Population Research Center, The University of Texas at Austin, 305 E. 23(rd) Street, Stop G1800, RLP 2.602, Austin, TX 78712, United States.
Department of Human Development and Family Studies, Michigan State University, 552 W. Circle Drive, Human Ecology, 13C, East Lansing, MI 48824, United States.
Brain Behav Immun. 2023 Aug;112:77-84. doi: 10.1016/j.bbi.2023.06.004. Epub 2023 Jun 5.
Racial discrimination is a distinct health threat that increases disease risk among Black Americans. Psychosocial stress may compromise health through inflammatory mechanisms. This study examines incident experiences of racial discrimination and changes in the inflammatory biomarker C-reactive protein (CRP) over a two-year period among Black women with systemic lupus erythematosus (SLE)-an inflammatory autoimmune disease sensitive to psychosocial stress and characterized by stark racial inequities in outcomes.
Data are from the Black Women's Experiences Living with Lupus (BeWELL) Study. Participants (n = 380) from metropolitan Atlanta, Georgia were enrolled from April 2015 to May 2017. Incident racial discrimination was assessed bi-annually via self-report using the Experiences of Discrimination measure. CRP was assessed annually over a two-year period. Latent change score analyses modeled longitudinal within-person associations between incident racial discrimination and change in log-transformed CRP from baseline to Year 2.
Incident experiences of racial discrimination were associated with elevated log-CRP across the two-year study period (b = 0.039, SE = 0.017, 95% CI: 0.006, 0.071). For each domain of incident racial discrimination experienced, CRP increased 3.98%.
This study contributes to growing evidence on the biological consequences of racism and is the first to document an association between incident racial discrimination and changes in inflammation among Black women with SLE. Racial inequities in SLE outcomes and other diseases driven by inflammatory pathways may be explained in part through experiences of racial discrimination.
种族歧视是一个明显的健康威胁,它会增加美国黑人的疾病风险。心理社会压力可能通过炎症机制损害健康。本研究考察了系统性红斑狼疮(SLE)黑人女性在两年内经历的种族歧视事件和炎症生物标志物 C 反应蛋白(CRP)的变化,SLE 是一种对心理社会压力敏感的炎症性自身免疫性疾病,其结果存在明显的种族差异。
数据来自《黑人女性狼疮生活体验研究》(BeWELL 研究)。参与者(n=380)来自佐治亚州亚特兰大的都会区,于 2015 年 4 月至 2017 年 5 月期间入组。通过使用歧视经历量表(Experiences of Discrimination measure),每两年通过自我报告评估一次新出现的种族歧视。在两年的研究期间,每年评估一次 CRP。潜变量变化得分分析模型模拟了新出现的种族歧视与从基线到第 2 年期间 CRP 对数变化的纵向个体内关联。
在两年的研究期间,新出现的种族歧视经历与 CRP 升高相关(b=0.039,SE=0.017,95%置信区间:0.006,0.071)。经历的每一种新的种族歧视事件,CRP 都会增加 3.98%。
本研究为种族主义的生物学后果提供了更多的证据,并且是第一个记录新出现的种族歧视与 SLE 黑人女性炎症变化之间关联的研究。SLE 结果和其他炎症途径驱动的疾病中的种族差异部分可以通过种族歧视经历来解释。