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达塞曲匹,胆固醇酯转移蛋白调节剂。

Dalcetrapib , a cholesteryl ester transfer protein modulator.

机构信息

Royal Perth Hospital, Department of Core Clinical Pathology & Biochemistry, PathWest Laboratory Medicine WA, Perth, Western Australia.

出版信息

Expert Opin Investig Drugs. 2012 Sep;21(9):1427-32. doi: 10.1517/13543784.2012.699040. Epub 2012 Jun 24.

DOI:10.1517/13543784.2012.699040
PMID:22725099
Abstract

INTRODUCTION

Cholesteryl ester transfer protein (CETP) plays an important role in reverse cholesterol transport by transferring cholesteryl esters from high-density lipoprotein (HDL) to the apolipoprotein B-containing lipoproteins. Inhibition of CETP is a target to increase HDL-cholesterol and potentially reduce atherosclerosis. Dalcetrapib is an orally administered CETP inhibitor developed for the treatment of primary hypercholesterolaemia and mixed hyperlipidaemia.

AREAS COVERED

AREAS COVERED are: mode of action, preclinical development and clinical trials of dalcetrapib, a CETP modulator. The article provides an understanding of the pharmacokinetic and pharmacodynamic characteristics of dalcetrapib and insight into its clinical efficacy and safety. In clinical trials, dalcetrapib produced significant elevations in HDL-cholesterol when taken alone or in combination with statin with no effect on blood pressure or expression of genes involved in the renin-angiotensin-aldosterone system.

EXPERT OPINION

Although dalcetrapib is the least potent CETP inhibitor, it does not impair the formation of CETP-induced pre-β HDL, which might be needed to increase reverse cholesterol transport. While dalcetrapib is well-tolerated and does not show major side effects, the recent interim results of the Phase III dal-OUTCOMES trial have shown the lack of a clinically meaningful benefit, and further testing of the drug has been halted.

摘要

简介

胆固醇酯转移蛋白(CETP)在胆固醇逆转运中发挥重要作用,可将胆固醇酯从高密度脂蛋白(HDL)转移到载脂蛋白 B 脂蛋白。CETP 抑制剂是增加 HDL-胆固醇并可能减少动脉粥样硬化的靶点。达塞曲匹是一种口服 CETP 抑制剂,用于治疗原发性高胆固醇血症和混合性高脂血症。

涵盖领域

涵盖领域包括:CETP 调节剂达塞曲匹的作用机制、临床前开发和临床试验。本文介绍了达塞曲匹的药代动力学和药效学特征,并深入了解了其临床疗效和安全性。在临床试验中,达塞曲匹单独使用或与他汀类药物联合使用时,可显著升高 HDL-胆固醇,对血压或肾素-血管紧张素-醛固酮系统相关基因的表达无影响。

专家意见

虽然达塞曲匹是 CETP 抑制剂中活性最低的,但它不会损害 CETP 诱导的前-β HDL 的形成,这可能是增加胆固醇逆转运所必需的。达塞曲匹耐受性良好,没有出现主要副作用,但最近 III 期 dal-OUTCOMES 试验的中期结果显示,该药物没有带来有临床意义的益处,进一步的药物测试已经停止。

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