Roten Laurent, Schoenenberger Ronald A, Krähenbühl Stephan, Schlienger Raymond G
Department of Internal Medicine, Bürgerspital, Solothurn, Switzerland.
Ann Pharmacother. 2004 Jun;38(6):978-81. doi: 10.1345/aph.1D498. Epub 2004 Apr 6.
To report a case of severe myopathy associated with concomitant simvastatin and amiodarone therapy.
A 63-year-old white man with underlying insulin-dependent diabetes, recent coronary artery bypass surgery, and postoperative hemiplegia was treated with aspirin, metoprolol, furosemide, nitroglycerin, and simvastatin. Due to recurrent atrial fibrillation, oral anticoagulation with phenprocoumon and antiarrhythmic treatment with amiodarone were initiated. Four weeks after starting simvastatin 40 mg/day and 2 weeks after initiating amiodarone 1 g/day for 10 days, then 200 mg/day, he developed diffuse muscle pain with generalized muscular weakness. Laboratory investigations revealed a significant increase of creatine kinase (CK) peaking at 40 392 U/L. Due to a suspected drug interaction of simvastatin with amiodarone, both drugs were stopped. CK normalized over the following 8 days, and the patient made an uneventful recovery. An objective causality assessment revealed that the myopathy was probably related to simvastatin.
Myopathy is a rare but potentially severe adverse reaction associated with statins. Besides high statin doses, concomitant use of fibrates, defined comorbidities, and concurrent use of inhibitors of cytochrome P450 are important additional risk factors. This is especially relevant if statins predominantly metabolized by CYP3A4 are combined with inhibitors of this isoenzyme. Amiodarone is a potent inhibitor of several different CYP isoenzymes, including CYP3A4.
Avoiding the concomitant use of drugs with the potential to inhibit CYP-dependent metabolism (eg, amiodarone) or elimination of statins may decrease the risk of statin-associated myopathy. Alternatively, if drug therapy with a potent CYP inhibitor is inevitable, choosing a statin without relevant CYP metabolism (eg, pravastatin) should be considered.
报告1例与辛伐他汀和胺碘酮联合治疗相关的严重肌病病例。
一名63岁白人男性,患有胰岛素依赖型糖尿病、近期接受冠状动脉搭桥手术且术后偏瘫,接受阿司匹林、美托洛尔、呋塞米、硝酸甘油和辛伐他汀治疗。由于反复出现心房颤动,开始使用苯丙香豆素进行口服抗凝治疗,并使用胺碘酮进行抗心律失常治疗。在开始每天服用40mg辛伐他汀4周后,以及开始每天服用1g胺碘酮10天然后每天服用200mg 2周后,他出现了弥漫性肌肉疼痛和全身肌肉无力。实验室检查显示肌酸激酶(CK)显著升高,峰值达到40392U/L。由于怀疑辛伐他汀与胺碘酮存在药物相互作用,两种药物均停用。CK在接下来的8天内恢复正常,患者顺利康复。客观因果关系评估显示,肌病可能与辛伐他汀有关。
肌病是与他汀类药物相关的一种罕见但可能严重的不良反应。除了高剂量他汀类药物外,贝特类药物的联合使用、特定的合并症以及细胞色素P450抑制剂的同时使用是重要的额外危险因素。如果主要由CYP3A4代谢的他汀类药物与该同工酶的抑制剂联合使用,这一点尤为重要。胺碘酮是几种不同CYP同工酶的强效抑制剂,包括CYP3A4。
避免同时使用具有抑制CYP依赖性代谢潜力的药物(如胺碘酮)或停用他汀类药物可能会降低他汀类药物相关肌病的风险。或者,如果不可避免地要使用强效CYP抑制剂进行药物治疗,则应考虑选择无相关CYP代谢的他汀类药物(如普伐他汀)。