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Insertion/deletion polymorphism in the angiotensin-converting enzyme gene inmyocardial infarction survivors.

机译:心肌梗死幸存者血管紧张素转换酶基因的插入/缺失多态性。

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INTRODUCTION: Insertion/deletion (I/D) polymorphism of the angiotensin-convertingenzyme (ACE) gene influenced the plasma concentration of the ACE, and is D allele have been repetitivelysuggested as a risk factor for myocardial infarction (MI). MATERIAL AND METHODS: Two hundert thirty sixmale myocardial infarction survivors under 65 years and with body mass index and total plasma cholesterollevels under 95% of the Czech population were included in the study. As control group, 302 male controls(1% randomly selected group from the Czech population) were genotyped. I/D polymorphism in the ACE genewas determined using polymerase chain reaction. RESULTS: The prevalence of the I/I, I/D and D/D genotypeswas 0.218, 0.494 and 0.288, in the control group, and 0.178, 0.538 and 0.284, in the myocardial survivors,respectively. The male Czech population has the similar frequency of insertion and deletion alleles comparedto other Caucasian populations. The frequencies of the alleles and genotypes of the ACE gene did notdiffer significantly between MI survivors and a control sample of the Czech population. CONCLUSION: Itwas shown that the I/D polymorphism in the gene for ACE is not a genetic risk factor for myocardial infarctionin the Czech population.
机译:简介:血管紧张素转换酶(ACE)基因的插入/缺失(I / D)多态性影响ACE的血浆浓度,D等位基因已被重复认为是心肌梗塞(MI)的危险因素。材料与方法:本研究纳入了2名65岁以下,体重指数和总血浆胆固醇水平低于95%的捷克人群的36名男性心肌梗死幸存者。作为对照组,对302名男性对照组(从捷克人群中随机选择的1%)进行基因分型。 ACE基因中的I / D多态性通过聚合酶链反应确定。结果:对照组中I / I,I / D和D / D基因型的患病率分别为0.218、0.494和0.288,心肌存活者的I / I,I / D和D / D基因型的患病率分别为0.178、0.538和0.284。与其他白种人人口相比,捷克男性人口具有相似的插入和缺失等位基因频率。心肌梗死幸存者与捷克人群的对照样本之间,ACE基因的等位基因频率和基因型没有明显差异。结论:研究表明,ACE基因的I / D多态性不是捷克人群心肌梗死的遗传危险因素。

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