Major experiences of perceived discrimination across life and biological aging

IF 3.6 2区 医学 Q2 ENDOCRINOLOGY & METABOLISM Psychoneuroendocrinology Pub Date : 2025-04-01 Epub Date: 2025-02-03 DOI:10.1016/j.psyneuen.2025.107380
Roma Dhingra , Abby R. Hillmann , Rebecca G. Reed
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Abstract

Perceived lifetime discrimination may accelerate aspects of biological aging, but it is unknown whether there are life stages during which experiencing discrimination has the greatest biological impacts. In this study, we tested the effects of total forms of perceived lifetime discrimination experienced both across life and in specific lifespan stages on biological aging. Health and Retirement Study participants (N = 2986, Mage=68 years, 46.2 % Male, 73.4 % White) reported most recent experiences of perceived lifetime discrimination events and their years of occurrence; events were summed across one’s life (total forms of perceived lifetime discrimination across life) and in the following life stages: childhood (0–17 years), young adulthood (18−39), midlife (40−59), and late adulthood (60 +). Blood drawn after survey completion (average 5.89 years later) was used to measure biological aging outcomes, including inflammation (CRP, IL-6, and sTNFR-1) and epigenetic age. In multilevel models adjusted for age, sex, BMI, smoking status, and the time interval between completing the discrimination questionnaire and blood draw, those who experienced greater total forms of perceived lifetime discrimination had higher levels of CRP (γ=0.08, p < 0.001) and IL-6 (γ=0.07, p < 0.001). When testing each life stage in separate models, more perceived lifetime discrimination events in young adulthood were associated with higher IL-6 (γ=0.05, p = 0.015). When comparing the effects of the life stages within the same model among adults age 45 + (n = 2978), more perceived lifetime discrimination events in young adulthood were independently associated with higher IL-6 (γ=0.07, p = 0.001) and in midlife with higher CRP (γ=0.06, p = 0.011) and IL-6 (γ=0.07, p = 0.002). Perceived lifetime discrimination was not associated with sTNFR-1 or epigenetic age. More perceived lifetime discrimination events – both across one’s life and in certain adult developmental life stages – are associated with higher levels of later-life inflammation. In particular, young adulthood and midlife may be sensitive periods during which experiencing perceived lifetime discrimination has the greatest immunological impacts.
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在生命和生物衰老过程中感知歧视的主要经历
感知到的终生歧视可能会加速生物衰老的各个方面,但尚不清楚是否存在经历歧视的生命阶段具有最大的生物影响。在这项研究中,我们测试了在整个生命和特定生命阶段经历的感知生命歧视的总形式对生物衰老的影响。健康与退休研究的参与者(N = 2986,年龄为68岁,男性46.2% %,白人73.4 %)报告了最近一次感知到的终身歧视事件的经历及其发生年份;事件在一个人的一生中(一生中感知到的一生歧视的总形式)和以下生命阶段进行总结:童年(0-17岁)、青年(18 - 39岁)、中年(40 - 59岁)和成年晚期(60岁 +)。调查结束后(平均5.89年)抽血用于测量生物学衰老结果,包括炎症(CRP、IL-6和sTNFR-1)和表观遗传年龄。在调整了年龄、性别、BMI、吸烟状况和完成歧视问卷与抽血之间的时间间隔的多水平模型中,那些感知到终生歧视的总形式更大的人有更高的CRP (γ=0.08, p <; 0.001)和IL-6 (γ=0.07, p <; 0.001)水平。当在单独的模型中测试每个生命阶段时,青年期更多的感知生命期歧视事件与较高的IL-6相关(γ=0.05, p = 0.015)。当比较的影响45岁成年人生命阶段在同一个模型 + (n = 2978),更认为一生歧视发生在成年早期高出独立与il - 6(γ= 0.07,p = 0.001)和中年高c反应蛋白(γ= 0.06,p = 0.011)和il - 6(γ= 0.07,p = 0.002)。感知到的终生歧视与sTNFR-1或表观遗传年龄无关。在一个人的一生中以及在某些成年发展阶段,更多的感知到的终身歧视事件与晚年炎症的高水平有关。特别是,青年和中年可能是敏感时期,在此期间经历感知到的终身歧视具有最大的免疫影响。
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来源期刊
Psychoneuroendocrinology
Psychoneuroendocrinology 医学-精神病学
CiteScore
7.40
自引率
8.10%
发文量
268
审稿时长
66 days
期刊介绍: Psychoneuroendocrinology publishes papers dealing with the interrelated disciplines of psychology, neurobiology, endocrinology, immunology, neurology, and psychiatry, with an emphasis on multidisciplinary studies aiming at integrating these disciplines in terms of either basic research or clinical implications. One of the main goals is to understand how a variety of psychobiological factors interact in the expression of the stress response as it relates to the development and/or maintenance of neuropsychiatric illnesses.
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