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首页> 外文期刊>Journal of hypertension >Association between angiotensin converting enzyme gene polymorphism and carotid atherosclerosis.
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Association between angiotensin converting enzyme gene polymorphism and carotid atherosclerosis.

机译:血管紧张素转换酶基因多态性与颈动脉粥样硬化之间的关联。

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摘要

OBJECTIVE: Variations in the angiotensin converting enzyme (ACE) gene have been implicated in cardiovascular pathology. Therefore, the association between the intima-media thickness (IMT) of the carotid artery and the insertion/ deletion (I/D) polymorphism of the ACE gene was investigated. SUBJECTS: Three hundred men and 300 women were selected randomly from the middle-aged population living in the town Oulu, Finland, of whom 515 subjects (85.8%) participated. METHODS: The IMT of the carotid arteries was determined by bilateral B-mode ultrasonography. IMT values were adjusted for gender, age, height, plasma low-density lipoprotein cholesterol level, smoking and systolic blood pressure. The I/D polymorphism of the ACE gene was determined by polymerase chain reaction. RESULTS: Among non-smokers, the subjects with the DD genotype had significantly higher carotid IMT than did those with II or ID. The association was found also in combined IMT plaque values. In the total population the association was weaker and it was absent in current smokers. Genotype could explain 1.3-2.7% of the variance of carotid IMT in non-smokers. No association between the amount or size of carotid plaques and genotype was observed. CONCLUSIONS: Variations at the ACE gene locus contribute to the degree of the early changes in carotid atherosclerosis in the population. The gene effect is, however, masked by stronger effects of environmental factors such as smoking. The lack of association between atherosclerotic plaques and genotypes may reflect different mechanisms being involved in plaque development and early arterial wall thickening.
机译:目的:血管紧张素转化酶(ACE)基因的变异与心血管病理有关。因此,研究了颈动脉内膜中层厚度(IMT)与ACE基因的插入/缺失(I / D)多态性之间的关联。受试者:从居住在芬兰奥卢镇的中年人中随机选择了300名男性和300名女性,其中515名受试者(85.8%)参加了试验。方法:通过双侧B超检查确定颈动脉的IMT。根据性别,年龄,身高,血浆低密度脂蛋白胆固醇水平,吸烟和收缩压调整IMT值。 ACE基因的I / D多态性通过聚合酶链反应确定。结果:在非吸烟者中,DD基因型受试者的颈动脉IMT明显高于II或ID受试者。在组合的IMT斑块值中也发现了这种关联。在总人口中,该关联性较弱,在当前吸烟者中不存在。基因型可以解释非吸烟者颈动脉IMT变异的1.3-2.7%。颈动脉斑块的数量或大小与基因型之间没有关联。结论:ACE基因位点的变异有助于人群颈动脉粥样硬化的早期改变。但是,基因效应被诸如吸烟等环境因素的较强效应所掩盖。动脉粥样硬化斑块和基因型之间缺乏关联可能反映了参与斑块形成和早期动脉壁增厚的不同机制。

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