Liang Jingyao, Zhang Sanquan, Luo Quan, Li Wei, Tian Xin, Zhang Fang, Zhao Tian, Chen Xiaoxiao, Zhang Xibao
Institute of Dermatology, Guangzhou Medical University, Guangzhou 510095, PR China; Department of Dermatology, Guangzhou Institute of Dermatology, Guangzhou 510095, PR China.
Institute of Dermatology, Guangzhou Medical University, Guangzhou 510095, PR China.
Gene. 2015 Sep 1;568(2):196-202. doi: 10.1016/j.gene.2015.05.051. Epub 2015 May 24.
Cytotoxic T-lymphocyte antigen-4 (CTLA-4) is a critical negative regulator of T-cell activation and proliferation. Several studies have assessed the association between CTLA-4+49A/G polymorphism and psoriasis and vitiligo, but the results are inconsistent.
This study was conducted to examine the association between CTLA-4+49A/G polymorphism and psoriasis and vitiligo susceptibility.
The PubMed, Embase, and China National Knowledge Infrastructure (CNKI) databases were searched according to predefined criteria for all relevant studies published prior to July 3, 2014. Odds ratios (ORs) with 95% confidence intervals (CIs), and heterogeneity and publication bias tests were performed to estimate the strength of the association.
Fourteen studies comprising six on psoriasis (700 cases, 781 controls) and eight on vitiligo (1514 cases, 2049 controls) were included. Overall, no significant association was detected between CTLA-4+49A/G polymorphism and psoriasis. There was still no significant relationship when the studies were limited to ethnicity (Asian and Caucasian), HWE or heterogeneity, except the limitation to heterogeneity in the dominant (OR=0.69, 95% CI=0.51-0.93, I(2)=0.0%) and additive (OR=0.69, 95% CI=0.48-0.98, I(2)=0.0%) models, and the limitation to both heterogeneity and HWE in the dominant model (OR=0.68, 95% CI=0.48-0.98, I(2)=0.0%). Both overall and subgroup analyses based on ethnicity, genotype frequencies, and heterogeneity also failed to demonstrate an association between CTLA-4+49A/G polymorphism and vitiligo.
CTLA-4+49A/G polymorphism may not contribute to psoriasis and vitiligo susceptibility, but further well-designed studies with large sample size are warranted to confirm this conclusion.
细胞毒性T淋巴细胞抗原4(CTLA-4)是T细胞活化和增殖的关键负调节因子。多项研究评估了CTLA-4 +49A/G多态性与银屑病和白癜风之间的关联,但结果并不一致。
本研究旨在探讨CTLA-4 +49A/G多态性与银屑病和白癜风易感性之间的关联。
根据预定义标准检索了PubMed、Embase和中国国家知识基础设施(CNKI)数据库,以获取2014年7月3日前发表的所有相关研究。计算比值比(OR)及其95%置信区间(CI),并进行异质性和发表偏倚检验以评估关联强度。
纳入了14项研究,其中6项关于银屑病(700例病例,781例对照),8项关于白癜风(1514例病例,2049例对照)。总体而言,未检测到CTLA-4 +49A/G多态性与银屑病之间存在显著关联。当研究限于种族(亚洲人和白种人)、哈迪-温伯格平衡(HWE)或异质性时,仍未发现显著关系,但在显性模型(OR=0.69,95%CI=0.51-0.93,I²=0.0%)和加性模型(OR=0.69,95%CI=0.48-0.98,I²=0.0%)中限于异质性时,以及在显性模型中限于异质性和HWE时(OR=0.68,95%CI=0.48-0.98,I²=0.0%)除外。基于种族、基因型频率和异质性的总体及亚组分析均未显示CTLA-4 +49A/G多态性与白癜风之间存在关联。
CTLA-4 +49A/G多态性可能与银屑病和白癜风易感性无关,但需要进一步开展设计良好的大样本研究以证实这一结论。