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动脉僵硬度的遗传学与病理生理学

Genetics and pathophysiology of arterial stiffness.

作者信息

Lacolley Patrick, Challande Pascal, Osborne-Pellegrin Mary, Regnault Veronique

机构信息

INSERM, U961, Faculté de Médecine, 9 avenue de la forêt de Haye, B.P. 184, 54500 Vandoeuvre-les-Nancy cedex, France.

出版信息

Cardiovasc Res. 2009 Mar 1;81(4):637-48. doi: 10.1093/cvr/cvn353. Epub 2008 Dec 20.

Abstract

Arterial stiffness is a cardiovascular risk factor that is independent of arterial pressure. Clinically, carotid-femoral pulse wave velocity (PWV) is the gold-standard parameter of arterial stiffness. Recent genetic studies have revealed specific genes that contribute to arterial stiffening. Here we review the recent findings on genome-wide linkage analyses and candidate gene polymorphism association studies. We also focus on the latest advances in the identification of gene variants affecting PWV using high density array single nucleotide polymorphism technology in a recent genome-wide association (GWA) study. Linkage and polymorphism studies revealed a first group of genes affecting the renin-angiotensin-aldosterone system, elastic fibre structural components, metalloproteinases, and the NO pathway. A second group of genes, identified by polymorphism association studies and possibly involved in the pathophysiology of arterial stiffness, includes beta-adrenergic receptors, endothelin receptors, and inflammatory molecules. The last group of genes, identified by GWA studies and unrelated to currently suspected mechanisms of arterial stiffness, may target transcriptional pathways controlling gene expression, differentiation of vascular smooth muscle cells, apoptosis of endothelial cells, or the immune response within the vascular wall.

摘要

动脉僵硬度是一种独立于动脉压的心血管危险因素。临床上,颈股脉搏波速度(PWV)是动脉僵硬度的金标准参数。最近的基因研究已经揭示了导致动脉僵硬化的特定基因。在此,我们综述了全基因组连锁分析和候选基因多态性关联研究的最新发现。我们还重点关注了在最近一项全基因组关联(GWA)研究中,使用高密度阵列单核苷酸多态性技术鉴定影响PWV的基因变异方面的最新进展。连锁和多态性研究揭示了第一组影响肾素-血管紧张素-醛固酮系统、弹性纤维结构成分、金属蛋白酶和NO途径的基因。通过多态性关联研究鉴定出的、可能参与动脉僵硬度病理生理学的第二组基因包括β-肾上腺素能受体、内皮素受体和炎症分子。通过GWA研究鉴定出的、与目前怀疑的动脉僵硬度机制无关的最后一组基因,可能靶向控制基因表达、血管平滑肌细胞分化、内皮细胞凋亡或血管壁内免疫反应的转录途径。

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