{"id":1124,"date":"2022-10-20T17:29:38","date_gmt":"2022-10-20T17:29:38","guid":{"rendered":"https:\/\/joshmitteldorf.peachpuff-wolverine-566518.hostingersite.com\/?p=1124"},"modified":"2022-10-20T22:18:01","modified_gmt":"2022-10-20T22:18:01","slug":"designing-a-methylation-clock-that-reliably-evaluates-anti-aging-interventions","status":"publish","type":"post","link":"https:\/\/scienceblog.com\/joshmitteldorf\/2022\/10\/20\/designing-a-methylation-clock-that-reliably-evaluates-anti-aging-interventions\/","title":{"rendered":"Designing a Methylation Clock that Reliably Evaluates Anti-aging Interventions"},"content":{"rendered":"

Can methylation clocks be relied on in this context? The earliest clocks<\/a> were trained on chronological age only, and yet they predicted morbidity and mortality better than chronological age. I’ve been enthusiastic about the technology since 2013. But recently there have been substantial challenges to the validity of all the existing clocks.\u00a0<\/span><\/em><\/p>\n

\n

An article published last week fulfills a wish I\u2019ve expressed in previous columns. I’ve believed that methylation clocks are the best tool that we have for evaluating anti-aging interventions, and there is potential to accelerate anti-aging trials enormously. But it\u2019s not proven that setting back any given methylation clock will result in added longevity.<\/span><\/p>\n

Methylation clocks are a surrogate for gene expression. The problem is that two things happen to gene expression with age.<\/span><\/p>\n

[1]<\/strong> Programmed aging turns on chronic inflammation and shuts down repair mechanisms with age.<\/span><\/p>\n

[2]<\/strong> The body is increasingly damaged, and repair mechanisms are triggered in response to that damage.<\/span><\/p>\n

Yes, the body is fighting with itself as we get older. Some of the epigenetic changes that happen are suicidal, but the fundamental self-protective responses are still in play.<\/span><\/p>\n

Suppose you take an anti-aging pill. If the pill makes you score younger according to [1] then you\u2019re destined to live longer; but if you score younger according to [2] the chances are your life will be further shortened.\u00a0<\/span><\/p>\n

The way most methylation clocks are derived gives you no indication what mix of [1] and [2] goes into the age algorithm. To complicate the situation further, a strong type [2] response might be an indication of more damage, which would be bad, or an effective hormetic response, which would be good.<\/span><\/p>\n

(I have argued that the PhenoAge<\/a> clock is probably biased toward [1], and I have worried that the GrimAge<\/a> clock may have a lot of [2].)<\/span><\/p>\n

This preprint by Ying et al<\/span><\/a>, a collaboration between the Gladyshev lab at Harvard and the Horvath lab at UCLA, uses bioinformatic methods to confront the problem head-on.\u00a0\u00a0<\/span><\/p>\n

\u201cIt is unclear whether the DNA methylation changes that are used to predict age are causal to aging-related phenotypes or are simply byproducts of the aging process that does not influence aging themselves.\u201d\u00a0<\/span><\/p><\/blockquote>\n

I would add: Or worse \u2014 some methylation changes with age actually mitigate damage [2], and \u201cresetting\u201d those would be damaging to health, probably shortening lifespan.<\/span><\/p>\n

The experiment we want to do would be to change methylation at thousands of CpGs in a sample of people and see how the change affects their health. This is way impractical, both because we cannot yet manipulate cytosine methylation directly, and because the number of subjects involved would be enormous. A practical approach would be to calibrate an aging clock against historic data using <\/span>remaining lifespan<\/i><\/b> as a target (see below, \u201cA Simpler Alternative\u201d). This procedure has not been followed, to my knowledge, but <\/span>PhenoAge<\/span><\/a>, <\/span>GrimAge<\/span><\/a>, and <\/span>Dunedin Pace<\/span><\/a> all have some features of this procedure.\u00a0<\/span><\/p>\n

The new article that I\u2019m reviewing here takes a different approach, deploying GWAS.<\/span><\/p>\n

GWAS<\/span><\/a> (Genome-Wide Association Studies) have been used in the past to correlate various health outcomes with common genetic variants. For example, one could look at 23-and-me data for people who have had heart attacks and compare to a matched sample of people who have not had heart attacks; then look for genome variations (SNPs) that tend to be different in the two groups. Fast computers can do millions of correlation calculations and report back the ones that show the strongest results.<\/span><\/p>\n

How might this be applied to methylation sites? Methylation affects which genes are turned on in an individual, rather than which allele of the gene that individual happens to have. The trick is to look for 3-way correlations. MeQTL stands for \u201cmethylation quantitative trait loci\u201d. There are SNPs that are associated both with methylation changes at particular CpGs and also with health outcomes. Maybe it is through the CpG that the methylation change is causing the health effect. How can they determine if this is the case? A proposal was put forward by Richardson et al [<\/span>2018<\/span><\/a>]<\/span><\/p>\n

Abstract<\/strong>
\nWe have undertaken a systematic Mendelian randomization (MR) study using methylation quantitative trait loci (meQTL) as\u00a0<\/span>genetic instruments to assess the relationship between genetic variation, DNA methylation and 139 complex traits. Using\u00a0<\/span>two-sample MR, we identified 1148 associations across 61 traits where genetic variants were associated with both proximal\u00a0<\/span>DNA methylation (i.e. cis-meQTL) and complex trait variation (P < 1.39 10<\/span>08<\/span>).<\/span> Joint likelihood mapping provided evidence\u00a0<\/b>that the genetic variant which influenced DNA methylation levels for 348 of these associations across 47 traits was also\u00a0<\/b>responsible for variation in complex traits.<\/b> These associations showed a high rate of replication in the BIOS QTL and\u00a0<\/span>UK Biobank datasets for 14 selected traits, as 101 of the attempted 128 associations survived multiple testing corrections\u00a0<\/span>(P < 3.91 10<\/span>04<\/span>). Integrating expression quantitative trait loci (eQTL) data suggested that genetic variants responsible for\u00a0<\/span>306 of the 348 refined meQTL associations also influence gene expression,<\/span> which indicates a coordinated system of effects\u00a0<\/b>that are consistent with causality. … <\/b>Though we are unable to distinguish mediation\u00a0<\/strong>from horizontal pleiotropy in these analyses<\/strong>, our findings should prove valuable in prioritizing candidate loci where DNA\u00a0<\/span>methylation may influence traits and help develop mechanistic insight into the aetiology of complex disease.\u00a0\u00a0<\/span>[<\/span>Richardson 2018<\/span><\/a>]\u00a0\u00a0<\/span><\/p><\/blockquote>\n

The method is to look for 3-way correlations between (A) the trait in question, (B) methylation of a particular CpG site and (C) a point genetic variation (SNP). It\u2019s a dangerous game for a number of reasons. First, scanning over a huge number of possibilities assures that some of them come up positive just by chance. If you run an experiment 20 times, you\u2019ll probably come up with some result (in one run) that shows up as statistically significant, with odds against chance of p<0.05. Similarly, if you search a million CpG sites to see if any of them are associated with your favorite trait, then one of them is bound to show up with an association so strong that you report p<10^<\/span>-6<\/span>. It sounds impressive to say p<0.000001, but in this case it\u2019s just the laws of chance operating on a huge number of possible associations.\u00a0<\/span><\/p>\n

The people who do these analyses are not incompetent. They know this, and they compensate by setting the threshold 100 times low, in this case p<10^<\/span>-8<\/span>. But these probabilities are always computed based on a number of unverifiable assumptions, and it\u2019s always possible that some chance association slips in.<\/span><\/p>\n

There\u2019s a second problem with these 3-way associations. Remember that what we\u2019re trying to establish is that a particular CpG causes a particular trait.<\/span><\/p>\n

CpG \u21d2 trait\u00a0<\/span><\/p>\n

\u00a0Lacking a way to directly correlate the CpG with the trait, this method relies on the fact that both the trait and the CpG are associated with the same SNP. The \u201ccausal\u201d implication is that<\/span><\/p>\n

SNP \u21d2 CpG \u21d2 trait\u00a0<\/span><\/p>\n

But the authors gloss over the possibility that<\/span><\/p>\n

SNP \u21d2 trait\u00a0 \u00a0 \u00a0and
\n<\/span>SNP \u21d2 CpG\u00a0<\/span><\/p>\n

In words: Suppose the SNP has two actions (pleiotropy is the rule rather than the exception) so that it independently causes the trait and the CpG methylation. In this case, there is no indication that the CpG actually causes the trait. An even worse possibility is this:<\/span><\/p>\n

SNP \u21d2 trait \u21d2 CpG<\/span><\/p>\n

This is particularly worrisome. For example if the trait is inflammation, you would like to establish the fact that this particular methylation site causes inflammation. But if the CpG is associated with a quenching response to inflammation, then you\u2019d expect that CpG activation might be part of the body’s solution to perceived inflammation.\u00a0<\/span><\/p>\n

The fact that you tend to see fire trucks and fires in the same places around a city doesn\u2019t mean that the fire trucks cause fires.\u00a0\u00a0<\/span><\/p>\n

I am all for using fancy statistics to learn about the metabolism. But the headier the statistics you use, the more you have to worry about things that could go wrong.<\/span><\/p>\n

This is all in the context of my limited sophistication with advanced statistical methods. The authors of this study recognize all the hazards that I have catalogued, and they present arguments why they have effectively compensated for them. I don\u2019t have the background to pass judgment on those arguments.\u00a0<\/span><\/p>\n

\u201cHere, we leveraged large-scale genetic data and performed epigenome-wide Mendelian Random<\/span> ization (EWMR) on 420,509 CpG sites to identify CpG sites that are causal to twelve aging-related<\/span>\u00a0 <\/span>traits. We found that none of the existing clocks are enriched for causal CpG sites.\u201d<\/span><\/p><\/blockquote>\n

I take this as a red flag. How can it be that there is negligible overlap between the CpGs found by this new GWAS methodology and any of the Horvath clocks of the past? I believe that aging is driven at a deep level by epigenetic changes, and this gives credibility to the idea behind methylation clocks. I have acknowledged the risk that these clocks may be polluted with some CpGs that are not drivers of aging [1] but responses to aging [2]. But if these new results are to believed, we have to throw out GrimAge and PhenoAge as worse than useless.\u00a0<\/span><\/p>\n

\u201cContradicting the popular notion that most age-related changes are bad for the organism, our findings revealed that, in terms of the number of CpGs, there was no enrichment for either protective or damaging methylation changes during aging.\u201d<\/span><\/p><\/blockquote>\n

The first two papers to propose that methylation is a primary driver of aging appeared in 2012 [one<\/a>, two<\/a>]. I was an enthusiastic supporter in 2013<\/a>. A decade later, these papers have seeded an entire field of study. But the above captioned statement suggests that this was all in vain, that methylation changes with age are a correlation only, and they don\u2019<\/span>t really have to do with either drivers of aging [1] or protection from damage [2].<\/p>\n

\u201cOur results suggest that the known lifespan-related effect [of APOE] may be mediated by DNA methylation.\u201d <\/span><\/p><\/blockquote>\n

This in itself is a stunning conclusion, and should lead to methylation-based therapies for the millions of people who are at elevated risk of AD and CVD based on APOE4 in their genomes.\u00a0<\/span><\/p>\n

Three new clocks<\/b><\/h2>\n

Ying et al announce the creation of three new methylation clocks based on the science described above. <\/span>CausAge<\/span><\/i> was developed using traditional methods with an additional boost for sites that are identified through GWAS as associated with causes of age-related decline. <\/span>DamAge<\/span><\/i> was designed to include only sites that are associated with increasing damage to the body; while <\/span>AdaptAge<\/span><\/i> was designed to be based on the opposite \u2014 sites associated with protective adaptations. Scoring older on the <\/span>DamAge<\/span><\/i> clock is presumably a bad thing because it indicates more damage, while scoring older on the <\/span>AdaptAge<\/span><\/i> clock should be associated, paradoxically, with a <\/span>longer<\/i><\/b> life expectancy. \u201cTherefore, we hypothesized that DamAge acceleration may be harmful and shorten life expectancy, whereas AdaptAge acceleration would be protective or neutral, which may indicate healthy longevity.\u201d I had to read this sentence several times because it was the reverse of what I expected from the text. Based on this sentence, I\u2019m guessing that <\/span>DamAge<\/span><\/i> corresponds to what I called [1] above, and <\/span>AdaptAge<\/span><\/i> is [2].\u00a0<\/span><\/p>\n

\u201cWe found that short-term treatment with cigarette smoke condensate in bronchial<\/span> epithelial cells significantly accelerated DamAge but did not affect other tested clocks (Fig. 6c). Additionally, a 6-week omega-3 fatty acid supplementation in overweight subjects, which has been shown to be protective against age-related cardiovascular diseases, significantly increased AdaptAge and reduced DamAge (Fig. 6c).\u201d<\/span><\/p><\/blockquote>\n

This is another question mark for me. Cigaratte smoke makes DamAge <\/em>look older. I have always imagined that the direct effect of smoke is to damage lung tissue, and that some kind of epigenetic response to this is the body\u2019<\/span>s attempt to protect itself. That would be a type [2] (hormetic) response. But according to the above captioned sentence, cigarette smoke has a direct and detrimental effect on methylation, a type [1] response. I can\u2019t say this is impossible, just unexpected.<\/span><\/p>\n

A Simpler Alternative<\/b><\/h2>\n

The ideal methylation clock would be rooted in a deep understanding of biochemistry. We would know which genes are associated with inflammation, with immune senescence, with sex hormones, with apoptosis, with blood lipids\u2014and also which CpGs turn these genes on and off. This kind of detail is not available at present, but it is a reasonable long-range goal.\u00a0<\/span><\/p>\n

Here\u2019s my proposal for creating an aging clock that measures what we are most interested in: is a given person\u2019s biological age older or younger than others of the same chronological age?<\/span><\/p>\n

Start with a historic sample of methylation profiles from biobanked samples of people who have died in the intervening years. Train a new methylation clock on the number of years that each subject survived since the sample was drawn, and include in the target a penalty for chronological age. In other words, the training target is the number of years the person actually lived minus the number of years he would have been expected to live given his chronological age.\u00a0<\/span><\/p>\n

(After juggling in my mind the gender of pronouns in the previous sentence, I realize that, given what we know about different aging mechanisms by sex, we really should do this analysis so as to create separate methylation clocks for men and women.)<\/span><\/p>\n

There is a lot more data available now than when Steve Horvath did his pioneering work in 2012-13. His clocks have been constrained to be linear in each methylation site for adults. But we have reason to believe that epigenetic changes <\/span>come in waves<\/span><\/a>, with different methylation sites being most important at different ages. So let\u2019s calibrate two different clocks for each decade of life, and for men and women.<\/span><\/p>\n

While I\u2019m making a wish list, I would add that my ideal methylation clock should avoid being too sensitive to any one CpG. This is for the practical reason that there are quality control issues that come from lab technique and from manufacture of bead chips.\u00a0<\/span><\/p>\n

The problem comes from having large positive and negative contributions in the age algorithm, which cancel sensitively in the final result. The way to avoid this problem is to derive two separate clocks, one based only on CpGs that increase methylation with age and the other based only on those that decrease methylation with age; then average the two calculations for the plus and minus clocks.\u00a0<\/span><\/p>\n

I believe this project is more than feasible, it should be a lot less work than the present analysis by Ying et al. And for me, it would have the advantage of being transparent, not dependent on unnecessary assumptions, and avoiding indirect references from 3-way correlations. If anyone reading this has access to the data, I would love to do the statistics.<\/span><\/p>\n

And why should we have faith that the construction I outline should lead predominantly to sites that have a causal relationship to senescence [1]? It\u2019s not a slam dunk, but the fact that a person dies later than expected is a good indication that protective\u00a0 responses are up and programmed aging is down. Our understanding of the situation is confounded by hormesis.\u00a0<\/span><\/p>\n

The Bottom Line<\/b><\/h2>\n

This new work should cause re-thinking of all the anti-aging work of the last several years that has relied on methylation clocks to gauge success. The message is that the clocks that have been developed so far are at best orthogonal to the real causes of aging, and at worst they could be encouraging interventions that actually shut off the body\u2019s natural protections. If we believe the new results, <\/span>DamAge<\/span><\/i> would be a far better choice than anything previously available for any anti-aging trial, but the difference <\/span>DamAge <\/span><\/i>minus<\/span> AdaptAge<\/span><\/i> might be even better.\"\"<\/span><\/p>\n

As the <\/span>DataBETA project<\/span><\/a> is launched this fall, I have a direct professional interest in choosing the right technology to evaluate a wide range of interventions and combinations that are commonly used by people who are trying to live longer.<\/span><\/p>\n

I have been enthusiastic about methylation clocks from the beginning on the basis that (A) for theoretical reasons, I find it credible that epigenetics drives aging, and (B) the original Horvath clock, derived only from chronological age, predicts mortality better than chronological age. I have a hard time throwing that reasoning out based on one new preprint. But there has also been <\/span>Katcher\u2019s lifespan experiment<\/span><\/a>, and <\/span>Levine\u2019s caution<\/span><\/a> based on theoretical grounds, both of which have shaken my faith in methylation clocks earlier this year.<\/span><\/p>\n

Frankly, if Horvath\u2019s name hadn\u2019t been on this ms, I would not have been inclined to take it seriously. Should we believe the new results, which seem to discredit all the analysis that he and others have done in the first decade of epigenetic clocks?<\/span><\/p>\n

I don\u2019t have the expertise to answer this question. I can hope that this work receives a deep and respectful challenge during the peer review process, and that people with more statistical chops than I have will debate both sides of this question over the coming months.\u00a0<\/span><\/p>\n","protected":false},"excerpt":{"rendered":"

Can methylation clocks be relied on in this context? The earliest clocks were trained on chronological age only, and yet they predicted morbidity and mortality better than chronological age. I’ve been enthusiastic about the technology since 2013. But recently there have been substantial challenges to the validity of all the existing clocks.\u00a0 An article published … Read more<\/a><\/p>\n","protected":false},"author":65,"featured_media":1125,"comment_status":"open","ping_status":"open","sticky":false,"template":"","format":"standard","meta":{"jetpack_post_was_ever_published":false,"_jetpack_newsletter_access":"","_jetpack_dont_email_post_to_subs":false,"_jetpack_newsletter_tier_id":0,"_jetpack_memberships_contains_paywalled_content":false,"_jetpack_memberships_contains_paid_content":false,"footnotes":""},"categories":[1],"tags":[],"class_list":["post-1124","post","type-post","status-publish","format-standard","has-post-thumbnail","hentry","category-uncategorized"],"yoast_head":"\nDesigning a Methylation Clock that Reliably Evaluates Anti-aging Interventions - Josh Mitteldorf<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/scienceblog.com\/joshmitteldorf\/2022\/10\/20\/designing-a-methylation-clock-that-reliably-evaluates-anti-aging-interventions\/\" \/>\n<meta property=\"og:locale\" content=\"en_US\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Designing a Methylation Clock that Reliably Evaluates Anti-aging Interventions\" \/>\n<meta property=\"og:description\" content=\"Can methylation clocks be relied on in this context? The earliest clocks were trained on chronological age only, and yet they predicted morbidity and mortality better than chronological age. I’ve been enthusiastic about the technology since 2013. But recently there have been substantial challenges to the validity of all the existing clocks.\u00a0 An article published ... 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