Daskalopoulou Stella S, Mikhailidis Dimitri P
Department of Clinical Biochemistry, Royal Free Hospital, Royal Free and University College School of Medicine, London NW3 2QG, UK.
Curr Med Res Opin. 2006 Mar;22(3):511-28. doi: 10.1185/030079906X89856.
Lowering serum cholesterol levels reduces the risk of coronary heart disease (CHD)-related events. Statins are commonly prescribed as first-line treatment but many patients at high-risk for CHD still fail to reach their cholesterol or low-density lipoprotein cholesterol (LDL-C) goals with statin monotherapy. National and international guidelines for the prevention of CHD recommend the modification of lipid profiles and particularly LDL-C [e.g. the National Cholesterol Education Program Adult Treatment Panel III (NCEP ATP III; 2001) and Third Joint Task Force of European and other Societies on Cardiovascular Disease Prevention in Clinical Practice (2003) Guidelines]. Several recent clinical trials indicated an added benefit from aggressive lowering of LDL-C levels. Based on these findings, the NCEP ATP III revised the LDL-C target from < 100 mg/dL (2.6 mmol/L) to < 70 mg/dL (1.8 mmol/L) (optional target) for very high-risk patients and < 130 mg/dL (3.4 mmol/L) to < 100 mg/dL (2.6 mmol/L) for moderately high-risk patients. For patients who fail to achieve their LDL-C target, inhibiting the two main sources of cholesterol - synthesis and uptake - can produce more effective lipid lowering, allowing more patients to reach their LDL-C goal. Ezetimibe is a highly-selective inhibitor of cholesterol absorption and simvastatin is an evidence-based inhibitor of cholesterol synthesis. The LDL-C-lowering efficacy of targeting both major sources of cholesterol with ezetimibe plus simvastatin was demonstrated in several multicentre, double-blind, placebo-controlled trials in patients with hypercholesterolaemia. For patients who do not reach their cholesterol goal with a statin, adding ezetimibe 10 mg significantly reduces LDL-C compared with statin monotherapy. Thus, this treatment option may help patients reach the new 'stricter' cholesterol goals. This review, based on a Medline database search from January 2000 to August 2005, considers the LDL-C-lowering efficacy of ezetimibe and discusses the role of this agent for patients who fail to achieve guideline cholesterol goals with statin monotherapy.
降低血清胆固醇水平可降低冠心病(CHD)相关事件的风险。他汀类药物通常被作为一线治疗药物,但许多冠心病高危患者采用他汀类药物单药治疗仍无法达到其胆固醇或低密度脂蛋白胆固醇(LDL-C)目标。国家和国际上预防冠心病的指南推荐改善血脂谱,尤其是LDL-C [例如美国国家胆固醇教育计划成人治疗专家组第三次报告(NCEP ATP III;2001年)以及欧洲和其他学会关于临床实践中心血管疾病预防的第三次联合工作组(2003年)指南]。最近的几项临床试验表明积极降低LDL-C水平有额外益处。基于这些研究结果,NCEP ATP III将极高危患者的LDL-C目标从<100 mg/dL(2.6 mmol/L)修订为<70 mg/dL(1.8 mmol/L)(可选目标),将中高危患者的LDL-C目标从<130 mg/dL(3.4 mmol/L)修订为<100 mg/dL(2.6 mmol/L)。对于未达到LDL-C目标的患者,抑制胆固醇的两个主要来源——合成和摄取——可更有效地降低血脂,使更多患者达到LDL-C目标。依折麦布是一种高选择性胆固醇吸收抑制剂,辛伐他汀是一种经循证的胆固醇合成抑制剂。在多项针对高胆固醇血症患者的多中心、双盲、安慰剂对照试验中证实了依折麦布加辛伐他汀针对胆固醇的两个主要来源进行治疗降低LDL-C的疗效。对于使用他汀类药物未达到胆固醇目标的患者,加用10 mg依折麦布与他汀类药物单药治疗相比可显著降低LDL-C。因此,这种治疗方案可能有助于患者达到新的“更严格”的胆固醇目标。本综述基于2000年1月至2005年8月对Medline数据库的检索,探讨了依折麦布降低LDL-C的疗效,并讨论了该药物在他汀类药物单药治疗未达到指南规定胆固醇目标的患者中的作用。