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首页> 外文期刊>Scientific reports. >Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus
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Association of a rare variant of the TNFSF13B gene with susceptibility to Rheumatoid Arthritis and Systemic Lupus Erythematosus

机译:TNFSF13B基因的罕见变体与类风湿关节炎和系统性红斑狼疮的易感性相关

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A rare variant (BAFF-var) of the tumor necrosis factor superfamily 13b (TNFSF13B) gene has been recently associated with multiple sclerosis (MS) and systemic lupus erythematosus (SLE). The aim of this study was to investigate the association between TNFSF13B BAFF-var and susceptibility to rheumatoid arthritis (RA) and replicate that association in SLE. 6,218 RA patients, 2,575 SLE patients and 4,403 healthy controls from three different countries were included in the study. TNFSF13B BAFF-var was genotyped using TaqMan allelic discrimination assay. PLINK software was used for statistical analyses. TNFSF13B BAFF-var was significantly associated with RA (p?=?0.015, OR?=?1.21, 95% CI?=?1.03–1.41) in the Spanish cohort. A trend of association was observed in the Dutch (p?=?0.115) and German (p?=?0.228) RA cohorts. A meta-analysis of the three RA cohorts included in this study revealed a statistically significant association (p?=?0.002, OR?=?1.24, 95% CI?=?1.10–1.38). In addition, TNFSF13B BAFF-var was significantly associated with SLE in the Spanish (p?=?0.001, OR?=?1.41, 95% CI?=?1.14–1.74) and the German cohorts (p?=?0.030, OR?=?1.86, 95% CI?=?1.05–3.28), with a statistically significant p-value obtained in the meta-analysis (p?=?0.0002, OR?=?1.46, 95% CI?=?1.09–2.32). The results obtained confirm the known association of TNFSF13B BAFF-var with SLE and, for the first time, demonstrate that this variant contributes to susceptibility to RA.
机译:肿瘤坏死因子超家族13b(TNFSF13B)基因的罕见变体(BAFF-var)最近与多发性硬化症(MS)和系统性红斑狼疮(SLE)相关。这项研究的目的是调查TNFSF13B BAFF-var与类风湿关节炎(RA)的敏感性之间的关联,并在SLE中复制该关联。研究包括来自三个不同国家的6,218名RA患者,2,575名SLE患者和4,403名健康对照。使用TaqMan等位基因鉴别分析对TNFSF13B BAFF-var进行基因分型。使用PLINK软件进行统计分析。在西班牙人群中,TNFSF13B BAFF-var与RA显着相关(p = 0.015,OR = 1.21,95%CI = 1.03-1.41)。在荷兰(p?=?0.115)和德国(p?=?0.228)RA队列中观察到关联趋势。对本研究中包括的三个RA队列的荟萃分析显示出统计学上的显着相关性(p = 0.002,OR = 1.24,95%CI = 1.10-1.38)。此外,TNFSF13B BAFF-var与西班牙人(p?=?0.001,OR?=?1.41,95%CI?=?1.14-1.74)和德国人群(p?=?0.030,OR)的SLE显着相关。 ?=?1.86,95%CI?=?1.05-3.28),在荟萃分析中获得具有统计学意义的p值(p?=?0.0002,OR?=?1.46,95%CI?=?1.09– 2.32)。获得的结果证实了TNFSF13B BAFF-var与SLE的已知关联,并首次证明该变异有助于RA的易感性。

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