Lifetime trauma exposure and accelerated epigenetic aging among midlife women.

IF 3.2 2区 心理学 Q1 PSYCHOLOGY
Health Psychology Pub Date : 2025-11-01 Epub Date: 2025-06-16 DOI:10.1037/hea0001523
Rebecca C Thurston, Caroline Y Doyle, Cynthia D J Kusters, Yuefang Chang, Karestan Koenen, Pauline Maki, Judith E Carroll
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引用次数: 0

Abstract

Objective: Trauma exposure may be linked to accelerated biological aging. However, studies have largely considered childhood abuse, with limited consideration of lifetime trauma exposure, particularly for women. Furthermore, few studies have considered newer epigenetic clocks, which have enhanced links with health outcomes. Among midlife women, we investigated whether lifetime trauma exposure is associated with older epigenetic age with several generations of clocks. We explored associations between childhood maltreatment and epigenetic age and racial differences in associations between trauma and epigenetic age.

Method: Two hundred sixteen women (Mage = 59 years, 83% non-Hispanic White, 13% Black, and 4% other race/ethnicities) underwent physical measures, questionnaires to assess lifetime trauma exposure, and a blood draw. A subset of 123 women completed childhood maltreatment measures. Extrinsic epigenetic age, GrimAge, principal component-based PhenoAge, and DunedinPACE were calculated. Clocks were residualized for age and Z-scored for analysis. Associations between trauma and epigenetic age were estimated in linear regression (covariates race, education, body mass index, and estimated cell counts). Interactions by race were tested.

Results: Relative to women without trauma exposure, those with ≥ 2 lifetime traumas had older epigenetic age, GrimAge, 1: B (SE) = 0.15 (0.15), p = .31, 2+: B (SE) = 0.39 (0.13), p = .004; DunedinPACE, 1: B (SE) = 0.23 (0.12), p = .07, 2+: B (SE) = 0.33 (0.11), p = .003. Childhood sexual abuse was also associated with older epigenetic age, GrimAge: B (SE) = 0.56 (0.24), p = .021. Exploratory models suggested that trauma was related to epigenetic age primarily among Black women.

Conclusion: Among midlife women, greater lifetime trauma and possibly childhood sexual abuse were associated with older epigenetic age, independent of chronologic age. Black women may be particularly affected. (PsycInfo Database Record (c) 2025 APA, all rights reserved).

中年妇女终身创伤暴露与加速表观遗传衰老。
目的:创伤暴露可能与生物老化加速有关。然而,研究主要是考虑儿童虐待,很少考虑终身创伤暴露,特别是对妇女。此外,很少有研究考虑到更新的表观遗传时钟,它与健康结果的联系有所增强。在中年妇女中,我们研究了终身创伤暴露是否与几代时钟的表观遗传年龄有关。我们探讨了儿童虐待与表观遗传年龄之间的关系,以及创伤与表观遗传年龄之间的种族差异。方法:216名女性(年龄59岁,83%为非西班牙裔白人,13%为黑人,4%为其他种族/民族)接受了身体测量、评估终身创伤暴露的问卷调查和抽血。123名妇女完成了儿童虐待措施。计算了外在表观遗传年龄、GrimAge、基于主成分的表型年龄和DunedinPACE。时钟对年龄和z评分进行了残差分析。创伤与表观遗传年龄之间的关联通过线性回归(协变量为种族、教育程度、体重指数和估计细胞计数)进行估计。测试了种族间的相互作用。结果:与无创伤暴露的女性相比,有≥2次终身创伤的女性表观遗传年龄较大,grmage, 1: B (SE) = 0.15 (0.15), p = 0.31, 2+: B (SE) = 0.39 (0.13), p = 0.004;DunedinPACE, 1: B (SE) = 0.23 (0.12), p = . 07, 2 +: B (SE) = 0.33 (0.11), p = .003。儿童期性侵也与表观遗传年龄较大相关,grmage: B (SE) = 0.56 (0.24), p = 0.021。探索性模型表明,创伤主要与黑人女性的表观遗传年龄有关。结论:在中年妇女中,较大的终身创伤和可能的儿童期性虐待与较大的表观遗传年龄相关,而与实际年龄无关。黑人女性可能受到的影响尤其严重。(PsycInfo Database Record (c) 2025 APA,版权所有)。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Health Psychology
Health Psychology 医学-心理学
CiteScore
4.90
自引率
2.40%
发文量
170
审稿时长
4-8 weeks
期刊介绍: Health Psychology publishes articles on psychological, biobehavioral, social, and environmental factors in physical health and medical illness, and other issues in health psychology.
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