Zhang Li, Zhang Tao, Xiang Zhengkai, Lu Shengqiang
Intensive Care Unit Hubei Cancer Hospital Wuhan 430079 China.
Department of Ultrasound Hubei Maternal and Child Health Hospital Wuhan 430070 China.
Mol Genet Genomic Med. 2015 Jul 14;3(6):537-42. doi: 10.1002/mgg3.163. eCollection 2015 Nov.
The present study investigates the association of single-nucleotide polymorphisms (SNPs) on the chloride channel-6 (CLC-6) gene with coronary heart disease (CHD) in China. We carried out a large case-control study among 1193 CHD patients and 1200 unrelated healthy control subjects. Information on the participants' health status was collected through the modified Inter-heart questionnaire. Genomic DNA from peripheral blood samples was analyzed for the genotypes of rs3737964 and rs3737965 SNPs on the CLC-6 gene using Taqman probe-based quantitative real-time PCR (qPCR). We compared the collected data between the case group and the control group by chi-square test and t/nonparametric test. Furthermore, we performed logistic regression to evaluate factors associated with CHD. The frequency of TT genotypes in rs3737964 was significantly higher in CHD patients compared to the control group, with an odds ratio (OR) of 2.32 (95% confidence interval, CI: 1.17-4.06, P = 0.016). The association of CHD with TT genotype was even stronger in smoking population after adjusting for confounders (OR = 3.19, 95% CI: 1.04-9.79, P = 0.043). Multivariate logistic regression showed the CHD risk associated with TT genotype in rs3737964 was particularly among population who were more than 60 years old, smoking, and male (P = 0.023, 0.008 and 0.043, respectively). The present study has revealed that rs3737964 SNP of CLC-6 was associated with CHD. In particular, subjects with TT genotype who were 60-plus years old, with smoking habit or were male were more susceptible to CHD.
本研究调查了中国人群中氯离子通道6(CLC-6)基因单核苷酸多态性(SNP)与冠心病(CHD)的关联。我们对1193例冠心病患者和1200名无血缘关系的健康对照者进行了一项大型病例对照研究。通过改良的心脏调查问卷调查参与者的健康状况信息。使用基于Taqman探针的定量实时聚合酶链反应(qPCR)分析外周血样本的基因组DNA中CLC-6基因rs3737964和rs3737965 SNP的基因型。我们通过卡方检验和t检验/非参数检验比较病例组和对照组收集的数据。此外,我们进行逻辑回归以评估与冠心病相关的因素。与对照组相比,冠心病患者中rs3737964的TT基因型频率显著更高,优势比(OR)为2.32(95%置信区间,CI:1.17 - 4.06,P = 0.016)。在调整混杂因素后,吸烟人群中冠心病与TT基因型的关联更强(OR = 3.19,95% CI:1.04 - 9.79, P = 0.043)。多变量逻辑回归显示,rs3737964中与TT基因型相关的冠心病风险在60岁以上、吸烟和男性人群中尤为突出(P分别为0.023、0.008和0.043)。本研究表明,CLC-6基因的rs3737964 SNP与冠心病有关。特别是,60岁以上、有吸烟习惯或男性的TT基因型受试者更容易患冠心病。