Why the study?
Higher cardiorespiratory fitness is associated with reduced type 2 diabetes mellitus risk, but the underlying mechanisms remain incompletely understood.
Does higher cardiorespiratory fitness reduce incident type 2 diabetes risk in adults without baseline diabetes?
Does higher cardiorespiratory fitness reduce incident type 2 diabetes risk in adults without baseline diabetes?
Higher cardiorespiratory fitness is associated with a significantly lower risk of incident type 2 diabetes, a relationship partially mediated by biological aging.
Higher VO2max may reduce T2D risk partly via slower biological aging; hypothesis-generating and requires prospective confirmation before practice change.
Aims Higher cardiorespiratory fitness is associated with reduced type 2 diabetes mellitus ( T2D ) risk, but the underlying mechanisms remain incompletely understood. We investigated whether biological aging mediates the association between maximal oxygen uptake ( VO 2 max) and incident T2D risk. Materials and Methods This prospective cohort study included 54 418 UK Biobank participants aged 39–70 years without baseline diabetes. VO 2 max was estimated using a validated algorithm incorporating resting heart rate, physical activity, age, sex and body mass index. Biological age (BA) and phenotypic age (PhenoAge) were calculated from clinical biomarkers. Cox proportional hazards models estimated hazard ratios ( HRs ) and 95% confidence intervals ( CIs ), adjusting for sociodemographic, lifestyle and clinical factors. Linear regression analyses assessed cross‐sectional associations between VO 2 max and standardised glycaemic and lipid biomarkers. Mediation analysis quantified the proportion of association explained by biological aging measures. Results During 694 986 person‐years of follow‐up, 2628 participants developed T2D (incidence rate: 3.78 per 1000 person‐years). Compared to the lowest VO 2 max quartile, participants in the highest quartile had a 56% lower T2D risk ( HR 0.44, 95% CI = 0.39–0.50). Each standard deviation increase in VO 2 max was associated with a 28% lower risk ( HR 0.72, 95% CI = 0.68–0.76). BA acceleration mediated 8.2% (95% CI = 6.1%–10.8%) and PhenoAge acceleration mediated 9.1% (95% CI = 6.8%–12.1%) of the VO 2 max– T2D association. Protective associations were consistent across sex, age, ethnicity and genetic risk subgroups. VO 2 max showed strong inverse correlations with glucose ( β = −0.32), glycated haemoglobin ( β = −0.28), triglycerides ( β = −0.31) and a positive correlation with high‐density lipoprotein ( HDL) cholesterol ( β = 0.29). Conclusions Higher cardiorespiratory fitness demonstrates robust protective associations against T2D incidence, with biological aging mechanisms partially mediating this relationship.
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Liu et al. (2025) studied this question.
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