [Examine, webmd, Wikipedia] (omega-3 EPA+DHA) is another common and cheap supplement. Although many studies find minor or sometimes no benefits, many others find a large amount of diverse improvements, even if they are minor. It’s likely that the ratio of omega-6/omega-3 you consume is important, with most people consuming far too much omega-6 (which won’t hurt to reduce regardless) and not enough omega-3, so dosing of fish oil should be based on your diet, which is easily more than an order of magnitude more important to begin with.

Similarly, it’s probably good advice to 1) reduce fried food intake, 2) replace oils high in linoleic acid such as safflower and sunflower oils with oils that have much less such as coconut oil and olive oil (2021 edit: I am less sure about this than I was before, although I still lean towards it myself Deciding which oils/fats (and with what / prepared in which manner) are bad for you continues to be an extremely hard problem. See A Comprehensive Rebuttal to Seed Oil Sophistry for an example of a comprehensive potential counter-argument in the great seed oil/fat debate) and 3) increase my supplementation of high-quality omega 3s (fish oil) when I think I’ve had more omega 6s. For example, if I do decide to eat a lot of fried food, I take several fish oils, compared to only 1-2g normally. I also like to note that fish oil seems to be one of the supplements worth spending a bit more money on – quality is high-variance and of higher importance, and unlike other supplements which can trivially be synthesized, the production processes of fish oil vary greatly depending on the company and product. Also see this review on pubmed and this summary on Wikipedia

Name: Garlic

Dosage: 1-3g (included in BP now)

Cost/day: $0.02 (1g)

Information: Garlic [Examine, webmd, Wikipedia] is another popular and cheap supplement. There’s good evidence that it improves lipid profiles, may help with some cancer risks, and may have other very minor benefits (may activate AMPK too?). The most desirable compound in garlic is allicin, which is diluted in garlic that is microwaved, boiled, or aged. Dosage should be based on which type of garlic is being consumed. As many people enjoy the taste of garlic, it’s a good candidate to include in meals as well (which is probably optimal for most things, resulting in notably higher bioavailability on average).

Name: Olive Leaf Extract

Dosage: 500mg (discontinued, decided it was too low-value)

Cost/day: $0.02

Information: Olive Leaf Extract [Examine, Wikipedia] is a cheap and easy way to hopefully mimic the benefits of olive oil, as the leaves of the olive tree contain good amounts of relevant olive phenols such as oleuropein. It may still be better to consume olive oil instead, which is still a great thing to add to meals, but with such a low cost, this seems worth inclusion to me. I am not particularly excited about this supplement but have included it regardless.

Name: Magnesium Citrate (replaced with magnesium glycinate)

Dosage: 250mg (magnesium glycinate: 1500mg)

Source: $0.05

Information: Magnesium [Examine, webmd, Wikipedia, Gwern] deficiencies are moderately common (up to 45-60%) and easily fixed. Fixing a magnesium deficiency is cheap and seems to offer quite a few minor general benefits, and also sleep and anxiety improvements for some. Depending on your diet, supplementation may be unnecessary. Magnesium comes in a lot of different forms so close attention is needed when purchasing. I stick to citrate as it makes dosing easier, has good bio-availability, and is unlikely to cause digestion issues. The above Gwern link is a great resource on Magnesium as well. This is also another supplement that is easy to get before and after blood tests for to see if your intervention performed as desired.

If you want to have both magnesium and glycine, magnesium glycinate can be purchased which contains both, generally in a ratio of ~14% magnesium to ~86% glycine. This can be a great supplement to take before bed.

Name: Vitamin K2 MK-7

Dosage: 100mcg (sometimes included in BP)

Cost/day: $0.00

Information: Vitamin K [Examine, webmd, Wikipedia], like most vitamins, is primarily beneficial for those deficient in it, so it is best to examine your diet thoroughly and/or be tested. There are several forms of vitamin K, and also several forms of vitamin K2. Vitamin K2 MK-7 seems to be one of the best forms to take in general, although K1 has decent evidence in favor of it as well, depending on one’s circumstances.

Name: Glucosamine Sulfate

Dosage: 1-3g (often paired with MSM, back on as of Oct 2024)

Cost/day: $0.19

Information: Glucosamine [Examine, webmd, Wikipedia] is an amino sugar derived from shellfish that is commonly taken by the elderly to improve joint functionality and reduce pain. Glucosamine extends the lifespan of some mammals in studies, potentially in ways that are evolutionarily conserved, activating AMPK and therefore having slight similarity with metformin. Glucosamine may also induce autophagy via an mTOR-independent pathway, which may be the mechanism of action for its effects on lifespan. Due to its popularity as a supplement we can be relatively sure of its safety as well. Chondroiton is commonly included with glucosamine supplements, which appears very uninteresting for my own purposes, so I look for pure d-glucosamine/glucosamine sulfate, which is generally cheap.

Name: Lithium Orotate

Dosage: 5mg (included in BP)

Cost/day: $0.08

Information: Lithium [webmd, Wikipedia] is a metallic element that is often found in foods such as legumes, grains, vegetables, and in some places, drinking water. Lithium is generally present in most diets in notable quantities, and in slightly larger quantities in diets such as the Mediterranean diet. For purposes such as mine, it is supplemented at low doses, which is much different (~1/100th the dose) from the doses sometimes prescribed for some psychiatric disorders. Lithium reduces mortality, stabilizes mood, and promotes longevity, likely via multiple pathways, although the specific mechanisms of action are difficult to discern and more research is needed. As I was tested for lithium and had a very low concentration in my blood, I decided it was worth it to supplement it n low doses.

Name: Glycine

Dosage: ~10g+

Cost/day: $0.20

Information: Glycine [Examine, webmd, Wikipedia] is an amino acid that is often supplemented to improve sleep. Better sleep is formidable by itself, but some studies find that it increases lifespan in organisms via methods that may be evolutionarily conserved. Although glycine is present in some foods and is also synthesized by your body, it may be the case that glycine deficiencies are technically common in humans, as the amount that is able to readily be synthesized in-vivo is sub-optimal. This may be relatively asymptomatic from an individual perspective and only manifest itself via a slight probabilistic decrease in healthspan/lifespan, although users often notice quite a few improvements besides just better sleep. Given its heavy involvement in collagen, I wouldn’t be surprised to see skin benefits over the long-term. Glycine may improve insulin sensitivity and other similar metrics. There may be some longevity benefits of a diet low in methionine (meat, fish, eggs, etc) as well, which may be related to one’s effective glycine/methionine ratio. I still consume a lot of methionine from common sources such as chicken breast, so this is another potential way in which glycine could be beneficial. Glycine appears to be very safe, even in larger doses, and is relatively cheap, more so as a powder, as is the case of most substances. See also Induction of glutathione biosynthesis by glycine-based treatment mitigates atherosclerosis

I often take glycine in powder form, which makes it easy to consume arbitrary doses (including the ability to add it to drinks or meals if desired), and notably cheaper than buying large amounts of pills, which are generally 1g each at most (you can’t fit more in a pill). On days where I consume a lot of meat such as beef, I take significantly more glycine. This is partially an attempt to optimize my diet’s methionine/glycine ratio, but also intended to do a better job at mimicking what a more traditional consumption of animal meat might have been like, from an evolutionary perspective, which would have included much more glycine than most of us receive in the common cuts of meat that consumers generally use. As a side note, glycine does taste sweet and dissolves in water, so it’s a great addition to tea or coffee.

Regardless, given glycine’s near-flawlessly safe and simple profile, there should be zero harm in having a bit too much. My larger dosage was arrived at from a combination of the papers linked above (and linked to by those links), as well as some reasoning about my diet (high in methionine) and lifestyle. Unfortunately even with a blood plasma test of amino acid concentrations, it’s difficult to know if this is the optimal dose for human longevity, or if it is even helpful at all to begin with, but the cost/benefit analysis here still seems to lean heavily into the green. As a simple and common amino acid, it seems pretty difficult to hurt yourself with glycine, so even taking 10-50g a day shouldn’t be harmful.

Name: Allulose

Dosage: 0-10g+ (varies, uncommonly used as a sweetener with some meals)

Cost/day: $0-0.50

Information: Allulose is an amazing alternative to sugar with 90% fewer calories and the ability to decrease your blood sugar in response to high-carbohydrate meals. I wrote a full post on Allulose here

Name: Bacopa

Dosage: 445mg (discontinued, likely low value)

Cost/day: $0.09

Information: Bacopa [Examine, webmd, Wikipedia] is an herb that seems to offer reliable but likely very minor improvements to some areas of memory and general cognition. Effects are likely difficult to notice without rigorous placebo-controlled self-testing, but it is relatively safe and cheap regardless. Digestive side-effects aren’t uncommon, as is the case with many herbal supplements. In the future I’d like to replace my bacopa with a placebo and attempt to look for differences in quantitative cognitive performance metrics such as my anki recollection, but performing this experiment well is difficult, both because the effect is very minor and because a proper experiment with n=1 is very difficult. I don’t think bacopa is likely to be a big deal, but I’ve added it for now. As of 2021 I sometimes don’t take this, as it may result in slightly poorer digestion, and the benefit was marginal at best, but I have left it on this list for now.

Name: Ashwagandha

Dosage: 470mg (occasionally discontinued due to potential digestive side-effects)

Cost/day: $0.15

Information: Ashwagandha [Examine, webmd, Wikipedia] is an herb that offers potential anxiety and lipid profile improvements. Some users report that it reduces anxiety and stress significantly, with some studies showing up to a 28% reductions in cortisol (in subjects with elevated levels). Lipid improvements can also be notable, with some studies showing a 10% reduction of total cholesterol, even in healthy subjects. As an uncommon herbal supplement, digestive side effects are a notable probability. Ashwagandha is likely worth trying if you feel that you have untreated anxiety, you never know when you’ll get lucky with how much of a benefit you receive from some things. Although not scientifically rigorous, it did appear like the periods during which I took ashwaganda resulted in a notably improved lipid profile, consistent with what many studies have shown. I’d like to test this on myself in an n=1 RCT both for lipids and for potential relaxation/anxiolytic effects, but haven’t gotten around to it.

Name: Fisetin

Dosage: 0-1500mg (varies, intermittently/rarely taken, but now included in BP at 100mg/day)

Cost/day: $0-3.80 (varies)

Information: Fisetin [Wikipedia] is a plant flavonol that is found in several vegetables and fruits, with the highest concentration being found in strawberries. Fisetin is a sirtuin-activating compound and has extended the lifespan of yeast, worms, flies, and mice. It has been shown to be a strong senolytic agent and may induce apoptosis and other effects via the PI3K/AKT/mTOR pathway. I do not take it every day and am quite uncertain about what the right regime for supplementation should be for it, but currently take ~1,500mg of it for 4 days continually once every few months. This likely has room for improvement and may change in the future. I’d like to write more about fisetin in order to justify this, but haven’t yet found the time. Here’s a single picture of a pretty mouse instead.

Name: Astaxanthin

Dosage: 12mg (included in BP)

Cost/day: $0.15

Information: Astaxanthin [Wikipedia, webmd, Examine] is a carotenoid generally derived from seafood. It’s suggested that it exhibits photoprotective, antioxidant, and anti-inflammatory effects, and has improved triglyceride and cholesterol levels as well as oxidative stress in humans, although not in completely healthy individuals.

Astaxanthin has increased the life span of C. elegans by 16-30%, with the authors stating “These results suggest that AX protects the cell organelle mitochondria and nucleus of the nematode, resulting in a lifespan extension via an Ins/IGF-1 signaling pathway during normal aging, at least in part”. While this is certainly interesting, expecting such a lifespan increase in humans is far too optimistic from this case alone.

However, Astaxanthin may be able to activate FOXO3 in humans, an important gene for human longevity which is present in many centenarians. Some other well-known natural compounds such as resveratrol and curcumin also interface with FoxOs, although these substances are still relatively speculative as far as anti-aging effects in humans go, even if they do have many strong supporters.

There’s some other interesting potential effects of astaxanthin, with some papers showing that it increases neural stem cell proliferation and may be useful to help curb dementia, and other papers showing that it can improve skin health and appearance, leading it to become an ingredient in some cosmetics.

Astaxanthin appears to be very safe in humans and is a relatively popular dietary supplement, with a market estimated at over $500M USD annually, although the majority of this supply is used as a component in animal feed and cosmetics.

Name: Curcumin

Dosage: 0-500mg (often discontinued, included in BP)

Cost/day: 0-$0.17 (varies)

Curcumin [Examine, webmd, Wikipedia] is a pigment found in tumeric. Curcumin’s strongest benefit seems to be the reduction in inflammation that it offers, although there appear to be some other areas that may be improved as well such as lipid profiles, mental health, potentially improved digestion, and reduced pain with some conditions such as osteoarthritis. It may exhibit a notable anti-tumor effect via apoptosis. It seems relatively safe, although has low bio-availability, so is often taken with substances to increases its availability such as piperine, or taken in an otherwise proprietary formulation that generally has some type of oil that improves bio-availability instead. As inflammation is important in aging and many other diseases, it’s something that is nice to be aware of.

I only sometimes take curcumin depending on my inflammation levels, generally measured via c-reactive protein.. When it is negligibly low, I stop taking it, and if I ever see it creep up in blood test results, I resume supplementation. Curcumin can be potentially tough on the liver, and in large doses has a greater potential to cause adverse affects. Some papers show quite a few potential drug interactions that can occur by taking curcumin, especially in larger doses, and via a variety of mechanisms, including its affect on platelets and potential interactions with enzymes such as CYP3A4, potentially affecting the metabolism of a large amount of drugs.

Name: Berberine

Dosage: 1.2g (discontinued, replaced with metformin which was then deprecated)

Cost/day: $0.28

Information: Berberine (Examine, webmd, Wikipedia] is an extract from various plants. It appears to be a pretty strong natural mimetic of metformin, a popular drug for diabetes with many alluring potential anti-aging properties. It often improves lipid profiles and blood glucose, and thus may have many of the long-term benefits that metformin may have. Concordantly, the possibility for digestive side-effects is relatively high, and it’s sometimes taken several times a day in smaller doses as a result. Examine suggestions that it also inhibits enzymes such as CYP2D6 to some extent, which could lead to undesirable interactions with some drugs. It’s likely better to be on metformin than berberine, as drugs are kept to a significantly higher regulatory standard than supplements are and we have much more data on users of metformin.

Name: Caffeine

Dosage: 50-200mg

Cost/day: $0.10 (much higher If drinks are considered)

Information: Caffeine [Examine, webmd, Wikipedia] is something you likely don’t need an introduction to. I try to keep my dosage relatively low to avoid issues with tolerance, using a combination of coffee, tea, or caffeine pills, depending on the amount desired and my mood. When taking 100mg or more of caffeine, I generally have 100mg of L-theanine as well.

Also worth noting you can buy caffeine mints or the nicer primary metabolite, paraxanthine

Name: L-theanine

Dosage: 0-200mg, (not taken often, 100mg if taken generally)

Cost/day: $0.20

Information: L-theanine [Examine, webmd, Wikipedia] is an amino acid that is present in tea leaves which is often combined with caffeine for supposedly synergistic effects on cognition and mood, improving the upsides of caffeine while helping to ameliorate some of the potential downsides. I generally only take it if I’m having more caffeine than average on a given day, since I keep my caffeine intake pretty low.

Name: Melatonin

Dosage: ~300mcg or less (not taken consistently)

Cost/day: $0.04

Information: Melatonin [Examine, webmd, Wikipedia, Gwern] is a hormone secreted by the pineal gland with an important role in regulating your sleep cycle. Melatonin production can be suppressed in many individuals that are otherwise healthy, for example by exposure to blue light from computer screens before bed (which solutions like the program f.lux and blue-light blocking glasses attempt to solve). The generally accepted benefits of melatonin are a reduction in the time to fall asleep, although some individuals claim that it reduces their need for sleep as well (often by 15-60 minutes). For those with sleep conditions such as insomnia or jet lag (or just being older in many cases), melatonin can be a much greater aid in improving sleep and quality of life.

One meta-analysis (K=10, N=653), found melatonin supplementation may have helped significantly reduce some instances of cancer mortality (R = 0.66 after 1yr). Some studies also find improvements in gastroprotection, healing and reducing the rate of stomach ulcers.

Melatonin has increased the lifespan of some mice by 18%, primarily given as a supplement later in life in an attempt to give older mice more effective pineal gland functionality (directly giving older mice the pineal glands of younger mice was also performed, which also was very beneficial). Melatonin levels similarly decline with age in humans (as most important things do), and supplementation may be increasingly beneficial as one ages.

The proper dose of melatonin to take varies between individuals and many melatonin pills for sale are dosed too high (5-10mg), so approximate self-experimentation can be used such as starting with 0.5mg and increasing your dosage until benefits are noticed. The above link to Gwern’s website on Melatonin points to a good in-depth analysis that is worth reading as well.

A few other things you may want to be aware of if you’re interested in melatonin is that you can buy delayed-release and extended-release versions easily otc. Additionally, you can use a beta-blocker like propanolol to inhibit melatonin synthesis to assist in circadian rhythm regulation.

Name: Spermidine

Dosage: ~1-10+mg (various sources, now included in BP, previous source was wheat germ)

Cost/day: ~$0.05

As of Jul 23 2020, I’ve added Spermidine to the list of what I take, currently taking it via wheat germ. Spermidine is a polyamine compound that can be found in aged cheese, soybeans, wheat germs, and human sperm. Supplementation of spermidine has extended lifespan across species, including in yeast, nematodes, flies, and mice. In humans, spermidine levels decline with aging. Spermidine can delay aging in humans, has notable cardioprotective capabilities, induces autophogy, improves healthspan, and more. Lots of wonderful results just searching for spermadine on pubmed.

Dosing for spermidine is difficult. It’s obviously very safe, but 1mg is likely not enough for the level of effect that we want. The average daily nutritional intake of spermidine varies from 7 to 25mg, and we can see how much one might want to consume for blood levels of spermidine to increase by 39%: perhaps 10mg per day (calculated by multiplying the 66g of natto consumed per day by its approximate spermidine content of 150mg/kg to yield 10mg per day). Although we don’t have plasma concentrations of spermine and spermidine in humans in relation to mortality, this is available in several mice studies. I need to spend more time on this, but I think one might want to supplement as much as 5-20mg of spermadine per day, assuming that it’s not present in their diet in notable quantities already (which is quite possible, as some Mediterranean, Japanese, and other diets contain notable quantities of it).

I currently consume spermidine via wheat germ, which seems to have around 243mg/kg of spermidine in it. If I wanted 10mg a day, this would result in having to consume 41g of wheat germ per day, which although feasible, is a bit tedious, potentially unsavory depending on the method of consumption, and would also result in an additional 164 calories consumed per day. There are some spermidine supplements on amazon, but I am not sure that I trust any of them very much (with the most recent one having the most obvious fake reviews I have ever seen on a supplement), and many of them are simply wheat germ inside of a capsule, which is not only likely to be an insufficient dosage, but also much more expensive. It may be worth mentioning for some readers that spermidine is also present in human sperm, but not in enough quantities to warrant consumption unless you consume copious amounts of it (~0.1mg per ejaculation, assuming 3.5mL and 31ug/Ml).

See also: collection of relevant spermidine study links and associated video from Mike Lustgarten

Name: Metformin

Dosage: 0.5-1g (discontinued for various reasons)

Cody/day: $0.16

Information: Metformin [webmd, Wikipedia] is a prescription drug for diabetes and is one of the most popular drugs taken by those interested in longevity, often taken for this purpose by individuals without diabetes. Metformin is said to mimic some of the potential benefits of caloric restriction. It increases the lifespan of mice, increasing AMPK activity and antioxidant protection, resulting in reductions in both oxidative damage accumulation and chronic inflammation. Lifespans of other organisms such as silkworms and nematodes are also increased. There exists a vast literature on Metformin with respect to its mechanisms of improving longevity apart from just this; it’s currently the most popular drug taken to combat aging.

Due to the prevalence of diabetes, Metformin has over 80 million users (the vast majority taking it for diabetes), which gives us wonderful data on its safety, with its side effects rarely including anything besides minor gastrointestinal issues. Metformin is also cheap, costing only $5-$25 a month in the United States. For the above reasons and many others, Metformin appears to be one of the best candidates for an anti-aging drug, leading it to become one of the only drugs making clinical progress in this area with trials such as TAME (Targeting Aging with Metformin). Metformin deserves a larger write-up than I’ve given it here, so you’re encouraged to perform your own research on it (just as you should for anything written about on this page).

For long-term Metformin usage, be sure that you are not hypoglycemic, as well as that your levels of vitamin B6 and B12 are in acceptable ranges, as deficiencies in these are slightly associated with Metformin usage. Metformin may also diminish some health improvements from exercise, and although more research is needed, this factor should be considered for non-diabetics considering Metformin usage. See also: Gwern on metformin

Name: Acarbose

Dosage: varies greatly, infrequently taken at the start of meals with high carbohydrates

Cost/day: $0-$1

Information: Acarbose is a simple diabetic drug which inhibits alpha glucosidase, causing your glucose to spike less than it normally would when ingesting carbohydrates. It is very safe and common, especially in countries such as the United States. Various studies on acarbose in mice have consistently shown it to expend lifespan, sometimes as high as 22% in males, generally much less in females. The probability this applies to humans is, in my opinion, moderately likely, although it is unlikely to be nearly as strong of an effect. Although mice have a lot of similarity with humans (more than many would expect!), their digestive system and diet are more dissimilar than most other categories. With that said, this drug is very safe and provably reduces the glucose spikes in your blood that occur when ingesting large amounts of carbohydrates, which in general seems to be a good thing. It therefore has a lot more potential when taken at the start of eating a large pizza rather than a normal meal (unless pizza is your normal meal, in which case it’s hard to blame you, but you should probably eat other things as well).

Name: 17-α-estradiol / estradiol valerate

Dosage: 0 mg / varies

Cost/day: $0-1

Description: 17-α-estradiol (a non-feminizing form of estrogen) significantly extends male mice lifespan, and this may apply to humans as well. This section turned long so I turned it into its own post. I currently micro-dose estrogen and am experimenting with some other potential solutions here myself; I’d like to write more on this and on related HPG interactions and estrogens/androgens in general. Past links included under this.

Male lifespan extension with 17‐α estradiol is linked to a sex‐specific metabolomic response modulated by gonadal hormones in mice https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6052402/Acarbose, 17-α-estradiol, and nordihydroguaiaretic acid extend mouse lifespan preferentially in males. https://www.ncbi.nlm.nih.gov/pubmed/242455

I’ve messed around with quite a few hormonal profiles but would like a lot more research in this area, especially on SERMs. If you have quality information in this area please message me!

Name: Taurine

Dosage: ~2g

Cost/day: $0.20

Information: Taurine [Wikipedia, Examine.com] is an amino acid plentiful in fish and meat. It gained popularity as a potential supplement for longevity when a study in 2023 showed it it to increase lifespan in mice by 10%+ with life expectancy at 28 months up 18-25% as well as a corresponding increase in healthspan. There are a lot of papers on taurine improving various categories of aging, far too many to even begin to list here. For a broad overview you can check out Effects and Mechanisms of Taurine as a Therapeutic Agent. Some suspect taurine may be one of the more prominent reasons why Mediterraneanesque diets and some Japanese populations have improved longevity. It seems to have notable GABAeric effects, with some reporting that it decreases or increases anxiety at higher doses.

Some foods that are plentiful in taurine include chicken (378mg/100g), tuna (332mg/100g), and slightly less but still large amounts in crab, shrimp, lamb, beef, eggs, and cheese. An equivalent dosage in humans for the longevity results found in mice may be somewhere in the range of 3-8g. This may seem like a large amount for a supplement, but if you were to eat 1lb of chicken that alone would contain ~1.7g. Acquiring notable amounts of taurine without supplementation can be difficult as a vegetarian and near-impossible as a vegan.

It’s also found in many energy drinks, sometimes in quantities as large as 0.5-1g, and there’s a bit of evidence that it may pair well to reduce the jittery aspect of caffeine in a way similar to l-theanine. It seems like 3g/day can be reasonably consumed safely, and I’d suspect that this carries at least up to 5=10g/day, if not much higher. I’m only moderately bullish (at most) on taurine improving human lifespan, especially if one begins with the assumption of a good diet, but I find it really interesting nonetheless.

Name: Semaglutide (now discontinued)

Dosage: 0.15-0.3mg (subcutaneous injection, once per week. may use in the future again)

Cost/day: $1-2 ($30-50/month, but reduced food intake can actually make this profitable to take!)

Description: Semaglutide [Wikipedia] is one of the most important inventions of the century. It is the weight loss drug known as Ozempic, Wegovy, or Rybelsus. There is so much literature on this drug (and it now has millions of prescriptions in the US) that I’m not going to go over it here, but the short version is that it not only works, but it works well, and seems to often have few or no negative side effects, and sometimes even positive side effects, from reduced cardiac events to many reports of improved willpower.

Obesity leads to millions of deaths, and now there is a cure for it which can actually be applied at-scale, even in the presence of relatively unrestrained markets with highly-addictive and caloric food. Semaglutide should receive a Nobel Prize.

Although it is known for being expensive when bought through FDA-approved mediums, it is possible to purchase it safely for significantly less as it is not a controlled substance. As I’m neither a doctor nor a lawyer, you should speak with your doctor if you’re interested in trying it out. If you have injectable (liquid) semaglutide, it should be refrigerated.

2024 update: I’ve discontinued semaglutide for two reasons, the first being that I no longer desire to lose more fat, and the second being that it reduces my hedonic baseline by a bit (that is, all of life is slightly less pleasurable). I may hop on it or try microdosing it in the future.

Name: Rapamycin

Dosage: 4-12mg (schedule and doses vary, taken at most once a week, many other factors)

Cody/day: $1-4

Information: Rapamycin is perhaps the most exciting substance for me in longevity right now. Rapamycin notably extends the lifespan of most organisms we have given it to thus far, but lacks proper research in humans aside from its use as an immunosuppressant. It’s a very popular drug to research in the area of longevity, and deserves a longer write-up than I’ve given it here. It’s also potentially quite dangerous and we have little data in humans (aside from those we give it to for organ transplants), so please don’t take it yourself (Jan 2021 update: mTOR Inhibitors Associated with Higher Cardiovascular Adverse Events ‐ A Large Population Database Analysis). Dosage for rapamycin is a bit tricky. There’s a lot of speculation involved, but it seems like many people converge onto something either like 6-8mg/week, or 8-15mg/2 weeks, perhaps with some breaks between.

2024 Update: Rapamycin blood tests are reasonably available – I currently shoot for around 25-45 ng/mL ~2 hours after initial ingestion as a reasonable baseline.

Out of all of the longevity agents I am interested in and/or take myself, it is likely to be the one that I have the highest hope for in humans. We have a decent understanding of the mechanism (compared to many other things, at least), it works very consistently and strongly in several other organisms, and the mechanism of action is strongly evolutionarily conserved. As for safety concerns, it seems like if taken in a low dosage and infrequently enough, the safety profile improves significantly and it may be a net-plus in many areas (this may be related to mtorc1 vs mtorc2 activation depending on the dosage and timing (it does have a pretty long half-life!), which also makes it seem like it can be taken without actually suppressing one’s immune system or causing some other undesirable effect categories).

Although I do know of many others that take rapamycin, I still don’t suggest it to anyone myself, firstly because I don’t offer medical advice of that nature regardless of my cost/benefit analysis (are there risks of potentially bad unknown side-effects with long-term usage? sure, but the risk of *not* taking longevity agents is also pretty large, and results in a much earlier likely death), and secondly because it is still likely to be higher risk than a lot of other simple things that I do often suggest to others, like glycine supplementation, which I see as close to zero risk. I’d hope that anyone that takes it themselves has blood panels done (if not much more) to ensure they’re not doing easily-observable harm to themselves as well. I’d like this section to be more comprehensive, but I’ll follow with some relevant pubmed papers for now:

Rapamycin and aging: When, for how long, and how much? https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4401992/

Rapamycin fed late in life extends lifespan in genetically heterogeneous mice https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2786175/

Rapamycin slows aging in mice. https://www.ncbi.nlm.nih.gov/pubmed/22587563

Rapamycin-mediated lifespan increase in mice is dose and sex dependent and metabolically distinct from dietary restriction https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4032600/

Mice Fed Rapamycin Have an Increase in Lifespan Associated with Major Changes in the Liver Transcriptome https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3883653/

Lifespan extension and cancer prevention in HER-2/neu transgenic mice treated with low intermittent doses of rapamycin https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4026081/

Longevity, aging and rapamycin https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4207939/

Rapamycin and other longevity-promoting compounds enhance the generation of mouse induced pluripotent stem cells. https://www.ncbi.nlm.nih.gov/pubmed/21615676

Dosing of rapamycin is critical to achieve an optimal antiangiogenic effect against cancer. https://www.ncbi.nlm.nih.gov/pubmed/15612989

Intermittent supplementation with rapamycin as a dietary restriction mimetic https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3249447/

Rapamycin increases lifespan and inhibits spontaneous tumorigenesis in inbred female mice. https://www.ncbi.nlm.nih.gov/pubmed/22107964

Towards natural mimetics of metformin and rapamycin. https://www.ncbi.nlm.nih.gov/pubmed/29165314

Name: Selegine (L-deprenyl)

Dosage: ~0-5mg/day

Cost/day: $0.25

Selegiline/L-deprenyl is a MAO-B (and sometimes MAO-A) inhibitor sometimes used to help treat Parkinson’s or depression which may be able to improve lifespan in humans.

Longevity study with low doses of selegiline/(-)-deprenyl and (2R)-1-(1-benzofuran-2-yl)-N-propylpentane-2-amine (BPAP). https://www.ncbi.nlm.nih.gov/pubmed/27777099

The significance of selegiline/(-)-deprenyl after 50 years in research and therapy (1965-2015). https://www.ncbi.nlm.nih.gov/pubmed/274804

Name: Epitalon

Dosage: 10mg/day for 5-10 days in a row, once or twice per year

Cost/day: $40

Epitalon is really interesting. A few concerns in humans and I don’t buy that the telomerase activation is the reason why it may have potential (if it does), but there’s a chance it passes EV calculations depending on how you do the math. I’ve tried it a few times and I’m uncertain if I’ll continue or not. More info here to be posted later.

Additional supplements I do not currently take

The above section concludes the actively-maintained list.

Under this I include a lot of links/notes from previous research, which is not comprehensive nor updated.

This section contains a list of supplements that I think might be worth taking, but that I currently don’t use. Substances in this section seem to be relatively safe, and I’m generally only not taking them because I have more doubts about their usefulness to me specifically.

Aspirin

Aspirin [Wikipedia] is used for more than just treating temporary pain or fevers. As an NSAID, it reduces both acute and long-term inflammation, and may also affect oxidant production, cytokine responses, and block glycooxidation reactions. Consuming a low dose of aspirin daily appears to lower the risk of CVD in higher-risk groups (generally older individuals with a relevant medical history), although appears to have little effect in otherwise healthy individuals. The risks of a few cancers may be lowered slightly by long-term continual use of aspirin, although this is generally a minor effect, and doesn’t seem to be the case for all types of cancer. Some organizations suggest daily aspirin use in small doses for those in certain risk groups, generally those that have already experienced a heart attack or stroke.

Among aspirin’s more common adverse effects is an increased risk of gastrointestinal bleeding, which is one of the reasons it’s not suggested by most organizations for otherwise healthy individuals with low CVD risk. Aspirin has increased the average lifespan (although not the maximum lifespan) of mice in some studies, but this is unlikely to be the case in humans unless significantly more needs to be taken, which would increase the probability of adverse effects notably.

To summarize, it’s very likely that continual aspirin usage reduces the risk of some types of cancer and moderately likely that it can reduce the risk of CVD in some higher-risk groups. Although side-effects are negligible for most individuals, it is difficult to tell if aspirin is worth taking for healthy and young individuals. It’s likely much more beneficial for the elderly or middle-aged, as they’re at a much higher risk of cancers as well as CVD. As a result of this, I don’t take aspirin regularly.

Cocoa Extract

Cocoa [Examine, webmd, Wikipedia] is well-known as a major component of chocolate. Although the sugar added to most modern chocolate definitely does not benefit one’s health, cocoa itself has many bioactive substances with potential benefits. Among the most notable is (-)-epicatechin, which can offer improvements in blood flow and a corresponding reduction in blood pressure for many individuals. As usual, the most notable improvements in blood pressure and cholesterol occurred in individuals with pre-existing elevated levels. Some age-related markers improve in mice when supplemented with (-)-epicatechin, although no direct increase in lifespan has yet been noted.

Supplementation with some form of cocoa (supplemented or consumed as ultra-dark chocolate) may be beneficial for some individuals, although consuming too much sugar with cocoa would likely offset any positive effects. Quality cocoa extract is more expensive than many of the other supplements listed on this page, coming in at $1-2 day for a proper dosage.

Also, I’d love to purchase this and test it on myself for awhile to see if the effects can easily be measured.

CoQ10

CoQ10 [Examine, webmd, Wikipedia] (Coenzyme Q10 / ubiquinone) is a substance found in meat and fish that is primarily present in mitochondria and aids ATP production. Although supplementation is likely safe, it’s difficult to find convincing evidence that CoQ10 supplementation would be effective for longevity. It may improve lipid peroxidation, blood flow and offer minor improvements in other areas, but in my opinion doesn’t appear to stand out from most supplements, both experimentally and theoretically.

Creatine

Creatine [Examine, webmd, Wikipedia] is an organic compound used in the recycling of ATP in humans. It can be found in notable amounts of muscle meat and can also be synthesized in humans via glycine, arginine, and methionine. Creatine is a very popular supplement for athletes with strong evidence that it notably increases power output and lean mass, with some evidence that it can offer minor improvements in related areas such as recovery, fatigue, and some biomarkers that are positively associated with quality anaerobic exercise. It’s very safe, has little potential for any side effects, and is relatively cheap. The only reason I don’t take creatine right now is that I’m not doing many activities to build muscle, although I’ll likely start taking it soon, even if only alongside basic resistance training, calisthenics, or even cardio.

Quercetin

Quercetin [Examine, webmd, Wikipedia] is a flavanoid found in fruits and vegetables. As usual, eating the right fruits and vegetables is good for you on its own, and may make supplementation less beneficial, or completely irrelevant. I likely get enough of this from my diet, although there may be benefits to infrequent high-dose supplementation.

L-carnitine

L-carnitine [Examine, webmd, Wikipedia] is an ammonium compound found in notable quantities in meat such as beef. Supplementation sometimes appears to offer some decent results, but I’ve determined that I like already get a sufficient amount from my diet.

PQQ

PQQ [Examine, Wikipedia] is a redox cofactor found in human breast milk and some foods such as kiwis. PQQ alters indicators of inflammation and mitochondrial-related metabolism. It’s likely very safe, the main reason I’m not currently taking it is there’s very little evidence showing that it notably benefits already-healthy young humans, and it costs a bit higher than most supplements on this page.

Resveratrol

Resveratrol [Examine, webmd, Wikipedia] cannot go without being mentioned, as the extract from grapes that inspired the ‘red wine is great for you’ craze many years ago, it has been a constant source of speculative benefits and is still a very popular supplement in longevity communities. Although it hasn’t quite lived up to its initial hype, there’s still a lot of research on how it may be beneficial for longevity in one way or another. I’m personally not very into resveratrol and don’t see it as that interesting by itself. A summary is currently excluded here and you’re encouraged to read the above links if interested, but to be rather blunt, I think resveratrol is very likely approximately worthless, and is just yet another case study in now media hype in no way correlates with actual efficacy.

Sulforaphane

Sulforaphane [Examine, webmd, Wikipedia] is a compound found in vegetables such as broccoli and cabbages, with the best sources of it being broccoli sprouts and cauliflower sprouts. I’ve taken sulforaphane previously, but it will be difficult to know if it had a notable effect on me or not. I’m currently focusing more on my diet and have decided against taking sulforaphane. I’ve excluded a research summary in favor of the above links.

Some other supplements I am currently considering

Nicotinamide Mononucleotide (NMN) (Wikipedia): todo

Nicottinamide Riboside (NR) (Wikipedia): todo

Pterostilbene (Wikipedia): todo

procyanidin (Wikipedia): todo, The flavonoid procyanidin C1 has senotherapeutic activity and increases lifespan in mice

Trimethylglycine

Trimethylglycine [Exmine, Wikipedia] is a betaine amino-acid derivative found in some plants. It is notable for reliably reducing homocysteine levels in healthy subjects, sometimes by as much as 10%, and as much as 10-40% in unhealthy individuals. It appears that it might have a slightly negative effect in increasing, or preventing to some extent a decrease in, LDL, which is why I’m currently not taking it. It’s a nice molecule to be aware of and might deserve a spot in my stack at a later point, but as usual it would be nice to have more research available.

A lot of supplements have been excluded from this list, including many which are very interesting. Individuals who follow nootropic or longevity communities will definitely be curious why their favorite substance may have been excluded from this page, to which my answer is mostly that there’s too many substances for me to include all of them, so I did quite a bit of picking personal favorites. Even so, there’s likely many substances I’d like to include, but which I haven’t yet heard about or done enough research on. Feel free to message me on Twitter if you have any great suggestions here.

More interesting and potentially unsafe substances

This section contains some brief notes and links on substances that appear to be a lot more ‘experimental’ than the above sections, but have some interesting potential. In some cases it’s impossible to find proper tests of safety, or even basic toxicity, in humans. Regardless, they’re all interesting chemicals, sometimes increasing the lifespan of organisms such as mice by large amounts. A lot of compounds have been excluded from this list as there are too many for me to list currently. The most interesting item of this list is currently rapamycin, by a large margin. Also see list of potential CRMs.

Allantoin

Allantoin is a compound present in some cosmetics, toothpaste, shampoo, lotions, and more, which has improved lifespan in C. elegans in multiple studies.

Lipid profiling of C. elegans strains administered pro-longevity drugs and drug combinations.
https://www.ncbi.nlm.nih.gov/pubmed/30351306

A network pharmacology approach reveals new candidate caloric restriction mimetics in C. elegans https://www.ncbi.nlm.nih.gov/pubmed/26676933

Alpha-ketoglutarate

α-Ketoglutaric acid (2-oxoglutaric acid) is one of two ketone derivatives of glutaric acid.

Alpha-Ketoglutarate: Physiological Functions and Applications: https://www.ncbi.nlm.nih.gov/labs/pmc/articles/PMC4703346/

Rejuvant®, a potential life-extending compound formulation with alpha-ketoglutarate and vitamins, conferred an average 8 year reduction in biological aging, after an average of 7 months of use, in the TruAge DNA methylation test: https://www.aging-us.com/article/203736/text

Astragalus Membranaceus

astragalus membranaceus contains a compound called TA-65 that may activate telomerase, extending the lengths of the shortest telomeres in humans. This compound is lacking in notable research, and much of what exists is clearly for-profit.

A natural product telomerase activator as part of a health maintenance program. https://www.ncbi.nlm.nih.gov/pubmed/20822369

Anti-Aging Implications of Astragalus Membranaceus (Huangqi): A Well-Known Chinese Tonic https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5758356/

Astragalus membranaceus: A Review of its Protection Against Inflammation and Gastrointestinal Cancers https://www.ncbi.nlm.nih.gov/pubmed/26916911

Rifampicin

Rifampicin is an antibiotic that has improved lifespan in C. elegans

Rifampicin reduces advanced glycation end products and activates DAF-16 to increase lifespan in Caenorhabditis elegans. https://www.ncbi.nlm.nih.gov/pubmed/25720500

Lipid profiling of C. elegans strains administered pro-longevity drugs and drug combinations.
https://www.ncbi.nlm.nih.gov/pubmed/30351306

C60 (buckminsterfullerene)

C60 is an interesting fullerene that has extended lifespan in some animals notable, but has little data on human consumption and safety. In an original study that gained quite a bit of attention, it was reported to ‘almost double’ the lifespan of rats. Now in 2021 the two most recent studies I see show that it did not extend lifespan, and that it only extended it by around 7%. There is less information on mechanism of action than we would want, but it is generally suggested to be related to free radicals.

There’s apparently quite a few people that have been taking this themselves, buying it from less-than-reputable Internet sources and hopefully not letting it be contaminated with light, as when exposed to light it degrades and becomes very dangerous to consume. This is certainly not something I plan to touch myself in with the current state of our knowledge on it, but it does seem like a very interesting chemical nonetheless.

Benzofuranylpropylaminopentane

Benzofuranylpropylaminopentane is an unusual and understudied drug, in some ways similar to selegiline noted above. It has prolonged lifespan to a minor extent, such as 4% in mice.

Longevity study with low doses of selegiline/(-)-deprenyl and (2R)-1-(1-benzofuran-2-yl)-N-propylpentane-2-amine (BPAP). https://www.ncbi.nlm.nih.gov/pubmed/27777099

nordihydroguaiaretic acid

nordihydroguaiaretic acid (NDGA) has extended the lifespan of mesquitos by 50%, and male mice by 10%.

Dietary nordihydroguaiaretic acid increases the life span of the mosquito. https://www.ncbi.nlm.nih.gov/pubmed/3749035

Acarbose, 17-α-estradiol, and nordihydroguaiaretic acid extend mouse lifespan preferentially in males. https://www.ncbi.nlm.nih.gov/pubmed/24245565

GDF11

GDF11 is also really interesting. Similar to Epitalon it’s obvious that the wikipedia article was authored by someone into longevity, but this is another thing I’m going to keep an eye on.

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