Zheng Yan, Wang Hongluan, Luo Linlin, Liao Liyang, You Luxia, Wang Jun, Li Qiugen
Department of Respiratory Diseases, Jiangxi Province People's Hospital, Nanchang Department of Hepatobiliary Surgery, Shangrao People's Hospital, Shangrao, China.
Medicine (Baltimore). 2018 Jul;97(28):e11380. doi: 10.1097/MD.0000000000011380.
Numerous studies have reported an association between cytotoxic T-lymphocyte associated antigen 4 gene (CTLA4) polymorphism and susceptibility to asthma, in different populations, but the results have been inconsistent. We performed a meta-analysis of 19 published case-control studies to obtain a reasonably accurate estimation of the relationship between CTLA4 polymorphism and asthma.
We searched the Pubmed, EMBASE, Chinese National Knowledge Infrastructure, and Wanfang databases and extracted data from 19 independent, eligible studies. Odds ratios (ORs) with 95% confidence intervals (CIs) and Egger test were separately used to assess the strength of associations and publication bias.
A total of 19 case-control studies involving 4831 cases and 4534 controls were identified. The combined results revealed that there was significant association between the +49A/G polymorphism and asthma (for GG + GA vs. AA: OR = 0.82, 95% CI = 0.70-0.97, P = .02). Stratification by race or age indicated a significant association between the CTLA-4 +49 GA+GG genotype and asthma in Asians (OR = 0.80, 95% CI = 0.68-0.95, P = .01) and children (OR = 0.75, 95% CI = 0.62-0.90, P = .002), but there was no association in whites (OR = 0.94, 95% CI = 0.80-1.10, P = .44) and adults (OR = 0.85, 95% CI = 0.68-1.06, P = .15). Additionally, there was a significant association with atopic asthma under the random-effects model (OR = 0.81, 95% CI = 0.67-0.98, P = .03). In addition, there was no significant association between the -318 C/T polymorphism and asthma risk.
Our meta-analysis results suggested that the +49A/G polymorphism in CTLA-4 was an important risk factor for asthma susceptibility, especially in Asian individuals, children, and atopic patients.
众多研究报告了细胞毒性T淋巴细胞相关抗原4基因(CTLA4)多态性与不同人群哮喘易感性之间的关联,但结果并不一致。我们对19项已发表的病例对照研究进行了荟萃分析,以合理准确地估计CTLA4多态性与哮喘之间的关系。
我们检索了PubMed、EMBASE、中国知网和万方数据库,并从19项独立的合格研究中提取数据。分别使用比值比(OR)及其95%置信区间(CI)和Egger检验来评估关联强度和发表偏倚。
共纳入19项病例对照研究,涉及4831例病例和4534例对照。综合结果显示,+49A/G多态性与哮喘之间存在显著关联(GG + GA与AA相比:OR = 0.82,95% CI = 0.70 - 0.97,P = 0.02)。按种族或年龄分层显示,CTLA - 4 +49 GA + GG基因型与亚洲人(OR = 0.80,95% CI = 0.68 - 0.95,P = 0.01)和儿童(OR = 0.75,95% CI = 0.62 - 0.90,P = 0.002)的哮喘存在显著关联,但在白人(OR = 0.94,95% CI = 0.80 - 1.10,P = 0.44)和成年人(OR = 0.85,95% CI = 0.68 - 1.06,P = 0.15)中无关联。此外,在随机效应模型下,与特应性哮喘存在显著关联(OR = 0.81,95% CI = 0.67 - 0.98,P = 0.03)。另外,-318C/T多态性与哮喘风险之间无显著关联。
我们的荟萃分析结果表明,CTLA - 4中的+49A/G多态性是哮喘易感性的重要危险因素,尤其是在亚洲人、儿童和特应性患者中。