Simpkin Andrew J, Cooper Rachel, Howe Laura D, Relton Caroline L, Davey Smith George, Teschendorff Andrew, Widschwendter Martin, Wong Andrew, Kuh Diana, Hardy Rebecca
MRC Integrative Epidemiology Unit at the University of Bristol, Population Health Sciences, Bristol Medical School, University of Bristol, Bristol, UK.
Insight Centre for Data Analytics, National University of Ireland, Galway, Galway, Ireland.
BMJ Open. 2017 Nov 1;7(10):e016708. doi: 10.1136/bmjopen-2017-016708.
Our aim was to investigate the association of epigenetic age and physical capability in later life. Having a higher epigenetic than chronological age (known as age acceleration (AA)) has been found to be associated with an increased rate of mortality. Similarly, physical capability has been proposed as a marker of ageing due to its consistent associations with mortality.
The MRC National Survey of Health and Development (NSHD) cohort study.
We used data from 790 women from the NSHD who had DNA methylation data available.
Epigenetic age was calculated using buccal cell (n=790) and matched blood tissue (n=152) from 790 female NSHD participants. We investigated the association of AA at age 53 with changes in physical capability in women from ages 53 to 60-64. Regression models of change in each measure of physical capability on AA were conducted. Secondary analysis focused on the relationship between AA and smoking, alcohol, body mass index (BMI) and socioeconomic position.
Three objective measures of physical capability were used: grip strength, standing balance time and chair rise speed.
Epigenetic age was lower than chronological age (mean 53.4) for both blood (50.3) and buccal cells (42.8). AA from blood was associated with a greater decrease in grip strength from ages 53 to 60-64 (0.42 kg decrease per year of AA, 95% CI 0.03, 0.82 kg; p=0.03, n=152), but no associations were observed with standing balance time or chair rise speed. Current smoking and lower BMI were associated with lower epigenetic age from buccal cells.
We found evidence that AA in blood is associated with a greater decrease in grip strength in British females aged between 53 and 60-64, but no association with standing balance time or chair rise speed was found.
我们的目标是研究晚年表观遗传年龄与身体能力之间的关联。已发现表观遗传年龄高于实际年龄(即年龄加速(AA))与死亡率增加有关。同样,由于身体能力与死亡率始终相关,它已被提议作为衰老的一个标志。
医学研究委员会全国健康与发展调查(NSHD)队列研究。
我们使用了来自NSHD的790名有DNA甲基化数据的女性的数据。
使用790名NSHD女性参与者的颊细胞(n = 790)和匹配的血液组织(n = 152)计算表观遗传年龄。我们研究了53岁时的年龄加速与53至60 - 64岁女性身体能力变化之间的关联。对身体能力各指标变化与年龄加速的回归模型进行了分析。二次分析重点关注年龄加速与吸烟、饮酒、体重指数(BMI)和社会经济地位之间的关系。
使用了三项身体能力的客观指标:握力、站立平衡时间和从椅子上起身的速度。
血液(50.3)和颊细胞(42.8)的表观遗传年龄均低于实际年龄(平均53.4)。53至60 - 64岁期间,血液中的年龄加速与握力下降幅度更大有关(年龄加速每增加一岁,握力下降0.42千克,95%可信区间为0.03至0.82千克;p = 0.03,n = 152),但与站立平衡时间或从椅子上起身的速度没有关联。当前吸烟和较低的BMI与颊细胞较低的表观遗传年龄有关。
我们发现有证据表明,血液中的年龄加速与53至60 - 64岁英国女性握力下降幅度更大有关,但与站立平衡时间或从椅子上起身的速度没有关联。