Zhao Xiang, Shi Yinhui, Tang Mengling
Department of orthopaedics, the Second Affiliated Hospital, Zhejiang University School of Medicine, Hangzhou, 310000, China.
Zhejiang Key Laboratory of Motor System Disease Precision Research and Therapy, Jiefang Road 88#, Hangzhou, Zhejiang, 310009, P. R. of China.
Aging Clin Exp Res. 2025 Aug 29;37(1):263. doi: 10.1007/s40520-025-03176-4.
Physical activity may mitigate osteoporosis progression by modulating telomere shortening processes.
To explore the mediating role of telomere length (TL) in the relationship between physical activity and bone mineral density (BMD).
This study enrolled 2,394 participants aged 50 years and older from the U.S. National Health and Nutrition examination Surveys. TL was measured by quantitative polymerase chain reaction (qPCR) method (TeloMean) and DNA methylation data (HorvathTelo), and accelerated telomere attrition was assessed through residual-based indices of TeloMeanAccel and HorvathTeloAccel. Physical activity was assessed via questionnaire and BMD was measured at multiple body sites. Multiple linear regression models were utilized to evaluate associations between TL metrics, physical activity, and BMD. Mediation analysis, restrict cubic spline (RCS) modeling, subgroup analyses and sensitivity analyses were further conducted.
After adjusting for covariates, TL metrics of TeloMean and HorvathTelo were found significantly positive correlations with BMD. HorvathTeloAccel, reflecting accelerated telomere shortening, also exhibited significant association with BMD. Physical activity demonstrated a significant positive association with total BMD (β = 0.046, 95%CI: 0.004-0.088). Mediation analysis revealed that TeloMean and HorvathTelo accounted for 4.78% and 20.86% of the total effect of physical activity on BMD, respectively, while HorvathTeloAccel explained 5.24% of the observed association.
Reduced physical activity and accelerated telomere attrition were related with BMD decline, and TL partially mediated the association. These findings suggest that enhancing physical activity could mitigate telomere shortening and promote bone health.
身体活动可能通过调节端粒缩短过程来减缓骨质疏松症的进展。
探讨端粒长度(TL)在身体活动与骨密度(BMD)关系中的中介作用。
本研究纳入了来自美国国家健康与营养检查调查的2394名50岁及以上的参与者。通过定量聚合酶链反应(qPCR)方法(TeloMean)和DNA甲基化数据(HorvathTelo)测量TL,并通过基于残差的TeloMeanAccel和HorvathTeloAccel指标评估加速的端粒损耗。通过问卷评估身体活动,并在多个身体部位测量BMD。使用多元线性回归模型评估TL指标、身体活动和BMD之间的关联。进一步进行中介分析、限制立方样条(RCS)建模、亚组分析和敏感性分析。
在调整协变量后,发现TeloMean和HorvathTelo的TL指标与BMD呈显著正相关。反映加速端粒缩短的HorvathTeloAccel也与BMD呈显著关联。身体活动与总BMD呈显著正相关(β = 0.046,95%CI:0.004 - 0.088)。中介分析显示,TeloMean和HorvathTelo分别占身体活动对BMD总效应的4.78%和20.86%,而HorvathTeloAccel解释了观察到的关联的5.24%。
身体活动减少和端粒损耗加速与BMD下降有关,且TL部分介导了这种关联。这些发现表明,增加身体活动可以减轻端粒缩短并促进骨骼健康。