Authors' Affiliations: Cancer Epidemiology and Health Services Research Group, Centre for Public Health, Queen's University Belfast, Belfast, Northern Ireland; Multiple Myeloma Section, National Cancer Institute, NIH, Bethesda, Maryland; and Centre for Population Health, Department of Social and Preventive Medicine, Faculty of Medicine, University of Malaya, Kuala Lumpur, Malaysia.
Cancer Epidemiol Biomarkers Prev. 2014 Feb;23(2):332-42. doi: 10.1158/1055-9965.EPI-13-0695. Epub 2014 Jan 22.
Several observational studies have investigated autoimmune disease and subsequent risk of monoclonal gammopathy of undetermined significance (MGUS) and multiple myeloma. Findings have been largely inconsistent and hindered by the rarity and heterogeneity of the autoimmune disorders investigated. A systematic review of the literature was undertaken to evaluate the strength of the evidence linking prior autoimmune disease and risk of MGUS/multiple myeloma.
A broad search strategy using key terms for MGUS, multiple myeloma, and 50 autoimmune diseases was used to search four electronic databases (PubMed, Medline, Embase, and Web of Science) from inception through November 2011.
A total of 52 studies met the inclusion criteria, of which 32 were suitably comparable to perform a meta-analysis. "Any autoimmune disorder" was associated with an increased risk of both MGUS [n = 760 patients; pooled relative risk (RR) 1.42; 95% confidence interval (CI), 1.14-1.75] and multiple myeloma (n>2,530 patients; RR 1.13, 95% CI, 1.04-1.22). This risk was disease dependent with only pernicious anemia showing an increased risk of both MGUS (RR 1.67; 95% CI, 1.21-2.31) and multiple myeloma (RR 1.50; 95% CI, 1.25-1.80).
Our findings, based on the largest number of autoimmune disorders and patients with MGUS/multiple myeloma reported to date, suggest that autoimmune diseases and/or their treatment may be important in the etiology of MGUS/multiple myeloma. The strong associations observed for pernicious anemia suggest that anemia seen in plasma cell dyscrasias may be of autoimmune origin.
Underlying mechanisms of autoimmune diseases, general immune dysfunction, and/or treatment of autoimmune diseases may be important in the pathogenesis of MGUS/multiple myeloma.
已有几项观察性研究调查了自身免疫性疾病与意义未明的单克隆丙种球蛋白血症(MGUS)和多发性骨髓瘤随后发病风险之间的关系。但由于所研究的自身免疫性疾病罕见且存在异质性,这些研究的结果大多不一致,难以定论。我们进行了系统的文献回顾,以评估将既往自身免疫性疾病与 MGUS/多发性骨髓瘤发病风险联系起来的证据强度。
我们使用 MGUS、多发性骨髓瘤和 50 种自身免疫性疾病的关键词制定了广泛的搜索策略,从创建数据库起至 2011 年 11 月在四个电子数据库(PubMed、Medline、Embase 和 Web of Science)中进行了搜索。
共有 52 项研究符合纳入标准,其中 32 项研究适合进行荟萃分析。“任何自身免疫性疾病”均与 MGUS(n = 760 例患者;汇总相对危险度 [RR] 1.42;95%置信区间 [CI],1.14-1.75)和多发性骨髓瘤(n>2,530 例患者;RR 1.13,95%CI,1.04-1.22)发病风险增加相关。这种风险与疾病相关,只有恶性贫血显示出 MGUS(RR 1.67;95%CI,1.21-2.31)和多发性骨髓瘤(RR 1.50;95%CI,1.25-1.80)发病风险均增加。
我们的研究结果基于迄今为止报道的数量最多的自身免疫性疾病和 MGUS/多发性骨髓瘤患者,提示自身免疫性疾病和/或其治疗可能在 MGUS/多发性骨髓瘤的病因学中起重要作用。恶性贫血观察到的强关联表明浆细胞异常增生症中出现的贫血可能为自身免疫性原因。
自身免疫性疾病的潜在机制、一般免疫功能障碍和/或自身免疫性疾病的治疗可能在 MGUS/多发性骨髓瘤的发病机制中起重要作用。