Common genetic variation affected epigenetic age estimates in these African cohorts, and a -aware predictor reduced ancestry-related error.
Evidence
This methylation-genotype analysis studied 138 people from Baka, ‡Khomani San, and Himba cohorts while benchmarking published predictors and developing a meQTL-minimized model.
Caveat
The cohorts were small and limited to three populations, so links between variants, lower epigenetic age acceleration, healthspan, and longevity remain inferential.
Simplified
Aging is associated with genome-wide changes in DNA methylation in humans, facilitating the development of epigenetic age prediction models. However, these models have been trained primarily on European-ancestry individuals and none account for the impact of methylation quantitative trait loci (). To address these gaps, we analyze the relationships between age, genotype, and CpG methylation in 3 understudied populations: central African Baka (n = 35), southern African ‡Khomani San (n = 52), and southern African Himba (n = 51). We show that published prediction methods yield higher mean errors in these cohorts compared to European-ancestry individuals and find that unaccounted-for DNA sequence variation may be a significant factor underlying this loss of accuracy. We leverage information about the associations between DNA genotype and CpG methylation to develop an age predictor that is minimally influenced by meQTL and show that this model remains accurate across a broad range of genetic backgrounds. Intriguingly, we also find that the older individuals and those with lower epigenetic age acceleration carry more genetic variants linked to reduced epigenetic age. These findings support the hypothesis that multiple heritable factors collectively influence healthspan and longevity in human populations.
Key numbers
4.62 years
Mean Error for Heritable Predictors
Mean absolute prediction error for heritable predictors in African test samples.
4.25 years
Mean Error for Non-Heritable Predictors
Mean absolute prediction error for non-heritable predictors in African test samples.
3211
Significant Age Associations Identified
Total significant age associations identified across 355,103 .
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