Rosenson Robert S
Preventive Cardiology Center, Northwestern University, The Feinberg School of Medicine, Chicago, Illinois 60611, USA.
Am J Med. 2004 Mar 15;116(6):408-16. doi: 10.1016/j.amjmed.2003.10.033.
Statins are an efficacious and well-tolerated class of lipid-altering agents that have been shown to reduce the risk of initial and recurrent cardiovascular events. However, cerivastatin was withdrawn from the world market because of its potential for severe myotoxic effects. Since the benefits of statin treatment outweigh the small risk of adverse events, statins remain the first-line therapy for lipid lowering and preventing atherosclerotic cardiovascular diseases. The risk of myopathy may be minimized with the appropriate choice of agent and by identifying patients at risk of myotoxic effects. Elderly or female patients, or those with concomitant medications or impaired metabolic processes, may be at increased risk and should be monitored closely. The risk of myopathy may also be inferred from the pharmacologic and pharmacokinetic properties of the statin used. Since myotoxic events are more frequent at higher doses, statins that are effective in reducing cholesterol levels and helping patients to reach target levels at start doses may be useful. The lipophilicity of a statin and its potential for drug-drug interactions may also help to determine the likelihood of muscular effects. Drug-drug interactions may be avoided by selecting a statin that does not share the same metabolic pathway.
他汀类药物是一类有效且耐受性良好的调脂药物,已被证明可降低首次及复发性心血管事件的风险。然而,西立伐他汀因具有严重的肌毒性作用而退出全球市场。由于他汀类药物治疗的益处大于不良事件的小风险,他汀类药物仍然是降脂和预防动脉粥样硬化性心血管疾病的一线治疗药物。通过适当选择药物并识别有肌毒性作用风险的患者,可将肌病风险降至最低。老年或女性患者,或那些同时服用其他药物或代谢过程受损的患者,可能风险增加,应密切监测。肌病风险也可从所用他汀类药物的药理和药代动力学特性推断出来。由于高剂量时肌毒性事件更频繁,在起始剂量时能有效降低胆固醇水平并帮助患者达到目标水平的他汀类药物可能是有用的。他汀类药物的亲脂性及其药物相互作用的可能性也可能有助于确定肌肉效应的可能性。通过选择不共享相同代谢途径的他汀类药物可避免药物相互作用。