Wang S-H, Xu F, Dang H-X, Yang L
Pediatric Intensive Care Unit, Children's Hospital, Chongqing Medical University, Chongqing, China.
Genet Mol Res. 2013 Jun 11;12(2):1829-33. doi: 10.4238/2013.January.4.1.
Identifying genetic determinants for lung function is important in providing insight into the pathophysiology of asthma. The Wnt signal pathway plays a role in lung development and in asthma pathogenesis. However, whether genetic polymorphisms of Wnt signal pathway are associated with lung function in asthma patients remain unclear. We genotyped 2 single nucleotide polymorphisms (SNPs, rs2929973 and rs6581612) involved in the Wnt signal pathway in a cohort of 560 Chinese Han asthmatic children. Associations between each SNP and lung function, in a baseline exam, were tested using multiple linear regression models. We found that rs2929973 of the WISP1 gene was significantly associated with forced expiratory volume in 1 s (FEV1), with the G allele conferring significantly lower FEV1 values. However, the rs6581612 SNP of the WIF1 gene was not associated with differences in FEV1 values. We conclude that genetic variants in Wnt are associated with lung function and suggest that Wnt participates in inflammatory pathways that have an impact on the level of lung function.
确定肺功能的遗传决定因素对于深入了解哮喘的病理生理学至关重要。Wnt信号通路在肺发育和哮喘发病机制中发挥作用。然而,Wnt信号通路的基因多态性是否与哮喘患者的肺功能相关仍不清楚。我们对560名中国汉族哮喘儿童队列中涉及Wnt信号通路的2个单核苷酸多态性(SNP,rs2929973和rs6581612)进行了基因分型。在基线检查中,使用多元线性回归模型测试每个SNP与肺功能之间的关联。我们发现WISP1基因的rs2929973与第1秒用力呼气量(FEV1)显著相关,G等位基因导致FEV1值显著降低。然而,WIF1基因的rs6581612 SNP与FEV1值的差异无关。我们得出结论,Wnt中的基因变异与肺功能相关,并表明Wnt参与了对肺功能水平有影响的炎症途径。