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作 者:陈德[1,2] 范维琥[1,2] 张眉 施海明[1,2] 李勇[1,2] 顾学范 戴瑞鸿[1,2]
机构地区:[1]上海医科大学华山医院心内科 [2]上海第二医科大学上海市儿科医学研究所
出 处:《上海医科大学学报》1998年第2期83-86,共4页Journal of Fudan University(Medical Science)
摘 要:目的研究血管紧张素原(AGT)基因M235T分子变异与中国人冠心病(CHD)发生的关系。方法采用多聚酶链反应(PCR)、限制性片段长度多态性分析,对76例CHD患者和76例无CHD证据的对照组进行AGT基因M235T等位基因检测。结果CHD患者AGT基因235TT型(0.70)和T235等位基因(0.82)的频率显著高于对照组(分别为0.42和0.63,P=0.002和P<0.01)。经校正CHD的主要危险因素后,AGT基因235TT型仍可显著增加CHD发生的危险性(比数比为3.56,P=0.012)。结论中国人AGT基因M235T分子变异与CHD显著相关,AGT基因235TT型可能是CHD的重要危险因素之一。URPOSE To study whether a molecular variant of the angiotensinogen (AGT) gene with threonine instead of methionine at position 235 (i.e., with M235T polymorphism) was related with coronary heart disease (CHD) in a Chinese population.METHODS M235T polymorphism in exon 2 of AGT gene was determined by polymerase chain reaction and restriction fragment length polymorphism (PCR-RFLP) in 76 patients with CHD (75% of MI) and 76 non-CHD subjects as control.RESULTS The frequencies of T235 allele (0.82) and 235TT genotype (0.70) were higher in the CHD group than that of the control group (0.63 and 0.42 P=0.002 and P<0.01 respectively). AGT gene 235TT genotype was shown to significantly increase. The risk of CHD (odds ratio 3.56, P=0.012) in analysis adjusted for several main CHD risk factor.CONCLUSIONS There is a significant relationship between AGT gene 235TT genotype and CHD. This genotype might be an independent risk factor for CHD in Chinese population.
分 类 号:R541.402[医药卫生—心血管疾病]
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