Jeffrey Cheah School of Medicine and Health Sciences, Monash University, Sunway Campus, 46150 Selangor, Malaysia ; Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.
Department of Biomedical Science, Faculty of Medicine, University of Malaya, 50603 Kuala Lumpur, Malaysia.
J Immunol Res. 2014;2014:529167. doi: 10.1155/2014/529167. Epub 2014 Feb 17.
Polymorphisms in genes involved in toll-like receptor/interferon signalling pathways have been reported previously to be associated with SLE in many populations. This study aimed to investigate the role of seven single nucleotide polymorphisms within TNFAIP3, STAT4, and IRF5, which are involved in upstream and downstream pathways of type I interferon production, in SLE in the South East Asian populations. Genotyping of 360 Malaysian SLE patients and 430 normal healthy individuals revealed that minor alleles of STAT4 rs7574865 and rs10168266 were associated with elevated risk of SLE in the Chinese and Malay patients, respectively (P = 0.028, odds ratio (OR) = 1.42; P = 0.035, OR = 1.80, respectively). Polymorphisms in TNFAIP3 and IRF5 did not show significant associations with SLE in any of the ethnicities. Combined analysis of the Malays, Chinese, and Indians for each SNP indicated that STAT4 rs10168266 was significantly associated with the Malaysian SLE as a whole (P = 0.014; OR = 1.435). The meta-analysis of STAT4 rs10168266, which combined the data of other studies and this study, further confirmed its importance as the risk factor for SLE by having pooled OR of 1.559 and P value of <0.001.
先前已有研究报道,涉及 Toll 样受体/干扰素信号通路的基因多态性与许多人群的系统性红斑狼疮(SLE)有关。本研究旨在探讨在 I 型干扰素产生的上下游途径中涉及的 TNFAIP3、STAT4 和 IRF5 基因中的七个单核苷酸多态性在东南亚人群中的 SLE 中的作用。对 360 名马来西亚 SLE 患者和 430 名正常健康个体进行基因分型后发现,STAT4 rs7574865 和 rs10168266 的次要等位基因与中国和马来患者的 SLE 风险升高相关(P=0.028,比值比(OR)=1.42;P=0.035,OR=1.80)。TNFAIP3 和 IRF5 的多态性与任何种族的 SLE 均无显著相关性。对马来人、华人、印度人进行的每个 SNP 的综合分析表明,STAT4 rs10168266 与马来西亚 SLE 整体显著相关(P=0.014;OR=1.435)。对 STAT4 rs10168266 的荟萃分析,将其他研究的数据与本研究相结合,进一步证实了其作为 SLE 风险因素的重要性,合并的比值比(OR)为 1.559,P 值<0.001。