Institute of Clinical Molecular Biology, Christian-Albrechts-University Kiel, Kiel, Germany.
J Invest Dermatol. 2012 Apr;132(4):1133-40. doi: 10.1038/jid.2011.415. Epub 2011 Dec 15.
Psoriatic arthritis (PsA) is a chronic inflammatory musculoskeletal disease affecting up to 30% of psoriasis vulgaris (PsV) cases and approximately 0.25 to 1% of the general population. To identify common susceptibility loci, we performed a meta-analysis of three imputed genome-wide association studies (GWAS) on psoriasis, stratified for PsA. A total of 1,160,703 single-nucleotide polymorphisms (SNPs) were analyzed in the discovery set consisting of 535 PsA cases and 3,432 controls from Germany, the United States, and Canada. We followed up two SNPs in 1,931 PsA cases and 6,785 controls comprising six independent replication panels from Germany, Estonia, the United States, and Canada. In the combined analysis, a genome-wide significant association was detected at 2p16 near the REL locus encoding c-Rel (rs13017599, P=1.18 × 10(-8), odds ratio (OR)=1.27, 95% confidence interval (CI)=1.18-1.35). The rs13017599 polymorphism is known to associate with rheumatoid arthritis (RA), and another SNP near REL (rs702873) was recently implicated in PsV susceptibility. However, conditional analysis indicated that rs13017599, rather than rs702873, accounts for the PsA association at REL. We hypothesize that c-Rel, as a member of the Rel/NF-κB family, is associated with PsA in the context of disease pathways that involve other identified PsA and PsV susceptibility genes including TNIP1, TNFAIP3, and NFκBIA.
银屑病关节炎(PsA)是一种慢性炎症性肌肉骨骼疾病,影响多达 30%的寻常型银屑病(PsV)病例和约 0.25%至 1%的普通人群。为了确定常见的易感基因座,我们对银屑病进行了三项基于全基因组关联研究(GWAS)的荟萃分析,根据是否患有 PsA 进行分层。在包含来自德国、美国和加拿大的 535 例 PsA 病例和 3432 例对照的发现集中,分析了 1160703 个单核苷酸多态性(SNP)。我们在包含来自德国、爱沙尼亚、美国和加拿大的 6785 例对照和 1931 例 PsA 病例的六个独立复制面板中对两个 SNP 进行了随访。在联合分析中,在 REL 基因座附近的 2p16 处检测到与全基因组显著相关,该基因座编码 c-Rel(rs13017599,P=1.18×10(-8),优势比(OR)=1.27,95%置信区间(CI)=1.18-1.35)。rs13017599 多态性与类风湿关节炎(RA)相关,而 REL 附近的另一个 SNP(rs702873)最近与 PsV 易感性有关。然而,条件分析表明,rs13017599 而不是 rs702873 是 REL 与 PsA 相关的原因。我们假设 c-Rel 作为 Rel/NF-κB 家族的成员,与包括 TNIP1、TNFAIP3 和 NFκBIA 在内的其他已确定的 PsA 和 PsV 易感基因相关的疾病途径有关。