Davidson Michael H
Chicago Center for Clinical Research, IL 60610-4324, USA.
Expert Rev Cardiovasc Ther. 2003 May;1(1):11-21. doi: 10.1586/14779072.1.1.11.
Elevated low-density lipoprotein (LDL)-cholesterol is associated with a significantly increased risk of coronary heart disease but lowering LDL-cholesterol to levels established in current National Cholesterol Education Program (NCEP) guidelines provides significant risk reduction. Nevertheless, many patients receiving lipid-lowering therapy, particularly those at highest coronary heart disease risk, do not reach LDL-cholesterol goals with their current medications. Ezetimibe (Zetia, Merck Schering-Plough) is the first of a new class of lipid-lowering drugs known as cholesterol absorption inhibitors. Ezetimibe has a favorable pharmacokinetic profile, which allows it to be administered once daily and to be given in conjunction with statins. In a series of randomized, controlled, multicenter studies, ezetimibe produced significant improvements in levels of LDL-cholesterol and other lipid parameters when used as monotherapy, with a safety profile comparable with that of placebo. Furthermore, coadministration of ezetimibe with a statin (simvastatin, atorvastatin, lovastatin, or pravastatin) was more effective than statin monotherapy in lowering LDL-cholesterol and improving other lipid parameters. Moreover, coadministration of ezetimibe with a statin allowed a greater percentage of patients to achieve treatment goals established in NCEP guidelines. The safety and side-effect profile of ezetimibe plus statin coadministration therapy was generally comparable with that of statin monotherapy. These studies establish ezetimibe as an effective lipid-lowering agent, which will likely be useful in the management of a broad range of patients with hypercholesterolemia. Ezetimibe can be used in conjunction with a statin at the beginning of therapy, or it can be added if patients do not achieve their LDL-cholesterol goal with statins alone.
低密度脂蛋白(LDL)胆固醇升高与冠心病风险显著增加相关,但将LDL胆固醇降至现行国家胆固醇教育计划(NCEP)指南所确定的水平可显著降低风险。然而,许多接受降脂治疗的患者,尤其是那些冠心病风险最高的患者,目前使用的药物无法使LDL胆固醇达到目标值。依折麦布(益适纯,默克雪兰诺)是一类新型降脂药物(称为胆固醇吸收抑制剂)中的首个药物。依折麦布具有良好的药代动力学特性,允许每日给药一次,并可与他汀类药物联合使用。在一系列随机、对照、多中心研究中,依折麦布作为单一疗法使用时,可使LDL胆固醇水平及其他血脂参数显著改善,其安全性与安慰剂相当。此外,依折麦布与他汀类药物(辛伐他汀、阿托伐他汀、洛伐他汀或普伐他汀)联合使用在降低LDL胆固醇及改善其他血脂参数方面比他汀类药物单一疗法更有效。而且,依折麦布与他汀类药物联合使用可使更大比例的患者达到NCEP指南所确定的治疗目标。依折麦布加他汀联合治疗的安全性和副作用情况总体上与他汀类药物单一疗法相当。这些研究确立了依折麦布作为一种有效的降脂药物,可能对广泛的高胆固醇血症患者的管理有用。依折麦布可在治疗开始时与他汀类药物联合使用,或者如果患者仅使用他汀类药物未达到LDL胆固醇目标,也可加用依折麦布。