Key result
Ultra-marathon running linked to ~16 years younger biological age via longer leukocyte telomeres.
Cross-Sectional (n=123)
Telomere length is recognized as a marker of biological age, and shorter mean leukocyte telomere length is associated with increased risk of cardiovascular disease. It is unclear whether repeated exposure to ultra-endurance aerobic exercise is beneficial or detrimental in the long-term and whether it attenuates biological aging. We quantified 67 ultra-marathon runners' and 56 apparently healthy males' leukocyte telomere length (T/S ratio) using real-time quantitative PCR. The ultra-marathon runners had 11% longer telomeres (T/S ratio) than controls (ultra-marathon runners: T/S ratio = 3.5±0.68, controls: T/S ratio = 3.1±0.41; β = 0.40, SE = 0.10, P = 1.4×10(-4)) in age-adjusted analysis. The difference remained statistically significant after adjustment for cardiovascular risk factors (P = 2.2×10(-4)). The magnitude of this association translates into 16.2±0.26 years difference in biological age and approximately 324-648bp difference in leukocyte telomere length between ultra-marathon runners and healthy controls. Neither traditional cardiovascular risk factors nor markers of inflammation/adhesion molecules explained the difference in leukocyte telomere length between ultra-marathon runners and controls. Taken together these data suggest that regular engagement in ultra-endurance aerobic exercise attenuates cellular aging.
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Denham et al. (2013) conducted a cross-sectional in Healthy individuals (n=123). Ultra-endurance aerobic exercise vs. Apparently healthy males was evaluated on Leukocyte telomere length (T/S ratio) (β = 0.40, p=1.4×10(-4)). Ultra-marathon runners had significantly longer leukocyte telomeres than healthy controls (mean T/S ratio 3.5 vs 3.1; P=1.4x10^-4), translating to a 16.2 year difference in biological age.
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