冠状动脉搭桥术后静脉桥狭窄和新生易损斑块形成机制的研究进展
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(1.大连医科大学附属第一医院心内科,辽宁省大连市 116011;2.烟台市莱阳中心医院心内科,山东省莱阳市 265200)

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朱亚男,硕士,住院医师,研究方向为冠心病防治的流行病学及生理学研究,E-mail为dalianzyn@163.com。通信作者张波,博士,主任医师,硕士研究生导师,研究方向为冠心病的介入诊断与治疗、冠心病和心力衰竭的临床和基础,E-mail为zhangbo2674@163.com。

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基金项目:

辽宁省省直医院改革重点临床科室诊疗能力建设项目(LNCCC-D18-2015);大连市科技计划项目(2015E12SF168)


Research progress on pathogenesis of vein bypass graft stenosis and new vulnerable plaque lesion after coronary artery bypass graft
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1.Department of Cardiology, First Affiliated Hospital of Dalian Medical University, Dalian, Liaoning 116011, China;2.Department of Cardiology, Laiyang Central Hospital, Laiyang, Shandong 265200, China)

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    摘要:

    冠状动脉搭桥术术后发生桥血管病变是一种常见的现象,血栓形成、内皮功能障碍、血管痉挛和氧化应激是导致病变的重要机制。相比于动脉桥,静脉桥更易于发生病变,这与静脉本身的解剖形态和功能特征有着很大的关系。急性血栓形成、血管内膜增生和易损斑块形成是静脉桥不同时期发生病变的重要机制。使用抗血小板和调脂药物等冠心病二级预防药物有助于提高桥血管的开通率。寻找桥血管病变的预测因子及相关基因通路有望从细胞及分子学水平为静脉桥疾病提供新的研究方向。本文拟对冠状动脉搭桥术后发生静脉桥狭窄和新生易损斑块病变形成机制的研究进展作一综述。

    Abstract:

    Graft lesions after coronary artery bypass graft are the common phenomenon. Thrombosis, endothelial dysfunction, vasospasm, and oxidative stress are important mechanisms leading to the lesions. Compared with arterial bypass graft, venous bypass graft is more susceptible to lesions, which is closely related to the anatomical morphology and functional characteristics of veins themselves. Acute thrombosis, intimal hyperplasia and vulnerable plaque formation are important mechanisms of vein graft lesions during different stages. Secondary prevention drugs such as antiplatelet and lipid-lowering drugs can improve the patency rate of bypass grafts. The search for predictors and related gene pathways of vein graft disease is expected to provide new research directions for vein graft disease at cellular and molecular levels. The review summarizes the research progress on pathogenesis of vein bypass graft stenosis and new vulnerable plaque lesions after coronary artery bypass graft.

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朱亚男,张波.冠状动脉搭桥术后静脉桥狭窄和新生易损斑块形成机制的研究进展[J].中国动脉硬化杂志,2019,27(4):310~314.

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  • 收稿日期:2018-08-27
  • 最后修改日期:2018-11-13
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  • 在线发布日期: 2019-04-08