Yang W, Ng P, Zhao M, Hirankarn N, Lau C S, Mok C C, Chan T M, Wong R W S, Lee K W, Mok M Y, Wong S N, Avihingsanon Y, Lee T L, Ho M H K, Lee P P W, Wong W H S, Lau Y L
Department of Paediatrics and Adolescent Medicine, Queen Mary Hospital, Li Ka Shing Faculty of Medicine, The University of Hong Kong, Hong Kong, China.
Genes Immun. 2009 Apr;10(3):219-26. doi: 10.1038/gene.2009.1. Epub 2009 Feb 19.
In this study, we compared the association of several newly discovered susceptibility genes for systemic lupus erythematosus (SLE) between populations of European origin and two Asian populations. Using 910 SLE patients and 1440 healthy controls from Chinese living in Hong Kong, and 278 SLE patients and 383 controls in Thailand, we studied association of STAT4, BLK and PXK with the disease. Our data confirmed association of STAT4 (rs7574865, odds ratio (OR) =1.71, P=3.55 x 10(-23)) and BLK (rs13277113, OR=0.77, P=1.34 x 10(-5)) with SLE. It was showed that rs7574865 of STAT4 is also linked to hematologic disorders and potentially some other subphenotypes of the disease. More than one genetic variant in STAT4 were found to be associated with the disease independently in our populations (rs7601754, OR=0.59, P=1.39 x 10(-9), and P=0.00034 when controlling the effect of rs7574865). With the same set of samples, however, our study did not detect any significant disease association for PXK, a risk factor for populations of European origin (rs6445975, joint P=0.36, OR=1.06, 95% confidence interval: 0.93-1.21). Our study indicates that some of the susceptibility genes for this disease may be population specific.
在本研究中,我们比较了欧洲裔人群与两个亚洲人群中几种新发现的系统性红斑狼疮(SLE)易感基因的关联。我们使用了来自中国香港的910例SLE患者和1440名健康对照,以及泰国的278例SLE患者和383名对照,研究了STAT4、BLK和PXK与该疾病的关联。我们的数据证实了STAT4(rs7574865,优势比(OR)=1.71,P=3.55×10⁻²³)和BLK(rs13277113,OR=0.77,P=1.34×10⁻⁵)与SLE相关。结果显示,STAT4的rs7574865也与血液系统疾病以及该疾病的一些其他潜在亚表型有关。在我们的人群中,发现STAT4中有不止一个基因变异与该疾病独立相关(rs7601754,OR=0.59,P=1.39×10⁻⁹,在控制rs7574865的效应时P=0.00034)。然而,使用同一组样本,我们的研究未检测到PXK(欧洲裔人群的一个风险因素)与疾病有任何显著关联(rs6445975,联合P=0.36,OR=1.06,95%置信区间:
0.93 - 1.21)。我们的研究表明,该疾病的一些易感基因可能具有人群特异性。