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[高密度脂蛋白:心血管疾病的阴阳两面]

[HDL: the yin-yang of cardiovascular disease].

作者信息

Leança Camila Canteiro, Passarelli Marisa, Nakandakare Edna R, Quintão Eder C R

机构信息

Laboratório de Lípides, Disciplina de Endocrinologia e Metabologia, Hospital das Clínicas, Faculdade de Medicina, Universidade de São Paulo, SP, Brasil.

出版信息

Arq Bras Endocrinol Metabol. 2010 Dec;54(9):777-84. doi: 10.1590/s0004-27302010000900002.

DOI:10.1590/s0004-27302010000900002
PMID:21340169
Abstract

Epidemiological studies demonstrate an inverse correlation between plasma HDL-cholesterol (HDL-C) concentration and incidence of cardiovascular disease (CVD). The antiatherogenic role of HDL has been attributed to its anti-inflammatory, antithrombotic and antioxidant properties, besides its participation in the reverse cholesterol transport (RCT), whereby cholesterol from peripheral tissues (including macrophages of the arterial intima) is delivered to the liver for excretion in bile. Due to these actions, HDL-C has evolved as an attractive target for prevention of CVD. However, the failure of torcetrapib, drug that substantially increases HDL-C levels, in preventing CVD and data from studies with animal models and with carriers of monogenic disorders affecting HDL-C levels in humans provide conflicting data about HDL being antiatherogenic. This review addresses the current state of knowledge regarding HDL based on these recent controversies.

摘要

流行病学研究表明,血浆高密度脂蛋白胆固醇(HDL-C)浓度与心血管疾病(CVD)发病率呈负相关。HDL的抗动脉粥样硬化作用不仅归因于其抗炎、抗血栓形成和抗氧化特性,还归因于其参与逆向胆固醇转运(RCT),即外周组织(包括动脉内膜巨噬细胞)中的胆固醇被输送到肝脏以便通过胆汁排泄。由于这些作用,HDL-C已成为预防CVD的一个有吸引力的靶点。然而,托彻普(一种能大幅提高HDL-C水平的药物)在预防CVD方面的失败,以及动物模型研究和影响人类HDL-C水平的单基因疾病携带者的研究数据,提供了关于HDL是否具有抗动脉粥样硬化作用的相互矛盾的数据。本综述基于这些近期的争议探讨了关于HDL的当前知识状态。

相似文献

1
[HDL: the yin-yang of cardiovascular disease].[高密度脂蛋白:心血管疾病的阴阳两面]
Arq Bras Endocrinol Metabol. 2010 Dec;54(9):777-84. doi: 10.1590/s0004-27302010000900002.
2
Implications of torcetrapib failure for the future of HDL therapy: is HDL-cholesterol the right target?托彻普失败对高密度脂蛋白治疗未来的启示:高密度脂蛋白胆固醇是正确的靶点吗?
Expert Rev Cardiovasc Ther. 2010 Mar;8(3):345-58. doi: 10.1586/erc.10.6.
3
High-Density Lipoprotein Processing and Premature Cardiovascular Disease.高密度脂蛋白代谢与心血管疾病早发
Methodist Debakey Cardiovasc J. 2015 Jul-Sep;11(3):181-5. doi: 10.14797/mdcj-11-3-181.
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Cholesterol efflux and reverse cholesterol transport.胆固醇流出与胆固醇逆向转运。
Handb Exp Pharmacol. 2015;224:181-206. doi: 10.1007/978-3-319-09665-0_4.
5
The failure of torcetrapib: was it the molecule or the mechanism?托彻普的失败:是药物分子的问题还是作用机制的问题?
Arterioscler Thromb Vasc Biol. 2007 Feb;27(2):257-60. doi: 10.1161/01.ATV.0000256728.60226.77.
6
Inhibition of cholesteryl ester transfer protein by torcetrapib modestly increases macrophage cholesterol efflux to HDL.托彻普(torcetrapib)对胆固醇酯转运蛋白的抑制作用适度增加了巨噬细胞向高密度脂蛋白的胆固醇外流。
Arterioscler Thromb Vasc Biol. 2007 May;27(5):1132-8. doi: 10.1161/ATVBAHA.106.138347. Epub 2007 Feb 22.
7
Dissociating HDL cholesterol from cardiovascular risk.将高密度脂蛋白胆固醇与心血管风险分离开来。
Lancet. 2010 Jul 31;376(9738):305-6. doi: 10.1016/S0140-6736(10)61021-5. Epub 2010 Jul 23.
8
Advances in the Study of the Antiatherogenic Function and Novel Therapies for HDL.高密度脂蛋白的抗动脉粥样硬化功能及新型疗法的研究进展
Int J Mol Sci. 2015 Jul 28;16(8):17245-72. doi: 10.3390/ijms160817245.
9
Targeting residual cardiovascular risk: raising high-density lipoprotein cholesterol levels.针对残余心血管风险:提高高密度脂蛋白胆固醇水平。
Heart. 2008 Jun;94(6):706-14. doi: 10.1136/hrt.2007.125401.
10
Effect of torcetrapib on the progression of coronary atherosclerosis.托彻普对冠状动脉粥样硬化进展的影响。
N Engl J Med. 2007 Mar 29;356(13):1304-16. doi: 10.1056/NEJMoa070635. Epub 2007 Mar 26.

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