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PCSK9——高胆固醇血症的新靶点

PCSK9——New Target of Hypercholesterolemia

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【作者】 宋三兵董旭南

【Author】 SONG San-bing;DONG Xu-nan;Department of Emergency Intensive Care Unit,the First Affliated Hospital of Xinjiang Medical University;

【机构】 新疆医科大学第一附属医院急救中心重症监护室

【摘要】 前蛋白转化酶枯草溶菌素9基因(PCSK9)是近十年来发现的一种新的致病基因,基因突变主要有功能获得型、功能缺失型,前者通过介导肝脏低密度脂蛋白受体(LDLR)的降解、减少LDLR的数量、降低肝脏对LDLR的清除,引起高胆固醇血症,在脂质代谢中发挥着重要作用。血清中低密度脂蛋白胆固醇(LDL-C)水平与冠心病的发生风险呈正相关,使用他汀类等降脂药物后,大大降低了高胆固醇血症患者的LDL-C及冠心病的发病风险,但仍有大部分患者LDL-C未达到理想目标。动物实验及临床试验显示,PCSK9抑制剂可大幅度降低各种高胆固醇患者的LDL-C水平,给高胆固醇血症患者带来了福音;但其发挥作用的确切机制需进一步研究。

【Abstract】 Proprotein convertase subtilisin / kexin 9 gene( PCSK9) is a new pathogenic gene discovered over the past decade,and there are mainly two gene mutations: gaining function,losing function,the former regulates liver low-density lipoprotein receptor( LDLR) degradation,to reduce the level of LDLR,and the reduced hepatic clearance of LDLR,causes hypercholesterolemia,which plays an important role in lipid metabolism. Serum low-density lipoprotein cholesterol( LDL-C) concentration and the risk of coronary heart disease are positively correlated,and the use of statins and other lipid-lowering drugs,greatly reduce the level of LDL-C and the risk of coronary heart disease in hypercholesterolemia,though the majority of patients do not achieve the desired LDL-C goal. Animal experiments and clinical trials show that PCSK9 inhibitors can significantly reduce LDL-C concentrations in patients with hypercholesterolemia,benefitting the patients,though the exact mechanism needs further studies.

  • 【文献出处】 医学综述 ,Medical Recapitulate , 编辑部邮箱 ,2016年06期
  • 【分类号】R589.2
  • 【被引频次】8
  • 【下载频次】618
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