Zhang Guimin, Zhang Di, Shi Wenjie, Sun Peiyong, Lin Peng
Department of Otolaryngology-Head and Neck Surgery, Tianjin First Center Hospital, Tianjin, People's Republic of China.
Ann Hum Genet. 2017 Nov;81(6):284-291. doi: 10.1111/ahg.12205. Epub 2017 Jul 25.
Polymorphisms of several genes were reported to be associated with the risk of allergic rhinitis. Here, we first conducted a meta-analysis to evaluate the potential genetic association between the polymorphisms of the FOXP3 (Forkhead Box P3) gene and the susceptibility to allergic rhinitis. A total of 2671 relevant articles were initially retrieved from the databases of PubMed, Web of Science, Embase, WANFANG/CNKI and Scopus, and six eligible case-control studies were finally enrolled in our meta-analysis, according to our strict inclusion/exclusion criteria. Based on the extracted data, Mantel-Haenszel statistic, Cochrane's Q statistic, I test, subgroup meta-analysis, Begg's test, Egger's test and sensitivity analysis were performed via Stata/SE 12.0 software. The results of the Mantel-Haenszel statistic regarding rs3761548 showed that no significant difference was observed in the allergic rhinitis case and population-based control group under the genetic models of A versus C, AA versus CC, CA+AA versus CC, AA versus CC+CA and carrier A versus C (all P-value of Association Test, P > 0.05), apart from CA versus CC (P = 0.020). The similar results were obtained in the subgroup analysis of Asian. In addition, we did not obtain the positive result in the meta-analysis of rs2232365 (all P > 0.05). We also excluded the presence of large publication bias through Begg's test and Egger's test, and we confirmed the stability of data by sensitivity analysis. In summary, no significant association between rs3761548, rs2232365 polymorphisms of the FOXP3 gene, and an increased susceptibility to allergic rhinitis was identified based on the published data; however, this conclusion should be confirmed by more studies with increased sample sizes.
据报道,多个基因的多态性与过敏性鼻炎的风险相关。在此,我们首先进行了一项荟萃分析,以评估FOXP3(叉头框P3)基因多态性与过敏性鼻炎易感性之间的潜在遗传关联。最初从PubMed、Web of Science、Embase、万方/知网和Scopus数据库中检索到总共2671篇相关文章,根据我们严格的纳入/排除标准,最终有六项符合条件的病例对照研究纳入我们的荟萃分析。基于提取的数据,通过Stata/SE 12.0软件进行Mantel-Haenszel统计、Cochrane's Q统计、I检验、亚组荟萃分析、Begg检验、Egger检验和敏感性分析。关于rs3761548的Mantel-Haenszel统计结果显示,在A与C、AA与CC、CA+AA与CC、AA与CC+CA以及携带A与C的遗传模型下,过敏性鼻炎病例组和基于人群的对照组之间未观察到显著差异(所有关联检验的P值,P>0.05),除了CA与CC(P = 0.020)。在亚洲人的亚组分析中也得到了类似结果。此外,我们在rs2232365的荟萃分析中未获得阳性结果(所有P>0.05)。我们还通过Begg检验和Egger检验排除了存在大的发表偏倚,并通过敏感性分析证实了数据的稳定性。总之,根据已发表的数据,未发现FOXP3基因的rs3761548、rs2232365多态性与过敏性鼻炎易感性增加之间存在显著关联;然而,这一结论应通过更多样本量增加的研究来证实。