首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Comprehensive assessment of rheumatoid arthritis susceptibility loci in a large psoriatic arthritis cohort
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Comprehensive assessment of rheumatoid arthritis susceptibility loci in a large psoriatic arthritis cohort

机译:大型银屑病关节炎队列中类风湿关节炎易感基因座的综合评估

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Objective: A number of rheumatoid arthritis (RA) susceptibility genes have been identified in recent years. Given the overlap in phenotypic expression of synovial joint inflammation between RA and psoriatic arthritis (PsA), the authors explored whether RA susceptibility genes are also associated with PsA. Methods: 56 single nucleotide polymorphisms (SNPs) mapping to 41 genes previously reported as RA susceptibility loci were selected for investigation. PsA was defined as an inflammatory arthritis associated with psoriasis and subjects were recruited from the UK and Ireland. Genotyping was performed using the Sequenom MassArray platform and frequencies compared with data derived from large UK control collections. Results: Significant evidence for association with susceptibility to PsA was found to a SNP mapping to the REL (rs13017599, p trend = 5.2 × 10 4) gene, while nominal evidence for association (p trend 0.05) was found to seven other loci including PLCL2 (rs4535211, p = 1.7 × 10 -3); STAT4 (rs10181656, p = 3.0 × 10 -3) and the AFF3, CD28, CCL21, IL2 and KIF5A loci. Interestingly, three SNPs demonstrated opposite effects to those reported for RA. Conclusions: The REL gene, a key modulator of the NFκB pathway, is associated with PsA but the allele conferring risk to RA is protective in PsA suggesting that there are fundamental differences in the aetiological mechanisms underlying these two types of inflammatory arthritis.
机译:目的:近年来已鉴定出许多类风湿关节炎(RA)易感基因。鉴于RA和银屑病关节炎(PsA)之间滑膜关节发炎的表型表达重叠,作者探讨了RA易感性基因是否也与PsA相关。方法:选择56个单核苷酸多态性(SNPs)映射到先前报道为RA易感基因座的41个基因进行研究。 PsA被定义为与牛皮癣相关的炎性关节炎,受试者从英国和爱尔兰招募。使用Sequenom MassArray平台进行了基因分型,并将频率与来自大型英国对照集合的数据进行了比较。结果:在SNP定位到REL(rs13017599,p趋势= 5.2×10 4)基因的SNP中发现了与PsA易感性相关的重要证据,而与其他七个基因位点相关的名义证据(p趋势<0.05)也被发现。 PLCL2(rs4535211,p = 1.7×10 -3); STAT4(rs10181656,p = 3.0×10 -3)和AFF3,CD28,CCL21,IL2和KIF5A基因座。有趣的是,三个SNP表现出与RA相关的相反作用。结论:REL基因是NFκB通路的关键调节因子,与PsA相关,但赋予RA风险的等位基因在PsA中具有保护作用,这表明这两种类型的炎性关节炎的病因机制存在根本差异。

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