Influence of physical activity on the epigenetic clock: evidence from a Japanese cross-sectional study.

IF 4.8 2区 医学 Q1 GENETICS & HEREDITY
Masatoshi Nagata, Shohei Komaki, Yuichiro Nishida, Hideki Ohmomo, Megumi Hara, Keitaro Tanaka, Atsushi Shimizu
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Abstract

Background: Biological age, especially epigenetic age derived from the epigenetic clock, is a significant measure of aging, considering the differences in aging rates among individuals. The epigenetic clock, a machine learning-based algorithm, uses DNA methylation states to estimate biological age. Previous studies have reported inconsistent associations between physical activity (PA) and the epigenetic clock, especially second-generation clocks such as PhenoAge and GrimAge. This study aimed to clarify this relationship using cross-sectional data from Japanese participants aged 40-69.

Methods: We used two datasets from the Saga J-MICC study, of which 867 samples were available for analysis. DNA methylation data from peripheral blood samples were used to calculate the epigenetic age using the epigenetic clocks PhenoAge and GrimAge. PA and sedentary time were measured using a single-axis accelerometer, while self-reported PA, sedentary time, and covariates were assessed using a self-administered questionnaire. The association between PA or sedentary time and epigenetic age acceleration was assessed using multiple linear regression.

Results: Pearson's correlation coefficients between accelerometer-based and self-reported PA variables ranged from 0.09 to 0.20. Multivariable regression analysis showed that accelerometer-based PA and sedentary time were associated with epigenetic age decelerations and accelerations, respectively. However, self-reported PA was not associated with the epigenetic age accelerations.

Conclusions: These results indicate that reducing sedentary time and increasing PA were associated with slowing both PhenoAge and GrimAge, even in East Asian populations with different exercise habits, body shapes, and lifestyles. This study highlights the potential of objective second-generation epigenetic age acceleration as an outcome index for healthcare interventions and clinical applications.

体育锻炼对表观遗传时钟的影响:来自日本横断面研究的证据。
背景:考虑到个体之间衰老速度的差异,生物年龄,尤其是由表观遗传时钟得出的表观遗传年龄,是衡量衰老的一个重要指标。表观遗传时钟是一种基于机器学习的算法,它利用 DNA 甲基化状态来估算生物年龄。之前的研究报告称,体育锻炼(PA)与表观遗传时钟,尤其是第二代时钟(如 PhenoAge 和 GrimAge)之间的关系并不一致。本研究旨在利用日本 40-69 岁参与者的横断面数据澄清这种关系:我们使用了佐贺 J-MICC 研究的两个数据集,其中 867 个样本可供分析。外周血样本中的 DNA 甲基化数据被用来使用表观遗传时钟 PhenoAge 和 GrimAge 计算表观遗传年龄。活动量和久坐时间是通过单轴加速度计测量的,而自我报告的活动量、久坐时间和协变量则是通过自填问卷评估的。采用多元线性回归评估了运动量或久坐时间与表观遗传年龄加速度之间的关系:结果:基于加速度计的 PA 变量与自我报告的 PA 变量之间的皮尔逊相关系数介于 0.09 与 0.20 之间。多变量回归分析表明,加速度计PA和久坐时间分别与表观遗传年龄减速和加速有关。然而,自我报告的活动量与表观遗传年龄加速无关:这些结果表明,即使在运动习惯、体型和生活方式不同的东亚人群中,减少久坐时间和增加活动量也与减缓表观年龄和严峻年龄有关。这项研究强调了客观的第二代表观遗传年龄加速度作为医疗保健干预和临床应用结果指标的潜力。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
自引率
5.30%
发文量
150
期刊介绍: Clinical Epigenetics, the official journal of the Clinical Epigenetics Society, is an open access, peer-reviewed journal that encompasses all aspects of epigenetic principles and mechanisms in relation to human disease, diagnosis and therapy. Clinical trials and research in disease model organisms are particularly welcome.
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