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血管紧张素转换酶基因和血管紧张素原基因位点的变异与血压的关系。

Variation at the angiotensin-converting enzyme gene and angiotensinogen gene loci in relation to blood pressure.

作者信息

Kiema T R, Kauma H, Rantala A O, Lilja M, Reunanen A, Kesäniemi Y A, Savolainen M J

机构信息

Biocenter Oulu, Finland.

出版信息

Hypertension. 1996 Dec;28(6):1070-5. doi: 10.1161/01.hyp.28.6.1070.

Abstract

To investigate whether the polymorphisms in the angiotensin-converting enzyme and angiotensinogen genes are associated with hypertension, we carried out a case-control study of 508 hypertensive and 523 control subjects randomly selected from the Social Insurance Institution register. The cohorts were well characterized and matched for age and sex. The insertion/ deletion polymorphism of the angiotensin-converting enzyme gene and the methionine-->threonine variant at position 235 of the angiotensinogen gene were determined by the polymerase chain reaction technique. The allele frequencies and genotype distributions of both polymorphisms were similar in hypertensive and control subjects. Systolic and diastolic pressures adjusted for age, body mass index, and alcohol consumption did not differ significantly between the different genotypes of the angiotensin-converting enzyme and angiotensinogen genes. The variation at the angiotensinogen and angiotensin-converting enzyme genes did not have any statistically significant synergistic effect on blood pressure levels. In conclusion, the polymorphisms in the reninangiotensin cascade genes do not confer a significantly increased risk for the development of hypertension in this middle-aged, population-based cohort.

摘要

为研究血管紧张素转换酶基因和血管紧张素原基因的多态性是否与高血压相关,我们对从社会保险机构登记册中随机选取的508名高血压患者和523名对照者进行了一项病例对照研究。这些队列在年龄和性别方面特征明确且相互匹配。采用聚合酶链反应技术测定血管紧张素转换酶基因的插入/缺失多态性以及血管紧张素原基因第235位的甲硫氨酸→苏氨酸变异。高血压患者和对照者中这两种多态性的等位基因频率和基因型分布相似。校正年龄、体重指数和饮酒量后的收缩压和舒张压在血管紧张素转换酶基因和血管紧张素原基因的不同基因型之间无显著差异。血管紧张素原基因和血管紧张素转换酶基因的变异对血压水平没有任何统计学上的显著协同作用。总之,在这个基于人群的中年队列中,肾素-血管紧张素级联基因的多态性不会显著增加患高血压的风险。

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