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血管紧张素转换酶基因 2350 G/A 多态性与汉族原发性高血压患者心房颤动易感性的关系。

Angiotensin-converting enzyme gene 2350 G/A polymorphism and susceptibility to atrial fibrillation in Han Chinese patients with essential hypertension.

机构信息

Department of Cardiology, Hospital of Nantong University, Nantong, China.

出版信息

Clinics (Sao Paulo). 2013 Nov;68(11):1428-32. doi: 10.6061/clinics/2013(11)08.

Abstract

OBJECTIVE

The angiotensin-converting enzyme gene is one of the most studied candidate genes related to atrial fibrillation. Among the polymorphisms of the angiotensin-converting enzyme gene, the 2350 G/A polymorphism (rs4343) is known to have the most significant effects on the plasma angiotensin-converting enzyme concentration. The aim of the present study was to investigate the association of the angiotensin-converting enzyme 2350 G/A polymorphism with atrial fibrillation in Han Chinese patients with essential hypertension.

METHODS

A total of 169 hypertensive patients were eligible for this study. Patients with atrial fibrillation (n = 75) were allocated to the atrial fibrillation group, and 94 subjects without atrial fibrillation were allocated to the control group. The PCR-based restriction fragment length polymorphism technique was used to assess the genotype frequencies.

RESULTS

The distributions of the angiotensin-converting enzyme 2350 G/A genotypes (GG, GA, and AA, respectively) were 40.43%, 41.49%, and 18.08% in the controls and 18.67%, 46.67%, and 34.66% in the atrial fibrillation subjects (p = 0.037). The frequency of the A allele in the atrial fibrillation group was significantly greater than in the control group (58.00% vs. 38.83%, p = 0.0007). Compared with the wild-type GG genotype, the GA and AA genotypes had an increased risk for atrial fibrillation. Additionally, atrial fibrillation patients with the AA genotype had greater left atrial dimensions than the patients with the GG or GA genotypes (p<0.01 and p<0.05, respectively).

CONCLUSIONS

The results obtained in this study indicate that the angiotensin-converting enzyme 2350 G/A polymorphism is associated with atrial fibrillation and that the A allele shows an increased risk for atrial fibrillation in Han Chinese patients with essential hypertension.

摘要

目的

血管紧张素转换酶基因是与心房颤动相关的最受研究的候选基因之一。在血管紧张素转换酶基因的多态性中,2350 G/A 多态性(rs4343)已知对血浆血管紧张素转换酶浓度有最显著的影响。本研究旨在探讨汉族原发性高血压患者血管紧张素转换酶 2350 G/A 多态性与心房颤动的关系。

方法

共有 169 名高血压患者符合本研究条件。心房颤动患者(n=75)被分配到心房颤动组,94 名无心房颤动的患者被分配到对照组。采用基于 PCR 的限制性片段长度多态性技术评估基因型频率。

结果

对照组的血管紧张素转换酶 2350 G/A 基因型(分别为 GG、GA 和 AA)分布为 40.43%、41.49%和 18.08%,而心房颤动组分别为 18.67%、46.67%和 34.66%(p=0.037)。心房颤动组 A 等位基因的频率明显高于对照组(58.00%比 38.83%,p=0.0007)。与野生型 GG 基因型相比,GA 和 AA 基因型增加了心房颤动的风险。此外,AA 基因型的心房颤动患者的左心房内径大于 GG 或 GA 基因型的患者(p<0.01 和 p<0.05,分别)。

结论

本研究结果表明,血管紧张素转换酶 2350 G/A 多态性与心房颤动有关,A 等位基因增加了汉族原发性高血压患者发生心房颤动的风险。

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本文引用的文献

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Novel GATA5 loss-of-function mutations underlie familial atrial fibrillation.
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