OBJECTIVE mtDNA copy number (CN) reflects mitochondrial function, but prior studies have reported inconsistent associations with type 2 diabetes risk, ranging from inverse to positive or null findings. We hypothesized that mtDNA-CN is nonlinearly associated with incident type 2 diabetes. RESEARCH DESIGN AND METHODS We included 34,835 adults without diabetes from the Kunshan Aging Research With E-Health (KARE) cohort and 289,338 from the UK Biobank (UKB). Associations between blood mtDNA-CN and incident type 2 diabetes were evaluated using Cox proportional hazards and restricted cubic spline models stratified by age. RESULTS A U-shaped association was observed in the KARE cohort (P 0.001), in which the hazard ratios (95% CIs) across increasing mtDNA-CN quartiles were 1.00 (reference), 0.94 (0.88–1.00), 0.85 (0.79–0.91), and 0.93 (0.87–1.00). In contrast, the UKB cohort exhibited a predominantly inverse linear trend. Age-stratified analyses revealed that this U-shaped association was particularly evident in younger participants (aged 65 years in KARE and 50 years in UKB), indicating elevated diabetes risk at both low and high mtDNA-CN levels. Additionally, mtDNA-CN declined with age in both cohorts, with an accelerated decrease beyond ∼65 years in KARE and ∼50 years in UKB. CONCLUSIONS Blood mtDNA-CN showed a U-shaped association with incident type 2 diabetes in younger individuals.
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Xiaoyin Huang
Z. F. Tian
Yi Pan
Diabetes Care
Peking University
Chinese Academy of Medical Sciences & Peking Union Medical College
Jiangsu University
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Huang et al. (Mon,) studied this question.
www.synapsesocial.com/papers/69ba427c4e9516ffd37a2c08 — DOI: https://doi.org/10.2337/dc25-2198
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