Wortmann Robert L
Department of Internal Medicine, The University of Oklahoma College of Medicine, Tulsa, 74135-2512, USA.
Curr Opin Rheumatol. 2002 Nov;14(6):643-7. doi: 10.1097/00002281-200211000-00002.
Each of the lipid-lowering agents available today can cause myopathy. The severity of the muscle disorder may vary from trivial myalgias or elevations of creatine kinase in asymptomatic individuals to rhabdomyolysis with myoglobinuria, renal failure, and death. Fortunately, significant myopathy occurs at a low rate. However, the large number of individuals taking these medications renders it a significant problem. Although the pathophysiology of the myopathy remains speculative, its occurrence appears to be dose related. Consequently, the total dosage of lipid-lowering drug consumed, the concomitant use of other medications that affect their blood levels, and the individual's specific drug-metabolizing enzyme profile may contribute to this toxicity.
如今可用的每种降脂药物都可能导致肌病。肌肉疾病的严重程度差异很大,从无症状个体的轻微肌痛或肌酸激酶升高到伴有肌红蛋白尿、肾衰竭和死亡的横纹肌溶解症。幸运的是,严重肌病的发生率很低。然而,服用这些药物的人数众多,使其成为一个重大问题。虽然肌病的病理生理学仍属推测,但它的发生似乎与剂量有关。因此,所消耗的降脂药物的总剂量、影响其血药浓度的其他药物的同时使用,以及个体特定的药物代谢酶谱可能导致这种毒性。