Kang Sang Wook, Kim Su Kang, Han Young Rok, Hong DongWhan, Chon Jinmann, Chung Joo-Ho, Hong Seoung-Jin, Park Min-Su, Ban Ju Yeon
1 Department of Dental Pharmacology, School of Dentistry, Dankook University, Cheonan, Republic of Korea.
2 Department of Biomedical Laboratory Science, Catholic Kwandong University, Gangneung, Republic of Korea.
Genet Test Mol Biomarkers. 2019 Jun;23(6):363-372. doi: 10.1089/gtmb.2018.0238.
The relationship between the promoter polymorphism (-308G/A) of the tumor necrosis factor-alpha () gene and the susceptibility to asthma has been tested in several studies. However, the results have been inconsistent. Therefore, we performed an updated meta-analysis to evaluate the relationship between this promoter polymorphism of the gene and the risk of asthma. Fifty case-control studies were included in this meta-analysis which provided 17,937 controls and 9961 asthma patients. The pooled -value, odds ratio (OR), and 95% confidence interval (95% CI) were used to investigate the strength of the association of this polymorphism of the gene with the risk of asthma. The meta-analysis was carried out by Comprehensive Meta-Analysis software. The results of our meta-analysis revealed that the polymorphism (-308, G/A) was strongly associated with the risk of asthma ( < 0.05 in the allelic, dominant, and recessive models, respectively). In further analyses, based on age group and ethnicity, we observed this association for all subpopulations examined ( < 0.05 in allelic, dominant, and recessive models, respectively). This large-scale meta-analysis supports a strong association between the gene promoter polymorphism (-308G/A) and the development to asthma in both children and adults.
肿瘤坏死因子-α(TNF-α)基因启动子多态性(-308G/A)与哮喘易感性之间的关系已在多项研究中进行了检测。然而,结果并不一致。因此,我们进行了一项更新的荟萃分析,以评估该基因启动子多态性与哮喘风险之间的关系。本荟萃分析纳入了50项病例对照研究,共提供了17937名对照和9961名哮喘患者。采用合并P值、比值比(OR)和95%置信区间(95%CI)来研究该基因多态性与哮喘风险的关联强度。荟萃分析通过综合荟萃分析软件进行。我们的荟萃分析结果显示,TNF-α多态性(-308,G/A)与哮喘风险密切相关(等位基因、显性和隐性模型中的P值均<0.05)。在进一步基于年龄组和种族的分析中,我们在所检查的所有亚组中均观察到了这种关联(等位基因、显性和隐性模型中的P值均<0.05)。这项大规模荟萃分析支持TNF-α基因启动子多态性(-308G/A)与儿童和成人哮喘发病之间存在密切关联。