Beatty Moody Danielle L, Leibel Daniel K, Darden Taylor M, Ashe Jason J, Waldstein Shari R, Katzel Leslie I, Liu Hans B, Weng Nan-Ping, Evans Michele K, Zonderman Alan B
Department of Psychology, University of Maryland, Baltimore County, Baltimore, MD, USA.
Department of Psychology, University of Maryland, Baltimore County, Baltimore, MD, USA.
Biol Psychol. 2019 Feb;141:1-9. doi: 10.1016/j.biopsycho.2018.12.004. Epub 2018 Dec 13.
Studies have linked self-reported discrimination to telomere attrition, a biological marker of accelerated cellular aging. However, it is unknown whether intersections between social categories-race, socioeconomic status (SES), sex, and age-influence the association of varying forms of discrimination with telomere length. We examined these associations in a socioeconomically and racially/ethnically diverse urban sample.
Cross-sectional data were from 341 middle-aged (30-64 years) African American and White, community participants in the Healthy Aging in Neighborhoods of Diversity across the Life Span Study (HANDLS). Multiple regression models examined up to 3-way interactions between a discrimination measure (i.e., everyday, racial, gender, lifetime burden, and frequency of discrimination across sources) and two social categories.
After adjusting for depressive symptoms, waist circumference, and lifetime substance use, two themes emerged: 1) among women with higher SES, a) greater lifetime discrimination burden (b = -0.23, p = .011), gender discrimination (b = -0.29, p = .040), and racial discrimination (b = -0.24, p = 0.023) and 2) among younger adults, irrespective of race and sex, greater frequency of discrimination across sources (b = 0.002, p = .008) was associated with shorter telomeres.
Irrespective of race, women with higher SES and younger adults reporting greater discrimination may be at particular risk for accelerated aging. Telomere attrition promotes and accelerates chronic health conditions for which there are health disparities. Future research explicating intersections among specific discrimination indices and social categories is warranted.
研究已将自我报告的歧视与端粒损耗联系起来,端粒损耗是细胞加速衰老的生物学标志物。然而,社会类别(种族、社会经济地位(SES)、性别和年龄)之间的交叉是否会影响不同形式的歧视与端粒长度之间的关联尚不清楚。我们在一个社会经济和种族/民族多样化的城市样本中研究了这些关联。
横断面数据来自341名中年(30 - 64岁)非裔美国人和白人社区参与者,他们参与了“全生命周期多元社区健康老龄化研究”(HANDLS)。多元回归模型检验了一种歧视测量指标(即日常、种族、性别、终生负担以及不同来源的歧视频率)与两个社会类别之间高达三向的相互作用。
在对抑郁症状、腰围和终生物质使用情况进行调整后,出现了两个主题:1)在社会经济地位较高的女性中,a)更大的终生歧视负担(b = -0.23,p = 0.011)、性别歧视(b = -0.29,p = 0.040)和种族歧视(b = -0.24,p = 0.023);2)在年轻人中,无论种族和性别,不同来源的歧视频率更高(b = 0.002,p = 0.008)与较短的端粒相关。
无论种族如何,社会经济地位较高且报告遭受更多歧视的女性以及年轻人可能尤其面临加速衰老的风险。端粒损耗会促进并加速存在健康差异的慢性健康状况。未来有必要开展研究以阐明特定歧视指标与社会类别之间的交叉情况。