表观遗传年龄和发生心房的风险
Jason D Roberts1,2, Eric Vittinghoff3, Ake T Lu4
1Population Health Research Institute (J.D.R., P.M-S., G.P.).
Circulation
|September 30, 2021
概括
表观遗传加快衰老 (EAA) 与心房风险增加有关,这表明生物衰老对心脏健康的影响与时间年龄无关. 这些衰老过程可能是可修改的,
科学领域:
- 遗传学
- 表观遗传学
- 心脏病学
背景情况:
- 年龄是心房的主要风险因素,但其潜在机制尚不清楚.
- 表观遗传修饰预测时间的年龄,并且偏差 (表观遗传年龄加速,EAA) 可能表明生物衰老加速.
研究的目的:
- 研究表观遗传年龄测量与心房的发生率之间的关联.
主要方法:
- 使用了3个基于人口的队列的数据,测量了4个表观遗传时钟 (Horvath,Hannum,DNAm PhenoAge,DNAm GrimAge) 和DNAm PAI-1.
- 使用考克斯模型和元分析来评估发生的AF风险,并对因果关系进行孟德尔随机分析.
主要成果:
- 经过对时间年龄和其他风险因素进行调整后,表观遗传年龄加速 (EAA) 测量,特别是DNAm GrimAge和DNAm PhenoAge,显著与发生性AF的风险增加有关.
- 在DNAm GrimAge和DNAm PhenoAge的5年EAA增加与分别19%和15%更高的AF发生率相关.
- 孟德尔随机分析没有确定统计学上显著的因果关系.
结论:
- 经过调整后,EAA与发生的AF之间的关联表明生物衰老与时间衰老无关.
- 确定的衰老过程可能是可修改的,为AF预防或干预提供了潜在的途径.
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