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血管紧张素转换酶基因的缺失/插入多态性作为斯洛文尼亚冠心病患者的一个危险因素。

Deletion/insertion polymorphism in the angiotension-converting enzyme gene as a risk factor in the Slovenian patients with coronary heart disease.

作者信息

Peterlin B, Petrovic D, Zorc M, Keber I

机构信息

Department of Obstetrics and Gynecology, UMC Ljubljana, Slovenia.

出版信息

Pflugers Arch. 2000;439(3 Suppl):R40-1.

Abstract

The angiotensin-converting enzyme (ACE) plays by degradation of angiotensin I and bradykinin, an important role in modulations of smooth muscle proliferation and vascular tone. Typical plasma levels of ACE accompany the I/D polymorphism; however, a controversy exists as to whether the DD genotype of the ACE polymorphism affects the risk for the development of coronary heart disease (CHD). We compared the I/D polymorphism in 171 Slovenian CHD patients that were younger than 55 years with 134 healthy control individuals. The DD genotype is associated with a 2.3-fold increase in the risk for CHD.

摘要

血管紧张素转换酶(ACE)通过降解血管紧张素I和缓激肽,在调节平滑肌增殖和血管张力方面发挥重要作用。ACE的典型血浆水平与I/D多态性相关;然而,关于ACE多态性的DD基因型是否会影响冠心病(CHD)的发病风险存在争议。我们比较了171名年龄小于55岁的斯洛文尼亚冠心病患者与134名健康对照者的I/D多态性。DD基因型与冠心病风险增加2.3倍相关。

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