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全基因组关联研究鉴定出 TNFSF15 和 POU2AF1 是日本人群原发性胆汁性胆管炎的易感基因位点。

Genome-wide association study identifies TNFSF15 and POU2AF1 as susceptibility loci for primary biliary cirrhosis in the Japanese population.

机构信息

Clinical Research Center, National Hospital Organization (NHO) Nagasaki Medical Center, and Department of Hepatology, Nagasaki University Graduate School of Biomedical Sciences, Omura, Nagasaki 856-8562, Japan.

出版信息

Am J Hum Genet. 2012 Oct 5;91(4):721-8. doi: 10.1016/j.ajhg.2012.08.010. Epub 2012 Sep 20.

Abstract

For the identification of susceptibility loci for primary biliary cirrhosis (PBC), a genome-wide association study (GWAS) was performed in 963 Japanese individuals (487 PBC cases and 476 healthy controls) and in a subsequent replication study that included 1,402 other Japanese individuals (787 cases and 615 controls). In addition to the most significant susceptibility region, human leukocyte antigen (HLA), we identified two significant susceptibility loci, TNFSF15 (rs4979462) and POU2AF1 (rs4938534) (combined odds ratio [OR] = 1.56, p = 2.84 × 10(-14) for rs4979462, and combined OR = 1.39, p = 2.38 × 10(-8) for rs4938534). Among 21 non-HLA susceptibility loci for PBC identified in GWASs of individuals of European descent, three loci (IL7R, IKZF3, and CD80) showed significant associations (combined p = 3.66 × 10(-8), 3.66 × 10(-9), and 3.04 × 10(-9), respectively) and STAT4 and NFKB1 loci showed suggestive association with PBC (combined p = 1.11 × 10(-6) and 1.42 × 10(-7), respectively) in the Japanese population. These observations indicated the existence of ethnic differences in genetic susceptibility loci to PBC and the importance of TNF signaling and B cell differentiation for the development of PBC in individuals of European descent and Japanese individuals.

摘要

为了鉴定原发性胆汁性肝硬化(PBC)的易感基因座,我们对 963 名日本个体(487 名 PBC 病例和 476 名健康对照)进行了全基因组关联研究(GWAS),并在随后的一项包括 1402 名其他日本个体(787 名病例和 615 名对照)的复制研究中进行了验证。除了最显著的易感区域 HLA 之外,我们还鉴定出了两个显著的易感基因座,TNF 配体超家族成员 15(rs4979462)和 POU 结构域转录因子 2 相关因子 1(rs4938534)(联合优势比[OR] = 1.56,p = 2.84×10(-14),rs4979462;联合 OR = 1.39,p = 2.38×10(-8),rs4938534)。在欧洲裔个体的 PBC GWAS 中鉴定出的 21 个非 HLA 易感基因座中,三个基因座(IL7R、IKZF3 和 CD80)显示出显著关联(联合 p = 3.66×10(-8),3.66×10(-9),和 3.04×10(-9),分别),STAT4 和 NFKB1 基因座与 PBC 呈显著关联(联合 p = 1.11×10(-6)和 1.42×10(-7),分别)在日本人群中。这些观察结果表明,PBC 的遗传易感基因座存在种族差异,TNF 信号和 B 细胞分化在欧洲裔和日本个体中对 PBC 的发生发展具有重要意义。

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