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男性早发性冠心病与血管紧张素原基因启动子区域-217G/A和-152G/A多态
引用本文:刘艳,沈卫峰,金玮,盛海辉,金璘,沈亚云,黄薇,于金德.男性早发性冠心病与血管紧张素原基因启动子区域-217G/A和-152G/A多态[J].内科理论与实践,2007,2(3):168-171.
作者姓名:刘艳  沈卫峰  金玮  盛海辉  金璘  沈亚云  黄薇  于金德
作者单位:上海交通大学医学院附属瑞金医院心内科上海交通大学心血管病研究所,上海交通大学医学院附属瑞金医院心内科上海交通大学心血管病研究所,上海交通大学医学院附属瑞金医院心内科上海交通大学心血管病研究所,国家人类基因组南方研究中心,国家人类基因组南方研究中心,国家人类基因组南方研究中心,国家人类基因组南方研究中心,上海交通大学医学院附属瑞金医院心内科上海交通大学心血管病研究所 上海200025,上海200025,上海200025,上海201203,上海201203,上海201203,上海201203,上海200025
基金项目:国家自然科学基金 , 上海市科委资助项目 , 上海市青年科技启明星计划
摘    要:目的:研究血管紧张素原(angiotensinogen,AGT)基因启动子区域的-217G/A和-152G/A多态与上海地区汉族男性早发性冠心病(CAD)的相关性。方法:采用多重SNaPshot反应,在100例男性早发性CAD患者和100名健康男性对照者中,对AGT基因启动子区域的-217G/A和-152G/A多态进行基因分型。结果:-217G/A多态AA、AG和GG基因型在CAD组中的分布与对照组相比有显著性差异(P=0.039),CAD组的A等位基因频率较对照组亦显著增加(P=0.012),A等位基因携带者早发性CAD的发病危险是非携带者的1.913倍(95%CI1.151~3.182)。-152G/A多态的基因型分布在2组间的差异无统计学意义(P=0.154),其A、G等位基因频率2组相比有差异(P=0.044)。在多支病变组中,-217G/A多态的基因型分布及其等位基因频率2组相比均有显著性差异(分别为P=0.010和P=0.005),且A等位基因携带者发生多支病变的危险是非携带者的2.307倍(95%CI1.274~4.179)。结论:在上海地区的汉族男性人群中,AGT基因-217G/A和-152G/A多态可能是其早发性CAD的遗传性危险因素,且-217G/A多态可能还与冠状动脉粥样硬化的病变程度相关。

关 键 词:血管紧张素原  基因  多态性  早发性冠心病  
文章编号:1673-6087(2007)03-0168-04
修稿时间:2006-02-12

-217G/A and -152G/A polymorphisms in angiotensinogen gene promoter and their relationship with male early onset coronary artery disease
LIU Yan,SHEN Wei-feng,JIN Wei,SHENG Hai-hui,JIN Lin,SHEN Ya-yun,HUANG Wei,YU Jin-de.-217G/A and -152G/A polymorphisms in angiotensinogen gene promoter and their relationship with male early onset coronary artery disease[J].Joournal of Internal Medicine Concepts& Practice,2007,2(3):168-171.
Authors:LIU Yan  SHEN Wei-feng  JIN Wei  SHENG Hai-hui  JIN Lin  SHEN Ya-yun  HUANG Wei  YU Jin-de
Institution:1. Department of Cardiology, Ruijin Hospital, Institute of Cardiology, Shanghai Jiaotong University School of Medicine, Shanghai 200025, China; 2.Chinese National Human Genome Center at Shanghai, Shanghai 201203, China
Abstract:Objective To determine the -217G/A and -152G/A polymorphisms in the promoter region of angiotensinogen(AGT) gene, and their relationship with Han male early on,set coronary artery disease(CAD) in Shanghai region. Methods The genotypes of -217G/A and -152G/A polymorphisms in 100 male early on,set CAD patients and 100 healthy male as control group were analysed by SNaPshot Multiplex Kit. Results The genotype distribution of -217G/A polymorphism was obviously different between the CAD group (AA=7,AG=35,GG=58) and the control group (AA=4,AG=21, GG=75,P=0.039). CAD patients demonstrated a significantly increased A allele frequency than healthy controls (24.50% vs 14.50%, P=0.012), the relative risk of early on,set CAD in population with A allele was 1.913 (95%CI 1.151-3.182). Yet, no significant difference in the genotype distribution of -152G/A polymorphism was observed between these two groups (P=0.154). Frequencies of A and G alleles were different between CAD and control populations (5.00% vs 3.00%; 95.00% vs 97.00%, P=0.044). Similarly, the genotype distribution and alleles frequency of -217G/A polymorphism were obviously different between group of double,vessel disease (DVD), triple,vessel disease (TVD) and control group (P=0.010, P=0.005). The relative risk of multi,vessel CAD in men with A allele was 2.307 (95%CI 1.274-4.179). Conclusions -217G/A and -152G/A polymorphisms of AGT gene might be served as genetic risk factors for early on,set CAD in Han male population in Shanghai region. Furthermore, -217G/A polymorphism is closely related with the extent of coronary atherosclerosis.
Keywords:Angiotensinogen  Gene  Polymorphism  Early on-set  Coronary artery disease
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