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精氨酸酶1基因多态性与心肌梗死风险及颈总动脉内膜中层厚度的关联

Association of arginase 1 gene polymorphisms with the risk of myocardial infarction and common carotid intima media thickness.

作者信息

Dumont Julie, Zureik Mahmoud, Cottel Dominique, Montaye Michèle, Ducimetière Pierre, Amouyel Philippe, Brousseau Thierry

出版信息

J Med Genet. 2007 Aug;44(8):526-31. doi: 10.1136/jmg.2006.047449. Epub 2007 Mar 16.

Abstract

BACKGROUND

Recently, it was suggested that arginase (ARG)1 plays an important role in atherogenesis. However, because of its complex functions depending on vascular cell type, its impact on atherogenesis remains unclear.

OBJECTIVE

To evaluate the association between ARG1 polymorphisms and phenotypes related to atherosclerosis.

METHODS

Among 10 ARG1 polymorphisms selected from databases, 4 single-nucleotide polymorphisms (rs2781666; rs2781667; rs2781668; rs17599586) were tested for association with myocardial infarction (MI) in a case-control study (350 cases vs 581 controls), and with common carotid artery (CCA) intima-media thickness (CCA-IMT) in an independent sample of 963 subjects (Etude du Vieillissement Artériel (EVA) study).

RESULTS

The genotype distribution of the rs2781666 G/T polymorphism differed significantly between MI cases and controls (p = 0.005), and the risk of MI was consistently increased for both GT heterozygotes (OR (95% CI) 1.5 (1.1 to 2.0)) and TT homozygotes (OR (95% CI) 2.2 (1.1 to 4.4)). In the EVA study, the rs2781666 polymorphism was also associated with an increase in CCA-IMT (p = 0.010), a surrogate marker of MI.

CONCLUSIONS

The ARG1 rs2781666 polymorphism was consistently associated with MI and an increased CCA-IMT. These findings reinforce the hypothesis of a significant role of ARG1 in vascular pathophysiology.

摘要

背景

最近,有人提出精氨酸酶(ARG)1在动脉粥样硬化形成中起重要作用。然而,由于其功能因血管细胞类型而异,其对动脉粥样硬化形成的影响仍不清楚。

目的

评估ARG1基因多态性与动脉粥样硬化相关表型之间的关联。

方法

在从数据库中选择的10个ARG1基因多态性中,对4个单核苷酸多态性(rs2781666;rs2781667;rs2781668;rs17599586)进行病例对照研究(350例病例对581例对照),以检测其与心肌梗死(MI)的关联,并在963名受试者的独立样本(动脉老化研究(EVA))中检测其与颈总动脉(CCA)内膜中层厚度(CCA-IMT)的关联。

结果

rs2781666 G/T基因多态性的基因型分布在MI病例和对照之间有显著差异(p = 0.005),GT杂合子(OR(95%CI)1.5(1.1至2.0))和TT纯合子(OR(95%CI)2.2(1.1至4.4))发生MI的风险均持续增加。在EVA研究中,rs2781666基因多态性也与CCA-IMT增加相关(p = 0.010),CCA-IMT是MI的替代标志物。

结论

ARG1 rs2781666基因多态性与MI及CCA-IMT增加持续相关。这些发现强化了ARG1在血管病理生理学中起重要作用的假说。

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