Department of Epidemiology and Biostatistics, College of Public Health, Zhengzhou University, Zhengzhou 450001, China.
Guangzhou First People's Hospital, School of Medicine, South China University of Technology, Guangzhou 510006, China.
Nutrients. 2022 Aug 31;14(17):3597. doi: 10.3390/nu14173597.
To assess the associations of platelet traits and obesity indices with aging biomarkers (telomere length (TL) and mitochondrial DNA copy number (mtDNA-CN)).
A cross-sectional study was performed among 5091 rural Chinese adults. Obesity indices (waist circumference (WC), waist-to-hip ratio (WHR) and waist-to-height ratio (WHtR)) and platelet traits (plateletcrit (PCT), platelet large cell ratio (P-LCR), mean platelet volume (MPV) and platelet distribution width (PDW)) were collected by physical examination. The aging biomarkers were determined by quantitative real-time polymerase chain reaction. Generalized linear regression models and mediation analysis were applied to explore the relationships between platelet traits, obesity indices, and aging biomarkers.
The mean age of the participants was 56 years (range: 18-79). Each one-unit increment in WC, WHR and WHtR were related to a 0.316 (95% confidence interval (CI): -0.437, -0.196), 0.323 (95% CI: -0.513, -0.134) and 0.277 (95% CI: -0.400, -0.153) decrease in relative TL; or a 0.102 (95% CI: -0.197, -0.007), 0.109 (95% CI: -0.258, -0.041) and 0.101 (95% CI: -0.199, -0.004) decrease in relative mtDNA-CN. The proportions of obesity indices with aging biomarkers mediated by platelet indices ranged from 2.85% to 10.10%.
Increased central obesity indices in relation to shortened relative TL or decreased mtDNA-CN were mediated by platelet traits, indicating that obesity in association with the accelerated aging process may be partially attributable to abnormal platelet activity.
评估血小板特征和肥胖指数与衰老生物标志物(端粒长度(TL)和线粒体 DNA 拷贝数(mtDNA-CN))的相关性。
对 5091 名中国农村成年人进行横断面研究。通过体格检查收集肥胖指数(腰围(WC)、腰臀比(WHR)和腰高比(WHtR))和血小板特征(血小板压积(PCT)、血小板大细胞比(P-LCR)、平均血小板体积(MPV)和血小板分布宽度(PDW))。采用实时聚合酶链反应定量测定衰老生物标志物。应用广义线性回归模型和中介分析探讨血小板特征、肥胖指数与衰老生物标志物之间的关系。
参与者的平均年龄为 56 岁(范围:18-79 岁)。WC、WHR 和 WHtR 每增加一个单位,TL 相对值分别降低 0.316(95%置信区间(CI):-0.437,-0.196)、0.323(95% CI:-0.513,-0.134)和 0.277(95% CI:-0.400,-0.153);mtDNA-CN 相对值分别降低 0.102(95% CI:-0.197,-0.007)、0.109(95% CI:-0.258,-0.041)和 0.101(95% CI:-0.199,-0.004)。血小板指数与衰老生物标志物之间的肥胖指数比例范围为 2.85%至 10.10%。
与相对 TL 缩短或 mtDNA-CN 降低相关的中心性肥胖指数增加,与血小板特征有关,表明与衰老加速过程相关的肥胖可能部分归因于血小板活性异常。