Hailu Elleni M, Lewis Tené T, Needham Belinda L, Lin Jue, Seeman Teresa E, Mujahid Mahasin S
Division of Epidemiology, School of Public Health, University of California Berkeley, USA.
Department of Epidemiology, Rollins School of Public Health, Emory University, Atlanta, Georgia, USA.
J Gerontol A Biol Sci Med Sci. 2021 Jul 20. doi: 10.1093/gerona/glab193.
We aimed to examine if neighborhood social cohesion moderated longitudinal associations between baseline reports of discrimination and 10-year changes in leukocyte telomere length (LTL).
Data are from the Multi-Ethnic Study of Atherosclerosis (N = 1064; age range 45-84 years). Baseline discrimination was measured using the Major Experiences of Discrimination Scale (MDS; none, 1 domain, ≥2 domains) and the Experiences of Discrimination Scale (EDS; none, moderate, high). Neighborhood social cohesion at baseline was assessed via a community survey within census tract-defined neighborhoods. 10-year change in LTL was defined as regression to the mean-corrected 10-year difference in the ratio of telomeric DNA to a single-copy gene (T/S).
In linear mixed-effects models, we found that neighborhood social cohesion modified the effect of baseline reports of MDS on 10-year changes in LTL, independent of sociodemographic characteristics, health behaviors, and health conditions (p(χ 2) = .01). Among those residing in neighborhoods with low social cohesion, experiencing major discrimination in ≥2 domains was associated with faster LTL attrition over 10 years, compared to reporting no discrimination (β = -0.03; 95% confidence interval: -0.06, -0.003). We found no main associations for either discrimination measure and no interaction between EDS and neighborhood social cohesion.
Results indicate that neighborhood social cohesion is an important dimension of the neighborhood context that may moderate the impact of major experiences of discrimination on telomere length attrition. These findings help advance our understanding of the integral role that neighborhood environments play in attenuating the effect of discrimination on accelerated cell aging.
我们旨在研究邻里社会凝聚力是否会调节基线时的歧视报告与白细胞端粒长度(LTL)10年变化之间的纵向关联。
数据来自动脉粥样硬化多族裔研究(N = 1064;年龄范围45 - 84岁)。使用歧视主要经历量表(MDS;无、1个领域、≥2个领域)和歧视经历量表(EDS;无、中度、高度)测量基线时的歧视情况。通过在人口普查区界定的邻里内进行的社区调查评估基线时的邻里社会凝聚力。LTL的10年变化定义为端粒DNA与单拷贝基因(T/S)比率的均值校正10年差异的回归。
在线性混合效应模型中,我们发现邻里社会凝聚力改变了MDS基线报告对LTL 10年变化的影响,独立于社会人口学特征、健康行为和健康状况(p(χ 2) = .01)。在社会凝聚力低的邻里中居住的人群中,与报告无歧视相比,在≥2个领域经历主要歧视与10年内更快的LTL损耗相关(β = -0.03;95%置信区间:-0.06,-0.003)。我们未发现任何一种歧视测量方法的主要关联,也未发现EDS与邻里社会凝聚力之间的相互作用。
结果表明,邻里社会凝聚力是邻里环境的一个重要维度,可能会调节主要歧视经历对端粒长度损耗的影响。这些发现有助于推进我们对邻里环境在减轻歧视对加速细胞衰老影响方面所起的整体作用的理解。