Journal Article
DNA methylation clock DNAmFitAge shows regular exercise is associated with slower aging and systemic adaptation
Matyas Jokai; Ferenc Torma; Kristen M. McGreevy; Erika Koltai; Zoltan Bori; Gergely Babszki; Peter Bakonyi; Zoltan Gombos; Bernadett Gyorgy; Dora Aczel; Laszlo Toth; Peter Osvath; Marcell Fridvalszky; Timea Teglas; Aniko Posa; Sylwester Kujach; Robert Olek; Takuji Kawamura; Yasuhiro Seki; Katsuhiko Suzuki; Kumpei Tanisawa; Sataro Goto; Csaba Kerepesi; Istvan Boldogh; Xueqing Ba; Kelvin J. A. Davies; Steve Horvath; Zsolt Radak
GeroScience · Vol. 45, Issue 5 · pp. 2805-2817 · 2023
Abstract
DNAmPhenoAge, DNAmGrimAge, and the newly developed DNAmFitAge are DNA methylation (DNAm)-based biomarkers that reflect the individual aging process. Here, we examine the relationship between physical fitness and DNAm-based biomarkers in adults aged 33–88 with a wide range of physical fitness (including athletes with long-term training history). Higher levels of VO 2 max ( ρ = 0.2, p = 6.4E − 4, r = 0.19, p = 1.2E − 3), Jumpmax ( p = 0.11, p = 5.5E − 2, r = 0.13, p = 2.8E − 2), Gripmax ( ρ = 0.17, p = 3.5E − 3, r = 0.16, p = 5.6E − 3), and HDL levels ( ρ = 0.18, p = 1.95E − 3, r = 0.19, p = 1.1E − 3) are associated with better verbal short-term memory. In addition, verbal short-term memory is associated with decelerated aging assessed with the new DNAm biomarker FitAgeAcceleration ( ρ : − 0.18, p = 0.0017). DNAmFitAge can distinguish high-fitness individuals from low/medium-fitness individuals better than existing DNAm biomarkers and estimates a younger biological age in the high-fit males and females (1.5 and 2.0 years younger, respectively). Our research shows that regular physical exercise contributes to observable physiological and methylation differences which are beneficial to the aging process. DNAmFitAge has now emerged as a new biological marker of quality of life.