Department of Respiratory Medicine, West China Hospital, Sichuan University, Chengdu, China.
Respirology. 2014 Apr;19(3):312-20. doi: 10.1111/resp.12235. Epub 2014 Jan 14.
A number of polymorphisms in a disintegrin and metalloprotease 33 (ADAM33) gene have been implicated in susceptibility to chronic obstructive pulmonary disease (COPD). However, results to date have been inconclusive. We conducted meta-analyses to investigate the associations between multiple polymorphisms in ADAM33 gene and COPD susceptibility. PubMed, Embase and Chinese databases (Wanfang and China National Knowledge Infrastructure) were searched for eligible case-control studies. We extracted data and used meta-analysis to calculate pooled odds ratios with 95% confidence intervals to evaluate the strength of associations. Twelve studies containing six ADAM33 polymorphisms (F+1, S1, S2, T1, V4 and Q-1) were identified, which involved 2630 cases and 4376 controls. ADAM33 S1 polymorphism showed stable and significant associations with COPD risks among the Chinese and smoking populations, and Q-1 polymorphism showed stable and significant associations with COPD risks among the overall populations. In subgroup analyses, T1 and Q-1 polymorphisms were significantly associated with COPD risks among the Chinese and smoking populations, and among the Chinese, Caucasians and smoking populations, respectively. However, none of the significant results was stable in sensitivity analyses. With respect to F+1, S2 or V4 polymorphism, there was no evidence of any significant association with COPD risks in either the overall or the subgroup analysis. The results of this meta-analysis indicate that ADAM33 S1 polymorphism is a risk factor for COPD among the Chinese and smoking populations, and that Q-1 polymorphism is a risk factor for COPD among the overall populations.
多种解整合素金属蛋白酶 33(ADAM33)基因的多态性与慢性阻塞性肺疾病(COPD)易感性有关。然而,迄今为止的结果尚无定论。我们进行了荟萃分析,以研究 ADAM33 基因多个多态性与 COPD 易感性之间的关联。检索了 PubMed、Embase 和中国数据库(万方和中国国家知识基础设施)以获取合格的病例对照研究。我们提取数据并使用荟萃分析计算合并优势比及其 95%置信区间,以评估关联的强度。确定了包含六个 ADAM33 多态性(F+1、S1、S2、T1、V4 和 Q-1)的 12 项研究,这些研究涉及 2630 例病例和 4376 例对照。ADAM33 S1 多态性在中国人群和吸烟人群中与 COPD 风险之间存在稳定且显著的关联,而 Q-1 多态性在总体人群中与 COPD 风险之间存在稳定且显著的关联。在亚组分析中,T1 和 Q-1 多态性与中国人群和吸烟人群以及中国人群、白种人群和吸烟人群中的 COPD 风险显著相关。但是,在敏感性分析中,没有一个显著结果是稳定的。关于 F+1、S2 或 V4 多态性,在总体或亚组分析中均没有证据表明与 COPD 风险有任何显著关联。荟萃分析的结果表明,ADAM33 S1 多态性是中国人群和吸烟人群中 COPD 的危险因素,而 Q-1 多态性是总体人群中 COPD 的危险因素。