红斑狼疮的差异与健康的社会决定因素的作用:知识现状与未来研究方向》。

ACR Open Rheumatology Pub Date : 2023-09-01 Epub Date: 2023-08-02 DOI:10.1002/acr2.11590
Joy Buie, Emma McMillan, Jillian Kirby, Leigh Ann Cardenas, Sanaz Eftekhari, Candace H Feldman, Cyrena Gawuga, Andrea M Knight, S Sam Lim, Sheryl McCalla, Daria McClamb, Barbara Polk, Edith Williams, Ed Yelin, Sanoja Shah, Karen H Costenbader
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引用次数: 0

摘要

系统性红斑狼疮(SLE)是一种慢性自身免疫性疾病。在影响系统性红斑狼疮及其病程的过程中,种族、民族和健康的社会决定因素(SDOH)之间的复杂关系日益受到重视。多种社会决定健康因素与狼疮的发病率和预后密切相关,并导致狼疮的健康差异。在美国,社会经济地位的衡量标准,包括经济不稳定、贫困、失业和食品不安全,以及邻里和建筑环境的特征,包括缺乏安全和负担得起的住房、犯罪、压力、种族隔离和歧视,都与种族和民族有关,是导致狼疮不良后果的风险因素。美国狼疮基金会的健康差异顾问小组由10位健康差异专家组成,其中包括学术研究人员和患者,他们在18个月的时间里召开了12次会议,为本研究收集和审查数据。资料来源包括 2011 年至 2023 年在 PubMed 上发表的文章、美国疾病控制和预防中心的数据以及参考书目和建议。搜索关键词包括狼疮、种族、民族和 SDOH 领域。数据经提取和综合后形成本科学声明。较贫穷的社区与损害增加、护理减少和压力引起的狼疮复发相关。美国在医疗保健的可负担性、可获得性和可接受性方面存在巨大差异,这些差异因地区、保险状况、种族和少数民族群体而异。初步的干预措施以社会支持、抑郁和共同决策为目标,但还需要更多的研究、干预措施的实施和评估。红斑狼疮在美国不同种族和族裔群体中的差异是由 SDOH 造成的,其中一些因素比其他因素更容易补救。要应对这些复杂的挑战、缩小差距并改善疗效,就需要采取多维度、多学科的方法,让各利益相关群体参与其中。
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Disparities in Lupus and the Role of Social Determinants of Health: Current State of Knowledge and Directions for Future Research.

Systemic lupus erythematosus (SLE) is a chronic autoimmune disease. The complex relationships between race and ethnicity and social determinants of health (SDOH) in influencing SLE and its course are increasingly appreciated. Multiple SDOH have been strongly associated with lupus incidence and outcomes and contribute to health disparities in lupus. Measures of socioeconomic status, including economic instability, poverty, unemployment, and food insecurity, as well as features of the neighborhood and built environment, including lack of safe and affordable housing, crime, stress, racial segregation, and discrimination, are associated with race and ethnicity in the US and are risk factors for poor outcomes in lupus. In this scientific statement, we aimed to summarize current evidence on the role of SDOH in relation to racial and ethnic disparities in SLE and SLE outcomes, primarily as experienced in the U.S. Lupus Foundation of America's Health Disparities Advisory Panel, comprising 10 health disparity experts, including academic researchers and patients, who met 12 times over the course of 18 months in assembling and reviewing the data for this study. Sources included articles published from 2011 to 2023 in PubMed, Centers for Disease Control and Prevention data, and bibliographies and recommendations. Search terms included lupus, race, ethnicity, and SDOH domains. Data were extracted and synthesized into this scientific statement. Poorer neighborhoods correlate with increased damage, reduced care, and stress-induced lupus flares. Large disparities in health care affordability, accessibility, and acceptability exist in the US, varying by region, insurance status, and racial and minority groups. Preliminary interventions targeted social support, depression, and shared-decision-making, but more research and intervention implementation and evaluation are needed. Disparities in lupus across racial and ethnic groups in the US are driven by SDOH, some of which are more easily remediable than others. A multidimensional and multidisciplinary approach involving various stakeholder groups is needed to address these complex challenges, address these diminish disparities, and improve outcomes.

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