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老年人长期心理社会压力的全表观基因组关联研究。

Epigenome-wide association study of long-term psychosocial stress in older adults.

作者信息

Opsasnick Lauren A, Zhao Wei, Schmitz Lauren L, Ratliff Scott M, Faul Jessica D, Zhou Xiang, Needham Belinda L, Smith Jennifer A

机构信息

Department of Epidemiology, School of Public Health, University of Michigan, Ann Arbor, MI, USA.

Survey Research Center, Institute for Social Research, University of Michigan, Ann Arbor, MI, USA.

出版信息

Epigenetics. 2024 Dec;19(1):2323907. doi: 10.1080/15592294.2024.2323907. Epub 2024 Mar 3.

Abstract

Long-term psychosocial stress is strongly associated with negative physical and mental health outcomes, as well as adverse health behaviours; however, little is known about the role that stress plays on the epigenome. One proposed mechanism by which stress affects DNA methylation is through health behaviours. We conducted an epigenome-wide association study (EWAS) of cumulative psychosocial stress ( = 2,689) from the Health and Retirement Study (mean age = 70.4 years), assessing DNA methylation (Illumina Infinium HumanMethylationEPIC Beadchip) at 789,656 CpG sites. For identified CpG sites, we conducted a formal mediation analysis to examine whether smoking, alcohol use, physical activity, and body mass index (BMI) mediate the relationship between stress and DNA methylation. Nine CpG sites were associated with psychosocial stress (all  < 9E-07; FDR q < 0.10). Additionally, health behaviours and/or BMI mediated 9.4% to 21.8% of the relationship between stress and methylation at eight of the nine CpGs. Several of the identified CpGs were in or near genes associated with cardiometabolic traits, psychosocial disorders, inflammation, and smoking. These findings support our hypothesis that psychosocial stress is associated with DNA methylation across the epigenome. Furthermore, specific health behaviours mediate only a modest percentage of this relationship, providing evidence that other mechanisms may link stress and DNA methylation.

摘要

长期的心理社会压力与负面的身心健康结果以及不良健康行为密切相关;然而,压力在表观基因组中所起的作用却鲜为人知。一种压力影响DNA甲基化的推测机制是通过健康行为。我们对来自健康与退休研究(平均年龄 = 70.4岁)的2689名参与者的累积心理社会压力进行了全表观基因组关联研究(EWAS),在789,656个CpG位点评估DNA甲基化(Illumina Infinium HumanMethylationEPIC Beadchip)。对于已识别的CpG位点,我们进行了正式的中介分析,以检验吸烟、饮酒、身体活动和体重指数(BMI)是否介导压力与DNA甲基化之间的关系。九个CpG位点与心理社会压力相关(所有P值 < 9E - 07;FDR q < 0.10)。此外,健康行为和/或BMI介导了九个CpG位点中八个位点压力与甲基化之间关系的9.4%至21.8%。一些已识别的CpG位点位于与心脏代谢特征、心理社会障碍、炎症和吸烟相关的基因内或附近。这些发现支持了我们的假设,即心理社会压力与全表观基因组的DNA甲基化相关。此外,特定的健康行为仅介导了这种关系的适度比例,这表明其他机制可能将压力与DNA甲基化联系起来。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/e46a/10913704/c1fb570c6b1f/KEPI_A_2323907_F0001_OC.jpg

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