Cuevas Adolfo G, Freilich Colin D, Mann Frank D, Cole Steve W, Krueger Robert F
Department of Social and Behavioral Sciences, School of Global Public Health, New York University, United States.
Department of Psychology, University of Minnesota, United States.
Brain Behav Immun Health. 2022 Dec 30;27:100580. doi: 10.1016/j.bbih.2022.100580. eCollection 2023 Feb.
Addressing social disparities in health and well-being requires understanding how the effects of discrimination become biologically embedded, and how embedding processes might vary across different demographic contexts. Emerging research suggests that a threat-related gene expression response may contribute to social disparities in health. We tested a contextual vulnerability model of discrimination embedding using an empirical intersectionality (interaction discovery) analysis of pro-inflammatory gene expression in a national sample of non-institutionalized, English-speaking adults with RNA biomarker data (n = 543). At the time of data collection, the average age of participants was 55 years (SD = 13.26) and approximately half identified as female (50.46%). Most participants identified as White (∼73%) and had some college experience (∼60%). Results showed significant variation in the strength of association between daily discrimination and inflammatory gene expression by race and sex ( = -0.022; 95% CI:-0.038,-0.005, = .009) with the estimated marginal association larger for racially-minoritized males ( = 0.007; 95% CI:-0.003,0.017, = .163), compared to White males ( = -0.006; 95% CI:-0.013,0.001, = .076). This study indicates that the link between daily discrimination and inflammatory gene expression may vary by sociodemographic characteristics. To improve initiatives and policies aimed at ameliorating disparities within populations, greater attention is needed to understand how interlocking systems of inequalities contribute to physiological health.
解决健康和福祉方面的社会差异需要了解歧视的影响是如何在生物学层面扎根的,以及这种扎根过程在不同人口背景下可能会有怎样的差异。新兴研究表明,与威胁相关的基因表达反应可能导致健康方面的社会差异。我们使用经验性交叉性(交互作用发现)分析方法,对一个全国性的非机构化、说英语的成年人样本(n = 543)的促炎基因表达进行了测试,该样本具有RNA生物标志物数据,以此来检验歧视扎根的情境脆弱性模型。在数据收集时,参与者的平均年龄为55岁(标准差 = 13.26),约一半的人认定为女性(50.46%)。大多数参与者认定为白人(约73%),并且有一些大学经历(约60%)。结果显示,按种族和性别划分,日常歧视与炎症基因表达之间的关联强度存在显著差异(β = -0.022;95%置信区间:-0.038,-0.005,p = 0.009),与白人男性(β = -0.006;95%置信区间:-0.013,0.001,p = 0.076)相比,种族少数群体男性的估计边际关联更大(β = 0.007;95%置信区间:-0.003,0.017,p = 0.163)。这项研究表明,日常歧视与炎症基因表达之间的联系可能因社会人口特征而异。为了改进旨在改善人群内部差异的举措和政策,需要更多关注来了解不平等的相互关联系统是如何影响生理健康的。