Department of Neurology, Affiliated Hospital of North Sichuan Medical College, Nanchong 637000, People's Republic of China.
Mol Biol Rep. 2012 Feb;39(2):1371-6. doi: 10.1007/s11033-011-0871-6. Epub 2011 May 25.
Some studies have shown that IL-18 was associated with aetiology and progression of asthma. However, the association between single-nucleotide polymorphisms -607C/A (rs1946518) and -137G/C (rs187238) located in the IL-18 gene promoter and asthma risk was still controversial and ambiguous. To derive a more precise effect on the association between these polymorphisms and asthma risk, we performed a meta-analysis based on the currently available evidence of the literature. A total of 5 studies with 1411 cases and 1525 controls for -607C/A polymorphism and 5 studies with 1883 cases and 6645 controls for -137G/C polymorphism were identified to perform a meta-analysis, up to October 2010. Summary ORs and corresponding 95% CIs for IL-18 polymorphisms and asthma were estimated using fixed- and random-effects models when appropriate. Heterogeneity and publication bias were evaluated. We found that individuals carrying AC/CC genotype of -607C/A polymorphism were associated with an increased asthma risk in recessive model (OR = 1.278; 95% CI, 1.073-1.522). However, no significant association was observed between -137G/C polymorphism and asthma risk under different contrast models. There was no evidence of publication bias. The present meta-analysis suggested that IL-18 -607C/A polymorphism in promoter region was associated with asthma risk.
一些研究表明白细胞介素-18(IL-18)与哮喘的病因和进展有关。然而,位于 IL-18 基因启动子中的单核苷酸多态性 -607C/A(rs1946518)和-137G/C(rs187238)与哮喘风险之间的关联仍然存在争议和不明确。为了更准确地评估这些多态性与哮喘风险之间的关联,我们基于现有文献证据进行了荟萃分析。截至 2010 年 10 月,共确定了 5 项研究,其中包括 1411 例病例和 1525 例对照用于 -607C/A 多态性,以及 5 项研究,其中包括 1883 例病例和 6645 例对照用于 -137G/C 多态性,以进行荟萃分析。使用固定效应和随机效应模型适当估计 IL-18 多态性和哮喘的汇总 OR 及其相应的 95%置信区间。评估了异质性和发表偏倚。我们发现,在隐性模型中,携带 -607C/A 多态性的 AC/CC 基因型的个体患哮喘的风险增加(OR = 1.278;95%CI,1.073-1.522)。然而,在不同的对比模型下,-137G/C 多态性与哮喘风险之间没有观察到显著的关联。没有发现发表偏倚的证据。本荟萃分析表明,启动子区域的 IL-18-607C/A 多态性与哮喘风险相关。