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成纤维细胞生长因子受体 4 多态性与冠心病易感性。

Fibroblast growth factor receptor 4 polymorphisms and susceptibility to coronary artery disease.

机构信息

Department of Cardiology, Shanghai East Hospital, Tongji University, Shanghai, China.

出版信息

DNA Cell Biol. 2012 Jun;31(6):1064-9. doi: 10.1089/dna.2011.1552. Epub 2012 Feb 7.

Abstract

Fibroblast growth factors (FGFs) and their receptors (FGFRs) play crucial roles in vascular smooth muscle cell proliferation and atherosclerosis and, therefore, may potentially affect the development of coronary artery disease (CAD). FGFR4 rs351855 (Gly388Arg) polymorphism has shown to be a risk factor for many diseases. The aim of this study was to investigate the association between FGFR4 polymorphisms and the susceptibility to CAD in the Chinese population. Two polymorphisms, rs351855 (Gly388Arg) and rs641101, were detected by polymerase chain reaction-restriction fragment length polymorphism and direct sequencing in 687 CAD cases and 732 age-matched controls. Data were analyzed using the chi-square test. Results showed that frequencies of GA genotype, AA genotype, and A allele in rs351855 (Gly388Arg) polymorphism were significantly lower in CAD patients than in controls (odds ratio (OR)=0.78, 95% confidence intervals (CIs): 0.62-0.98, p=0.034; OR=0.58, 95% CI: 0.42-0.80, p=0.001; and OR=0.77, 95% CI: 0.66-0.90, p=0.001, respectively). The rs641101 polymorphism did not show any correlation with CAD. Haplotype analysis revealed that rs351855 and rs641101 AG haplotype also had lower frequency in CAD patients (OR=0.79, 95% CI: 0.67-0.92, p=0.002). Our data suggested that the FGFR4 rs351855 (Gly388Arg) polymorphism and AG haplotype (rs351855 and rs641101) could act as protective factors against CAD in the Chinese population and indicated that a single gene polymorphism could have diverse functions in different diseases.

摘要

成纤维细胞生长因子 (FGFs)及其受体 (FGFRs) 在血管平滑肌细胞增殖和动脉粥样硬化中发挥着关键作用,因此可能会影响冠心病 (CAD) 的发展。FGFR4 rs351855 (Gly388Arg) 多态性已被证明是许多疾病的危险因素。本研究旨在探讨 FGFR4 多态性与中国人群 CAD 易感性之间的关系。通过聚合酶链反应-限制性片段长度多态性和直接测序检测了 687 例 CAD 病例和 732 例年龄匹配对照中的两种多态性 rs351855 (Gly388Arg) 和 rs641101。数据采用卡方检验进行分析。结果表明,rs351855 (Gly388Arg) 多态性中 GA 基因型、AA 基因型和 A 等位基因的频率在 CAD 患者中明显低于对照组 (比值比 (OR)=0.78,95%置信区间 (CI): 0.62-0.98,p=0.034;OR=0.58,95%CI: 0.42-0.80,p=0.001;OR=0.77,95%CI: 0.66-0.90,p=0.001)。rs641101 多态性与 CAD 无相关性。单体型分析显示,rs351855 和 rs641101 AG 单体型在 CAD 患者中的频率也较低 (OR=0.79,95%CI: 0.67-0.92,p=0.002)。我们的数据表明,FGFR4 rs351855 (Gly388Arg) 多态性和 AG 单体型 (rs351855 和 rs641101) 可能是中国人群 CAD 的保护因素,并表明单个基因多态性在不同疾病中可能具有不同的功能。

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