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RESEARCH PAPER / 2026-01-18

Epigenetic insights of Olympic champions: nuclear and mitochondrial DNA methylation and regulators of aging.

Timea Teglas, Ferenc Torma, Zoltan Bori, Dora Aczel, Gergely Babszky, Takuji Kawamura, Mitsuru Higuchi, Gu Yaodong, Muhammad Lee, Steve Horvath, Zsolt Radak

Research Center for Molecular Exercise Science, Hungarian University of Sports Science, Alkotás U. 42-48, 1123, Budapest, Hungary.Research Center for Molecular Exercise Science, Hungarian University of Sports Science, Alkotás U. 42-48, 1123, Budapest, Hungary. · pubmed

Abstract

The interaction between nuclear (nDNA) and mitochondrial DNA (mtDNA) methylation is not well known in the healthy population. The D-loop methylation level of the Olympic champions (N = 58) was significantly lower than that of non-champions (N = 32) (~ 36% unadjusted mean difference p = 0.016, sex and age adjusted p = 0.017). Interestingly, the robust linear analysis revealed that biological sex is a significant factor in mtDNA D-loop methylation (estimate = 1.521, p = 0.033). On the other hand, we cannot find relationships between the methylation levels of mtDNA and nuclear DNA, suggesting distinct regulation of the methylation/demethylation process of mtDNA and nuclear DNA. DNA methylation-based aging clocks showed a significant relationship with the levels of Klotho, irisin, and its receptor (irisin receptor integrin alpha-V), as well as with epigenetic regulators such as ten-eleven translocation enzyme 2, which were measured using enzyme-linked immunosorbent assay. Therefore, the data suggest a complex regulatory process of epigenetic aging and raise the possibility that D-loop methylation may have functional relevance in health, which remains to be explored.

The following analysis is generated by AI and may contain errors. It is separate from the authors’ abstract and is not peer review.

Research summary

The paper suggests that lower D-loop methylation levels in Olympic champions may have functional relevance in health and aging. The study explores the interaction of DNA methylation with aging, which is directly related to understanding the biological mechanisms of longevity.

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