Zhang Zhaoqiang, Wang Lei, Sun Xiao, Zhang Li, Lu Lianyuan
Department of Physiology, Basic Medical College of Taishan Medical University, Taian, China.
Department of Nephrology, Taian Central Hospital, Taian, China.
J Neurol Sci. 2016 Apr 15;363:107-13. doi: 10.1016/j.jns.2016.02.049. Epub 2016 Feb 22.
Previous studies have suggested a role for interleukin-4 (IL4) and its receptor (IL4R) gene in susceptibility to multiple sclerosis (MS), but the results remain controversial and under-powered.
To investigate the contradictory results, we performed a meta-analysis to assess the possible association between polymorphisms of the IL4 rs2243250 (C/T), variable number of tandem repeat (VNTR) polymorphism in intron-3 (I3(709)VNTR), IL4R rs1801275 (T/C) and MS in Caucasian populations.
A comprehensive search was conducted to identify all case-control or cohort design studies. The fixed or random effect pooled measure was selected based on the homogeneity test among studies that was evaluated with I(2). Publication bias was estimated using the Begg's and Egger's test.
A total of ten studies were included in the meta-analysis. The crude odds ratios (ORs) with 95% confidence intervals (95% CI) were calculated to evaluate the association. Overall, after excluding articles deviating from Hardy-Weinberg equilibrium in controls and sensitive analysis, the meta-analysis showed a significant association between polymorphism of IL4 rs2243250 and MS susceptibility in allele model (OR=1.209, 95% CI=1.022-1.429, P=0.026) and dominant model (OR =1.225, 95% CI=1.013-1.480, P=0.036). However, no significant association was found between polymorphisms of IL4 I3(709)*VNTR, IL4R rs1801275 and MS susceptibility, respectively.
The meta-analysis indicates that the T allele, CT and TT genotype of polymorphism of IL4 rs2243250 (C/T) may reduce the risk of MS in Caucasian populations, while polymorphisms of IL4 I3(709)*VNTR and IL4R rs1801275 may not associated with risk of MS in Caucasian populations.
既往研究提示白细胞介素-4(IL4)及其受体(IL4R)基因在多发性硬化症(MS)易感性中起一定作用,但结果仍存在争议且样本量不足。
为探究这些相互矛盾的结果,我们进行了一项荟萃分析,以评估白种人群中IL4 rs2243250(C/T)多态性、内含子3可变数目串联重复序列(VNTR)多态性(I3(709)VNTR)、IL4R rs1801275(T/C)与MS之间的可能关联。
进行全面检索以识别所有病例对照或队列设计研究。根据用I(2)评估的研究间同质性检验选择固定效应或随机效应合并测量方法。使用Begg检验和Egger检验估计发表偏倚。
荟萃分析共纳入10项研究。计算了95%置信区间(95%CI)的粗比值比(OR)以评估关联。总体而言,在排除对照组偏离哈迪-温伯格平衡的文章并进行敏感性分析后,荟萃分析显示IL4 rs2243250多态性在等位基因模型(OR=1.209,95%CI=1.022-1.429,P=0.026)和显性模型(OR =1.225,95%CI=1.013-1.480,P=0.036)中与MS易感性之间存在显著关联。然而,分别未发现IL4 I3(709)*VNTR、IL4R rs1801275多态性与MS易感性之间存在显著关联。
荟萃分析表明,IL4 rs2243250(C/T)多态性的T等位基因、CT和TT基因型可能降低白种人群患MS的风险,而IL4 I3(709)*VNTR和IL4R rs1801275多态性可能与白种人群患MS的风险无关。