Multi-discrimination exposure and biological aging: Results from the midlife in the United States study

IF 3.7 Q2 IMMUNOLOGY Brain, behavior, & immunity - health Pub Date : 2024-05-09 DOI:10.1016/j.bbih.2024.100774
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Abstract

Discrimination is a social determinant of health and health disparities for which the biological mechanisms remain poorly understood. This study investigated the hypothesis that discrimination contributes to poor health outcomes by accelerating biological processes of aging. We analyzed survey and blood DNA methylation data from the Midlife in the United States (MIDUS) study (N = 1967). We used linear regression analysis to test associations of everyday, major, and workplace discrimination with biological aging measured by the DunedinPACE, PhenoAge, and GrimAge2 epigenetic clocks. MIDUS participants who reported more discrimination tended to exhibit a faster pace of aging and older biological age as compared to peers who reported less discrimination. Effect-sizes for associations tended to be larger for the DunedinPACE pace-of-aging clock (effect-size range r = 0.1–0.2) as compared with the PhenoAge and GrimAge2 biological-age clocks (effect-sizes r < 0.1) and for experiences of everyday and major discrimination as compared with workplace discrimination. Smoking status and body-mass index accounted for roughly half of observed association between discrimination and biological aging. Reports of discrimination were more strongly associated with accelerated biological aging among White as compared with Black participants, although Black participants reported more discrimination overall and tended to exhibit older biological age and faster biological aging. Findings support the hypothesis that experiences of interpersonal discrimination contribute to accelerated biological aging and suggest that structural and individual-level interventions to reduce discrimination and promote adaptive coping have potential to support healthy aging and build health equity.

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多重歧视与生物衰老:美国中年研究的结果
歧视是健康和健康差异的一个社会决定因素,其生物学机制至今仍鲜为人知。本研究探讨了歧视通过加速生物衰老过程导致不良健康结果的假设。我们分析了美国中年(MIDUS)研究(N = 1967)中的调查和血液 DNA 甲基化数据。我们使用线性回归分析来检验日常歧视、重大歧视和工作场所歧视与通过 DunedinPACE、PhenoAge 和 GrimAge2 表观遗传时钟测量的生物衰老之间的关联。与受歧视较少的人相比,受歧视较多的 MIDUS 参与者往往老化速度更快,生理年龄更大。与 PhenoAge 和 GrimAge2 生物年龄时钟(效应大小 r <0.1)相比,DunedinPACE 衰老速度时钟(效应大小范围 r = 0.1-0.2)的关联效应大小往往更大;与工作场所歧视相比,日常和重大歧视经历的关联效应大小往往更大。吸烟状况和体重指数约占所观察到的歧视与生物衰老之间关联的一半。与黑人受试者相比,白人受试者的歧视报告与加速生物衰老的关系更为密切,尽管黑人受试者报告的歧视总体上更多,而且往往表现出更老的生物年龄和更快的生物衰老。研究结果支持人际歧视导致生物衰老加速的假设,并表明减少歧视和促进适应性应对的结构性和个人层面的干预措施有可能支持健康老龄化和建立健康公平。
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来源期刊
Brain, behavior, & immunity - health
Brain, behavior, & immunity - health Biological Psychiatry, Behavioral Neuroscience
CiteScore
8.50
自引率
0.00%
发文量
0
审稿时长
97 days
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