Modified aging of elite athletes revealed by analysis of epigenetic age markers

Aging (Albany NY). 2018 Feb 15;10(2):241-252. doi: 10.18632/aging.101385.

Abstract

Recent progress in epigenomics has led to the development of prediction systems that enable accurate age estimation from DNA methylation data. Our objective was to track responses to intense physical exercise of individual age-correlated DNA methylation markers and to infer their potential impact on the aging processes. The study showed accelerated DNA hypermethylation for two CpG sites in TRIM59 and KLF14. Both markers predicted the investigated elite athletes to be several years older than controls and this effect was more substantial in subjects involved in power sports. Accordingly, the complete 5-CpG model revealed age acceleration of elite athletes (P=1.503x10-7) and the result was more significant amongst power athletes (P=1.051x10-9). The modified methylation of TRIM59 and KLF14 in top athletes may be accounted for by the biological roles played by these genes. Their known anti-tumour and anti-inflammatory activities suggests that intense physical training has a complex influence on aging and potentially launches signalling networks that contribute to the observed lower risk of elite athletes to develop cardiovascular disease and cancer.

Keywords: DNA methylation; KLF14; TRIM59; aging; elite athletes; epigenetic age; intense physical exercise.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Aging / blood
  • Aging / genetics*
  • Athletes
  • Case-Control Studies
  • DNA Methylation / genetics*
  • Epigenomics
  • Exercise / physiology*
  • Female
  • Genetic Markers
  • Humans
  • Intracellular Signaling Peptides and Proteins
  • Kruppel-Like Transcription Factors
  • Male
  • Membrane Proteins / metabolism*
  • Metalloproteins / metabolism*
  • Sp Transcription Factors / metabolism*
  • Tripartite Motif Proteins
  • Young Adult

Substances

  • Genetic Markers
  • Intracellular Signaling Peptides and Proteins
  • KLF14 protein, human
  • Kruppel-Like Transcription Factors
  • Membrane Proteins
  • Metalloproteins
  • Sp Transcription Factors
  • TRIM59 protein, human
  • Tripartite Motif Proteins