Marioni Riccardo E, Shah Sonia, McRae Allan F, Chen Brian H, Colicino Elena, Harris Sarah E, Gibson Jude, Henders Anjali K, Redmond Paul, Cox Simon R, Pattie Alison, Corley Janie, Murphy Lee, Martin Nicholas G, Montgomery Grant W, Feinberg Andrew P, Fallin M Daniele, Multhaup Michael L, Jaffe Andrew E, Joehanes Roby, Schwartz Joel, Just Allan C, Lunetta Kathryn L, Murabito Joanne M, Starr John M, Horvath Steve, Baccarelli Andrea A, Levy Daniel, Visscher Peter M, Wray Naomi R, Deary Ian J
Centre for Cognitive Ageing and Cognitive Epidemiology, University of Edinburgh, 7 George Square, Edinburgh, EH8 9JZ, UK.
Medical Genetics Section, Centre for Genomic and Experimental Medicine, Institute of Genetics and Molecular Medicine, University of Edinburgh, Edinburgh, EH4 2XU, UK.
Genome Biol. 2015 Jan 30;16(1):25. doi: 10.1186/s13059-015-0584-6.
DNA methylation levels change with age. Recent studies have identified biomarkers of chronological age based on DNA methylation levels. It is not yet known whether DNA methylation age captures aspects of biological age.
Here we test whether differences between people's chronological ages and estimated ages, DNA methylation age, predict all-cause mortality in later life. The difference between DNA methylation age and chronological age (Δage) was calculated in four longitudinal cohorts of older people. Meta-analysis of proportional hazards models from the four cohorts was used to determine the association between Δage and mortality. A 5-year higher Δage is associated with a 21% higher mortality risk, adjusting for age and sex. After further adjustments for childhood IQ, education, social class, hypertension, diabetes, cardiovascular disease, and APOE e4 status, there is a 16% increased mortality risk for those with a 5-year higher Δage. A pedigree-based heritability analysis of Δage was conducted in a separate cohort. The heritability of Δage was 0.43.
DNA methylation-derived measures of accelerated aging are heritable traits that predict mortality independently of health status, lifestyle factors, and known genetic factors.
DNA甲基化水平随年龄变化。近期研究已基于DNA甲基化水平确定了实足年龄的生物标志物。目前尚不清楚DNA甲基化年龄是否反映了生物年龄的各个方面。
在此,我们测试了人们的实足年龄与估计年龄(DNA甲基化年龄)之间的差异是否能预测晚年的全因死亡率。在四个老年纵向队列中计算了DNA甲基化年龄与实足年龄之间的差异(Δ年龄)。对来自这四个队列的比例风险模型进行荟萃分析,以确定Δ年龄与死亡率之间的关联。在调整年龄和性别后,Δ年龄每高出5岁,死亡风险就高出21%。在进一步调整童年智商、教育程度、社会阶层、高血压、糖尿病、心血管疾病和APOE e4状态后,Δ年龄每高出5岁的人群,死亡风险增加16%。在一个单独的队列中对Δ年龄进行了基于家系的遗传力分析。Δ年龄的遗传力为0.43。
DNA甲基化衍生的加速衰老指标是可遗传的特征,可独立于健康状况、生活方式因素和已知遗传因素预测死亡率。