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一个与中国汉族人群系统性红斑狼疮相关的新的易感基因位点。

One novel susceptibility locus associate with systemic lupus erythematosus in Chinese Han population.

机构信息

Department of Dermatology, Institute of Dermatology, the First Affiliated Hospital, Anhui Medical University, 81 Meishan Road, Hefei 230032, Anhui, People's Republic of China.

出版信息

Rheumatol Int. 2013 Aug;33(8):2079-83. doi: 10.1007/s00296-013-2697-0. Epub 2013 Feb 14.

DOI:10.1007/s00296-013-2697-0
PMID:23408151
Abstract

The aim of the study is to explore additional susceptibility factors for systemic lupus erythematosus (SLE) in Chinese Hans. Based on our previous GWAS of SLE, we performed a multistage replication study involving 3,152 cases and 7,050 controls from China to identify additional susceptibility loci for SLE by using the Sequenom MassArray system. All Chinese Han samples used in this study were obtained from doctors through collaboration with multiple hospitals in two geographic regions (central and southern China). Single-marker association analyses were performed using logistic regression with gender as a covariate in each case-control cohort. The joint analysis of all combined samples was performed using logistic regression with gender and sample cohorts as covariates. The significant association evidence for rs906868 (OR = 1.14, 95% CI 1.08-1.20, P combined = 7.71 × 10(-10)) and rs7579944 (OR = 1.13, 95% CI 1.07-1.19, P combined = 5.55 × 10(-9)) was observed, which located at 2p23.1. In this region, limb bud and heart development homolog (LBH) was the only gene indicated, suggesting LBH might be a susceptibility gene for SLE, although its function was still unknown. The results indicated that the SNP rs7579944, rs906868 at 2p23.1 showed significant association with SLE. The genes LBH which located in this loci might be the predisposing genes of SLE.

摘要

本研究旨在探讨中国汉族人群系统性红斑狼疮(SLE)的其他易感因素。基于我们之前对 SLE 的 GWAS 研究结果,我们在中国进行了一项多阶段的复制研究,共纳入了 3152 例病例和 7050 例对照,使用 Sequenom MassArray 系统,通过全基因组关联分析(GWAS)寻找 SLE 的其他易感基因座。本研究中使用的所有中国汉族样本均通过与中国两个地理区域(中部和南部)的多家医院合作,从医生处获得。在每个病例对照队列中,使用逻辑回归分析,并以性别为协变量进行单标记关联分析。在所有联合样本的联合分析中,使用逻辑回归分析,并以性别和样本队列为协变量。rs906868(OR=1.14,95%CI 1.08-1.20,P 联合=7.71×10(-10))和 rs7579944(OR=1.13,95%CI 1.07-1.19,P 联合=5.55×10(-9))的显著关联证据被观察到,这些 SNP 位于 2p23.1 上。在这个区域中,肢体芽和心脏发育同源物(LBH)是唯一被指出的基因,表明 LBH 可能是 SLE 的易感基因,尽管其功能尚不清楚。结果表明,位于 2p23.1 上的 SNP rs7579944、rs906868 与 SLE 显著相关。位于该基因座上的 LBH 基因可能是 SLE 的易感基因。

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