The University of Nottingham, School of Molecular Medical Sciences, University Hospital, Queens Medical Centre, Nottingham, UK.
BMC Med Genet. 2011 Feb 14;12:24. doi: 10.1186/1471-2350-12-24.
Genetic factors are known to contribute to COPD susceptibility and these factors are not fully understood. Conflicting results have been reported for many genetic studies of candidate genes based on their role in the disease. Genome-wide association studies in combination with expression profiling have identified a number of new candidates including IREB2. A meta-analysis has implicated transforming growth factor beta-1 (TGFbeta1) as a contributor to disease susceptibility.
We have examined previously reported associations in both genes in a collection of 1017 white COPD patients and 912 non-diseased smoking controls. Genotype information was obtained for seven SNPs in the IREB2 gene, and for four SNPs in the TGFbeta1 gene. Allele and genotype frequencies were compared between COPD cases and controls, and odds ratios were calculated. The analysis was adjusted for age, sex, smoking and centre, including interactions of age, sex and smoking with centre.
Our data replicate the association of IREB2 SNPs in association with COPD for SNP rs2568494, rs2656069 and rs12593229 with respective adjusted p-values of 0.0018, 0.0039 and 0.0053. No significant associations were identified for TGFbeta1.
These studies have therefore confirmed that the IREB2 locus is a contributor to COPD susceptibility and suggests a new pathway in COPD pathogenesis invoking iron homeostasis.
遗传因素被认为是导致 COPD 易感性的因素,但这些因素尚未完全被理解。基于候选基因在疾病中的作用,许多针对遗传因素的基因研究报告了相互矛盾的结果。全基因组关联研究与表达谱分析已经确定了许多新的候选基因,包括 IREB2。一项荟萃分析表明转化生长因子-β1(TGFβ1)是导致疾病易感性的因素之一。
我们在一组 1017 名白人 COPD 患者和 912 名非患病吸烟对照者中,对这两个基因之前报道的关联进行了检查。IREB2 基因的七个 SNP 和 TGFβ1 基因的四个 SNP 获得了基因型信息。在 COPD 病例和对照组之间比较了等位基因和基因型频率,并计算了比值比。该分析针对年龄、性别、吸烟和中心进行了调整,包括年龄、性别和吸烟与中心的相互作用。
我们的数据复制了 IREB2 基因 SNP 与 COPD 的关联,SNP rs2568494、rs2656069 和 rs12593229 与相应的调整后 p 值分别为 0.0018、0.0039 和 0.0053。TGFβ1 未发现显著关联。
因此,这些研究证实了 IREB2 基因座是 COPD 易感性的一个贡献者,并提示 COPD 发病机制中存在新的铁稳态途径。