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积极和消极社会经历与表观遗传衰老之间的关联。

Associations between positive and negative social experiences and epigenetic aging.

作者信息

Prigerson Holly G, Russell David, Maciejewski Paul K

机构信息

Department of Radiology, Weill Cornell Medicine, 420 East 70Th Street, Lasdon House, Suite 4B, Room 423, New York City, NY, 10021, USA.

Cornell Center for Research on End-of-Life Care, New York City, NY, 10065, USA.

出版信息

Sci Rep. 2025 Jul 1;15(1):22284. doi: 10.1038/s41598-025-07222-z.

Abstract

Associations between positive and negative social experiences and epigenetic aging are not well understood. To determine associations between positive and negative social experiences and epigenetic aging. Data from Midlife in the United States (MIDUS), a US population-based longitudinal cohort study, were used to examine relationships between social experiences and epigenetic aging. Participant reports of social experiences were assessed at survey waves closest to the subsequent collection of blood samples for DNA methylation testing and epigenetic clock calculation from 2004 to 2009 (MIDUS Core Sample) or 2012-2016 (MIDUS Refresher Sample). Analyses were conducted May 2024-June 2025. Self-reported positive (e.g., marriage, attendance at social meetings) and negative (e.g., parent's drug problems, incarceration) social experiences were examined. Epigenetic was assessed from blood DNA methylation using the GrimAge and DunedinPACE epigenetic clocks. The sample (N = 1309) was 55.5% female, 22.5% Black and averaged 51.3 (SD = 12.5) years of age. In models adjusted for sociodemographic and health confounders, participants who reported positive social experiences such as being married (GrimAge: β = - 0.807, SE = 0.269, p < 0.01; Dunedin: β = - 0.022, SE = 0.007, p < 0.01) and engaging in social meetings (GrimAge β = - 1.027, SE = 0.250, p < 0.01; Dunedin: β = - 0.020, SE = 0.007, p < 0.01) exhibited significantly decelerated GrimAge scores; participants who reported negative social experiences such as a parent experiencing drug problems (GrimAge β = 2.430, SE = 0.761, p < 0.001), dropping out of school (GrimAge β = 2.869, SE = 0.405, p < 0.001; Dunedin β = 0.046, SE = 0.011, p < 0.001), and imprisonment (GrimAge β = 1.922, SE = 0.520, p < 0.001) exhibited significantly accelerated epigenetic aging scores. Adjusted models found the sum of positive social experiences was associated with decelerated epigenetic aging scores (GrimAge β = - 0.431, SE = 0.109, p < 0.001; Dunedin β = - 0.009, SE = 0.003, p < 0.01) and that the sum of negative social experiences was associated with accelerated epigenetic aging scores (GrimAge β = 0.934, SE = 0.162, p < 0.001; Dunedin β = 0.015, SE = 0.004, p < 0.01). Respondents with a "net positive" ratio of positive to negative social experiences had GrimAge scores that were 4.63 years younger on average than those with "net negative" social experiences (β = - 4.729; SE = 0.507; p < 0.001; adjusted β including covariates = - 2.847; SE = 0.469; p < 0.001). Associations of positive and negative social experiences with epigenetic aging were found to be independent of respondents' perceived social support and their self-rated physical and mental health. Results suggest that negative social experiences accelerate while positive social experiences decelerate epigenetic aging. Negative and positive social experiences are each independently associated with epigenetic aging and net positive social experiences are associated with slower epigenetic aging.

摘要

积极和消极社会经历与表观遗传衰老之间的关联尚未得到充分理解。为了确定积极和消极社会经历与表观遗传衰老之间的关联。来自美国中年(MIDUS)研究的数据,这是一项基于美国人群的纵向队列研究,被用于检验社会经历与表观遗传衰老之间的关系。在2004年至2009年(MIDUS核心样本)或2012 - 2016年(MIDUS更新样本)最接近随后采集血液样本进行DNA甲基化检测和表观遗传时钟计算的调查波次中,评估参与者的社会经历报告。分析于2024年5月至2025年6月进行。研究了自我报告的积极(如结婚、参加社交会议)和消极(如父母的药物问题、监禁)社会经历。使用GrimAge和达尼丁PACE表观遗传时钟从血液DNA甲基化评估表观遗传。样本(N = 1309)中女性占55.5%,黑人占22.5%,平均年龄为51.3岁(标准差 = 12.5)。在针对社会人口统计学和健康混杂因素进行调整的模型中,报告了诸如结婚(GrimAge:β = - 0.807,标准误 = 0.269,p < 0.01;达尼丁:β = - 0.022,标准误 = 0.007,p < 0.01)和参加社交会议(GrimAge β = - 1.027,标准误 = 0.250,p < 0.01;达尼丁:β = - 0.020,标准误 = 0.007,p < 0.01)等积极社会经历的参与者,其GrimAge得分显著减速;报告了诸如父母有药物问题(GrimAge β = 2.430,标准误 = 0.761,p < 0.001)、辍学(GrimAge β = 2.869,标准误 = 0.405,p < 0.001;达尼丁β = 0.046,标准误 = 0.011,p < 0.001)和监禁(GrimAge β = 1.922,标准误 = 0.520,p < 0.001)等消极社会经历的参与者,其表观遗传衰老得分显著加速。调整后的模型发现,积极社会经历的总和与减速的表观遗传衰老得分相关(GrimAge β = - 0.431,标准误 = 0.109,p < 0.001;达尼丁β = - 0.009,标准误 = 0.003,p < 0.01),消极社会经历的总和与加速的表观遗传衰老得分相关(GrimAge β = 0.934,标准误 = 0.162,p < 0.001;达尼丁β = 0.015,标准误 = 0.004,p < 0.01)。积极与消极社会经历的“净正”比例的受访者,其GrimAge得分平均比具有“净负”社会经历的受访者年轻4.63岁(β = - 4.729;标准误 = 0.507;p < 0.001;包括协变量的调整后β = - 2.847;标准误 = 0.469;p < 0.001)。发现积极和消极社会经历与表观遗传衰老的关联独立于受访者感知的社会支持以及他们的自我评定身心健康。结果表明,消极社会经历加速表观遗传衰老,而积极社会经历则使其减速。消极和积极社会经历各自独立与表观遗传衰老相关,且净积极社会经历与较慢的表观遗传衰老相关。

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