Xie Qiao-Mei, Hu Hua-Qing, Li Su-Su, Wang Fang, Zhang Man, Jiang Shan-Qun, Pan Fa-Ming, Su Hong, Zou Yan-Feng
Department of Epidemiology and Biostatistics, School of Public Health, Anhui Medical University, Hefei, 230032, Anhui, China; The Key Laboratory of Anhui Medical Autoimmune Diseases, Hefei, 230032, Anhui, China.
Department of Health Examination Center, The First Affiliated Hospital of Anhui Medical University, Hefei, 230022, Anhui, China.
Microb Pathog. 2019 Feb;127:352-358. doi: 10.1016/j.micpath.2018.12.029. Epub 2018 Dec 17.
Systemic lupus erythematosus (SLE) is a complex, chronic autoimmune disease, and oestrogen is considered to be a predisposing factor for SLE. Although some studies are conducted to explore the association between oestrogen receptor alpha (ERα) gene polymorphisms and SLE susceptibility, their results are inconsistent.
Meta-analysis was conducted to confirm whether ERα gene polymorphisms were associated with SLE susceptibility, and the strength of association was anticipated by pooled ORs with 95% CIs. Stata software package version 12.0 was used to calculate all the statistical analyses.
Twelve studies included 2494 cases and 4176 controls were incorporated in our meta-analysis. A significant association was found for ERα PvuII polymorphism in the overall population (CC+CT vs TT: OR = 1.334, 95% CI = 1.195-1.490, P < 0.001; CC vs TT: OR = 1.401, 95% CI = 1.096-1.791, P = 0.007; CT vs TT: OR = 1.284, 95% CI = 1.141-1.444, P < 0.001; C vs T: OR = 1.221, 95% CI = 1.084-1.375, P = 0.001), while there was no significant association for ERα XbaI polymorphism. Besides, in stratification analyses by ethnicity, the PvuII polymorphism was associated with an increased risk of SLE in Asians (CC+CT vs TT: OR = 1.379, 95% CI = 1.203-1.581, P < 0.001; CT vs TT: OR = 1.308, 95% CI = 1.130-1.515, P < 0.001; C vs T: OR = 1.240, 95% CI = 1.052-1.462, P = 0.010), while for ESR1 XbaI polymorphism, a significantly increased risk of SLE susceptibility was found in Asians (GA vs AA: OR = 1.271, 95% CI = 1.101-1.467, P = 0.001).
Our meta-analysis indicated that the ERα PvuII polymorphism was significantly associated with SLE susceptibility in the overall and Asian populations, while the ERα XbaI GA genotype only played a key role in SLE susceptibility in Asian populations.
系统性红斑狼疮(SLE)是一种复杂的慢性自身免疫性疾病,雌激素被认为是SLE的一个诱发因素。尽管有一些研究探讨了雌激素受体α(ERα)基因多态性与SLE易感性之间的关联,但其结果并不一致。
进行荟萃分析以确认ERα基因多态性是否与SLE易感性相关,并通过合并的比值比(OR)及其95%可信区间(CI)来评估关联强度。使用Stata软件包12.0版进行所有统计分析。
12项研究纳入了2494例病例和4176例对照进行荟萃分析。在总体人群中发现ERα PvuII多态性存在显著关联(CC + CT与TT比较:OR = 1.334,95%CI = 1.195 - 1.490,P < 0.001;CC与TT比较:OR = 1.401,95%CI = 1.096 - 1.791,P = 0.007;CT与TT比较:OR = 1.284,95%CI = 1.141 - 1.444,P < 0.001;C与T比较:OR = 1.221,95%CI = 1.084 - 1.375,P = 0.001),而ERα XbaI多态性无显著关联。此外,在按种族分层分析中,PvuII多态性与亚洲人SLE风险增加相关(CC + CT与TT比较:OR = 1.379,95%CI = 1.203 - 1.581,P < 0.001;CT与TT比较:OR = 1.308,95%CI = 1.130 - 1.515,P < 0.001;C与T比较:OR = 1.240,95%CI = 1.052 - 1.462,P = 0.010),而对于ESR1 XbaI多态性,在亚洲人中发现SLE易感性风险显著增加(GA与AA比较:OR = 1.271,95%CI = 1.101 - 1.467,P = 0.001)。
我们的荟萃分析表明,ERα PvuII多态性在总体人群和亚洲人群中与SLE易感性显著相关,而ERα XbaI GA基因型仅在亚洲人群的SLE易感性中起关键作用。