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Single nucleotide polymorphism rs5029937 in TNFAIP3 gene is correlated with risk of rheumatoid arthritis

机译:TNFAIP3基因中的单核苷酸多态性RS5029937与类风湿性关节炎的风险相关

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摘要

Background: Rheumatoid arthritis (RA) is a progressive and common autoimmune disease with multifactorial etiology. Several pieces of research show that genetic factors play a major role in the incidence of RA. Several genome-wide association studies (GWAS) have identified the tumor necrosis factor alpha inducible protein 3 (TNFAIP3) genes as one of the candidate loci. The TNFAIP3 gene encoding ubiquitin-editing protein A20 witch restricts B cell survival and prevents autoimmunity. Previous studies have indicated that single nucleotide polymorphisms (SNPs) in the TNFAIP3 gene are correlated with several autoimmune disorders. In the present study, we assessed the possible association between SNP rs5029937 (intronic variant) in the TNFAIP3 gene with RA risk in the Iranian population.
机译:背景:类风湿性关节炎(RA)是具有多因素病因的渐进性和常见的自身免疫疾病。几件研究表明,遗传因素在RA的发病率发挥着重要作用。几种基因组关联研究(GWAS)已将肿瘤坏死因子α诱导蛋白3(TNFAIP3)基因鉴定为候选基因座之一。编码泛素编辑蛋白A20巫婆的TNFAIP3基因限制了B细胞存活并防止自身免疫。以前的研究表明,TNFAIP3基因中的单核苷酸多态性(SNP)与几种自身免疫疾病相关。在本研究中,我们在伊朗人群中评估了TNFAIP3基因中的SNP RS5029937(内肠变异)之间的可能关联。

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