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伊朗人群中血管紧张素转换酶基因变异与冠状动脉疾病的关联。

Association of angiotensin-converting enzyme gene variations with coronary artery disease in the Iranian population.

作者信息

Ghaffarzadeh Ayda, Nemati Mohadeseh, Hassan-Nejhad Mahsa, Khadem-Vatani Kamal, Baghal-Sadriforoush Sahar, Bagheri Morteza

机构信息

Cellular and Molecular Research Center, Cellular and Molecular Medicine Research Institute, Urmia University of Medical Sciences, Urmia, Iran.

Department of Clinical Biochemistry, Faculty of Medicine, Urmia University of Medical Sciences, Urmia, Iran.

出版信息

ARYA Atheroscler. 2023 Jan;19(1):12-16. doi: 10.48305/arya.2022.11869.2692.

Abstract

BACKGROUND

The purpose of this study was to identify the angiotensin-converting enzyme (ACE) gene (I/D) variations in CAD patients and healthy controls in an Iranian population (West Azerbaijan province of Iran).

METHOD

This cross-sectional study included 95 CAD patients and 203 healthy controls. ACE I/D polymorphisms were assessed using PCR, and their frequency was determined.

RESULTS

There were 298 people, 95 CAD patients, and 203 controls, with an average age of 50.96±3.45 and 51.14±10.20. We discovered that the frequency of the D allele was significantly higher in CAD patients than in controls (P = 0.0009). In contrast, the frequency of the I allele was significantly higher in controls than in CAD patients (P = 0.0009). The D allele carriers genotypes (DD + ID) were more frequent in the CAD patients than in the control group (P = 0.008). The ACE II genotype-state carriers were more common in the control group than in CAD patients (P = 0.008). However, in the case of the ACE ID genotype, no significant differences were not found in the tested groups (P = 0.47).

CONCLUSIONS

These findings suggest that individuals with the ACE DD genotype are predisposed to CAD, whereas individuals with the ACE II genotype state are protected.

摘要

背景

本研究旨在确定伊朗人群(伊朗西阿塞拜疆省)中冠心病(CAD)患者和健康对照者的血管紧张素转换酶(ACE)基因(I/D)变异情况。

方法

这项横断面研究纳入了95例CAD患者和203名健康对照者。采用聚合酶链反应(PCR)评估ACE I/D多态性,并确定其频率。

结果

共有298人,其中95例CAD患者和203名对照者,平均年龄分别为50.96±3.45岁和51.14±10.20岁。我们发现,CAD患者中D等位基因的频率显著高于对照组(P = 0.0009)。相反,对照组中I等位基因的频率显著高于CAD患者(P = 0.0009)。CAD患者中D等位基因携带者基因型(DD + ID)比对照组更常见(P = 0.008)。ACE II基因型状态携带者在对照组中比CAD患者更常见(P = 0.008)。然而,在ACE ID基因型方面,测试组之间未发现显著差异(P = 0.47)。

结论

这些发现表明,ACE DD基因型个体易患CAD,而ACE II基因型状态个体受到保护。

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