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首页> 外文期刊>Gene: An International Journal Focusing on Gene Cloning and Gene Structure and Function >Susceptibility of multiple polymorphisms in ADIPOQ, ADIPOR1 and ADIPOR2 genes to myocardial infarction in Han Chinese
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Susceptibility of multiple polymorphisms in ADIPOQ, ADIPOR1 and ADIPOR2 genes to myocardial infarction in Han Chinese

机译:在汉语中脂肪症,Adipor1和Adipor2基因对脂肪,adipor1和adipor2基因的多态性易感性

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We aimed to investigate the association of 12 extensively studied polymorphisms in adiponectin (ADIPOQ), adiponectin receptor-1 (ADIPOR1) and adiponectin receptor-2 (ADIPOR2) genes with myocardial infarction in Han Chinese. This is a hospital-based, cross-sectional, case-control study, including 717 myocardial infarction patients and 612 controls. Myocardial infarction was confirmed through electrocardiogram/anatomopathological examinations. All polymorphisms met the Hardy-Weinberg equilibrium (p 0.05). The genotype/allele counts of ADIPOQ gene rs2241766 (p = 0.001/0.003) and ADIPOR2 gene rs10773989 (p 0.001/ = 0.008) differed significantly between patients and controls. Under the recessive model, rs2241766 (odds ratio [OR] = 4.16, 95% confidence interval [Cl]: 1.83-9.49, p = 0.001) and rs10773989 (OR = 8.40, 95% CI: 2.54-27.8, p 0.001) were associated with the significantly increased risk of myocardial infarction. Haplotype analysis revealed none or marginal significance, and there was no likelihood of genetic interaction as indicated by multifactor dimensionality reduction (MDR). Logistic regression analysis indicated that age, total cholesterol, hypertension, rs2241766, rs1342387, rs10773989 and rs1044471 were significant contributors, and a nomo-gram based on these contributors exhibited a good predictive utility (C-index: 0.795, p 0.001). Our findings demonstrate that two polymorphisms, rs2241766 in ADIPOQ gene and rs10773989 in ADIPOR2 gene, especially under the recessive model of inheritance, played independent leading roles in susceptibility to myocardial infarction in Han Chinese.
机译:我们的旨在调查12在汉语中患有心肌梗死的脂联素(AdipoQ),脂联素受体-1(Adipor1)和脂联素受体-2(Adipor2)基因中的12种受到的多态性的关联。这是一种基于医院,横截面,病例对照研究,包括717名心肌梗死患者和612例对照。通过心电图/解剖病理学检查证实了心肌梗死。所有多态性都符合Hardy-Weinberg平衡(P&GT; 0.05)。患者和对照之间的adipoQ基因RS2241766(P = 0.001 / 0.003)和Adipor2 Gene rs10773989(P <0.001 / = 0.008)的基因型/等位基因计数显着不同。在隐性模型下,RS2241766(差距[或] = 4.16,95%置信区间[Cl]:1.83-9.49,P = 0.001)和Rs10773989(或= 8.40,95%CI:2.54-27.8,P <0.001 )与心肌梗死的风险显着增加。单倍型分析显示无或边际意义,并且遗传相互作用的可能性,如多重吸引力的维度减少(MDR)所示。逻辑回归分析表明,年龄,总胆固醇,高血压,RS2241766,RS1342387,RS10773989和RS104471是重要贡献者,并且基于这些贡献者的Nomo-Gram表现出良好的预测效用(C折射率:0.795,P <0.001)。我们的研究结果表明,AdipoOQ基因的两种多态性,RS2241766和adipor2基因的Rs10773989,特别是在遗传的隐性模型下,对汉族人心肌梗死的易感性发挥了独立的主导作用。

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