ACE gene polymorphism and coronary restenosis.

C Bauters, P Amouyel, M E Bertrand
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引用次数: 8

Abstract

In humans, circulating levels of angiotensin-converting enzyme (ACE) are linked with an insertion (I)/deletion (D) polymorphism in the ACE gene: DD genotype bearers have higher levels of ACE than either ID or II genotype bearers. Recent studies have suggested that the ACE DD genotype might be associated with a higher risk of coronary artery disease. The aim of this paper is to review studies on the influence of the I/D polymorphism on coronary restenosis. The renin-angiotensin system has been implicated in the pathogenesis of neointimal hyperplasia in experimental models. In humans, the I/D polymorphism is not associated with restenosis after balloon angioplasty, but is strongly associated with restenosis after coronary stent implantation. This may be explained by the fact that the contribution of neointimal hyperplasia to restenosis is much more important after coronary stent implantation than after balloon angioplasty.

ACE基因多态性与冠状动脉再狭窄。
在人类中,血管紧张素转换酶(ACE)的循环水平与ACE基因的插入(I)/缺失(D)多态性有关:DD基因型携带者的ACE水平高于ID或II基因型携带者。最近的研究表明,ACE DD基因型可能与冠状动脉疾病的高风险相关。本文就I/D多态性对冠状动脉再狭窄影响的研究进展进行综述。肾素-血管紧张素系统在实验模型中涉及到新内膜增生的发病机制。在人类中,I/D多态性与球囊血管成形术后再狭窄无关,但与冠状动脉支架植入术后再狭窄密切相关。这可能是由于冠状动脉支架植入术后新生内膜增生对再狭窄的贡献比球囊血管成形术更重要。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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