Clark Luther T
Division of Cardiovascular Medicine, State University of New York Downstate Medical Center, Brooklyn, New York 11203-2098, USA.
Clin Cardiol. 2004 Jun;27(6 Suppl 3):III22-6. doi: 10.1002/clc.4960271507.
The efficacy of statins in lowering low-density lipoprotein cholesterol (LDL-C) and reducing coronary heart disease risk is well established; however, recent evidence suggests that more aggressive lipid management, even beyond achievement of currently recommended LDL-C goals, may provide additional clinical benefits. A novel approach to the aggressive lowering of LDL-C is the combination of statins with agents that affect different aspects of cholesterol metabolism. Because absorption of cholesterol is an important contributor to cholesterol balance, the simultaneous inhibition of cholesterol absorption and cholesterol synthesis is an attractive approach to achieving greater LDL-C reductions. In clinical trials, the combination of the cholesterol absorption inhibitor ezetimibe with a statin resulted in greater improvements in lipids than statin monotherapy and allowed a greater percentage of patients to achieve treatment goals. In addition, this combination may offer benefits through reduction of phytosterols, chylomicron remnants, and C-reactive protein. Several ongoing trials are evaluating whether the benefit of simultaneously blocking cholesterol synthesis and intestinal cholesterol absorption translates into better clinical outcomes.
他汀类药物在降低低密度脂蛋白胆固醇(LDL-C)和降低冠心病风险方面的疗效已得到充分证实;然而,最近的证据表明,更积极的血脂管理,甚至超出目前推荐的LDL-C目标的实现,可能会带来额外的临床益处。一种积极降低LDL-C的新方法是将他汀类药物与影响胆固醇代谢不同方面的药物联合使用。由于胆固醇吸收是胆固醇平衡的一个重要因素,同时抑制胆固醇吸收和胆固醇合成是实现更大程度降低LDL-C的一种有吸引力的方法。在临床试验中,胆固醇吸收抑制剂依泽替米贝与他汀类药物联合使用比他汀类药物单药治疗能更有效地改善血脂,并使更多患者达到治疗目标。此外,这种联合用药可能通过降低植物甾醇、乳糜微粒残粒和C反应蛋白而带来益处。几项正在进行的试验正在评估同时阻断胆固醇合成和肠道胆固醇吸收的益处是否能转化为更好的临床结果。