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血管紧张素转换酶基因插入/缺失多态性与代谢综合征患者勃起功能障碍之间的关联。

Association between the insertion/deletion polymorphism of the angiotensin-converting enzyme gene and erectile dysfunction in patients with metabolic syndrome.

作者信息

Mazo E B, Gamidov S I, Mamedov M N, Iremashvili V V

机构信息

Department of Urology, Russian State Medical University, Moscow, Russia.

出版信息

Int J Impot Res. 2008 Jan-Feb;20(1):68-72. doi: 10.1038/sj.ijir.3901598. Epub 2007 Aug 2.

Abstract

This study was designed to investigate whether angiotensin-converting enzyme (ACE) insertion/deletion (I/D) polymorphism is associated with erectile dysfunction (ED) in Russian men with metabolic syndrome (MS). A total of 331 men with MS were studied. All patients underwent complex evaluation including the International Index of Erectile Function (IIEF) questionnaire. The ACE I/D polymorphism was determined by polymerase chain reaction. Overall, 182 men (55.0%) had ED according to the IIEF erectile function domain score. In the ED group, the prevalence of DD genotype was found to be significantly higher compared to the non-ED group (P<0.001). In both groups, patients with DD genotype were significantly younger than patients with other genotypes (P<0.001). In addition, in the ED group, the disease affected patients with DD genotype at a significantly younger age (P<0.001). Obtained results give evidence to support the finding that the D allele is a risk factor for the micro- and macrovascular diseases.

摘要

本研究旨在调查血管紧张素转换酶(ACE)插入/缺失(I/D)多态性是否与患有代谢综合征(MS)的俄罗斯男性勃起功能障碍(ED)相关。共研究了331名患有MS的男性。所有患者均接受了包括国际勃起功能指数(IIEF)问卷在内的综合评估。通过聚合酶链反应确定ACE I/D多态性。总体而言,根据IIEF勃起功能领域评分,182名男性(55.0%)患有ED。在ED组中,发现DD基因型的患病率显著高于非ED组(P<0.001)。在两组中,DD基因型的患者明显比其他基因型的患者年轻(P<0.001)。此外,在ED组中,该疾病在DD基因型的患者中发病年龄明显更小(P<0.001)。获得的结果为支持D等位基因是微血管和大血管疾病的危险因素这一发现提供了证据。

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