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我也是美国人:对非裔美国人系统性红斑狼疮研究的综述。

I too, am America: a review of research on systemic lupus erythematosus in African-Americans.

机构信息

Division of Rheumatology, Department of Public Health Sciences, Medicine, MUSC Center for Health Disparities Research, Medical University of South Carolina , Charleston, South Carolina , USA.

Arnold School of Public Health, University of South Carolina , Columbia, South Carolina , USA.

出版信息

Lupus Sci Med. 2016 Aug 24;3(1):e000144. doi: 10.1136/lupus-2015-000144. eCollection 2016.

Abstract

Systemic lupus erythematosus (SLE) is a multi-organ autoimmune disorder that can cause significant morbidity and mortality. A large body of evidence has shown that African-Americans experience the disease more severely than other racial-ethnic groups. Relevant literature for the years 2000 to August 2015 were obtained from systematic searches of PubMed, Scopus, and the EBSCOHost platform that includes MEDLINE, CINAHL, etc. to evaluate research focused on SLE in African-Americans. Thirty-six of the 1502 articles were classified according to their level of evidence. The systematic review of the literature reported a wide range of adverse outcomes in African-American SLE patients and risk factors observed in other mono and multi-ethnic investigations. Studies limited to African-Americans with SLE identified novel methods for more precise ascertainment of risk and observed novel findings that hadn't been previously reported in African-Americans with SLE. Both environmental and genetic studies included in this review have highlighted unique African-American populations in an attempt to isolate risk attributable to African ancestry and observed increased genetic influence on overall disease in this cohort. The review also revealed emerging research in areas of quality of life, race-tailored interventions, and self-management. This review reemphasizes the importance of additional studies to better elucidate the natural history of SLE in African-Americans and optimize therapeutic strategies for those who are identified as being at high risk.

摘要

系统性红斑狼疮(SLE)是一种多器官自身免疫性疾病,可导致严重的发病率和死亡率。大量证据表明,非裔美国人比其他种族群体更易患此病。从 2000 年到 2015 年 8 月,通过对 PubMed、Scopus 和 EBSCOHost 平台(包括 MEDLINE、CINAHL 等)的系统搜索,获取了相关文献,以评估针对非裔美国人的 SLE 研究。根据证据水平,将 1502 篇文章中的 36 篇进行了分类。文献系统评价报告称,非裔美国 SLE 患者存在广泛的不良结局和其他单民族及多民族研究中观察到的风险因素。仅针对非裔美国 SLE 患者的研究确定了更精确确定风险的新方法,并观察到了以前在非裔美国 SLE 患者中未报告的新发现。本综述中包含的环境和遗传研究都强调了独特的非裔美国人人群,试图将归因于非洲血统的风险孤立出来,并观察到该队列中整体疾病的遗传影响增加。该综述还揭示了在生活质量、针对种族的干预措施和自我管理等领域的新兴研究。本综述再次强调了开展更多研究的重要性,以更好地阐明非裔美国人 SLE 的自然病史,并优化被认为处于高风险的患者的治疗策略。

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