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Myotoxicity associated with lipid-lowering drugs.

机译:与降脂药有关的肌毒性。

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PURPOSE OF REVIEW: Lipid-lowering drugs are associated with myotoxicity, which ranges in severity from myalgias to rhabdomyolysis resulting in renal failure and death. Although rhabdomyolysis is rare, muscle symptoms and serum creatine kinase elevations are sufficiently frequent during the course of lipid-lowering drug therapy to pose diagnostic challenges for the clinician. Progress in our understanding of this form of myotoxicity is reviewed. RECENT FINDINGS: Muscle pain and weakness are the cardinal symptoms and often interfere with vigorous exercise. These symptoms may occur with or without serum creatine kinase elevations. The risk of myotoxicity is increased by combination statin-fibrate therapy as well as by factors that elevate tissue levels of the lipid-lowering drug, including the dose, drug-drug interactions, and host factors. Underlying neuromuscular diseases may become clinically apparent during statin therapy and may predispose to myotoxicity. The pathophysiology of myotoxicity most probably involves metabolic effects of the statins on the isoprenoid pool and on mitochondrial function. SUMMARY: Management of myotoxicity requires an evaluation of risk factors prior to prescribing lipid-lowering drugs, attention to muscle symptoms, and withdrawal of drug in the event of significant abnormalities.
机译:审查目的:降血脂药物与肌毒性有关,其严重程度从肌痛到横纹肌溶解,导致肾功能衰竭和死亡。尽管横纹肌溶解很少见,但在降脂药物治疗过程中肌肉症状和血清肌酸激酶升高足够频繁,给临床医生带来了诊断挑战。综述了我们对这种形式的肌毒性的理解的进展。最近的发现:肌肉疼痛和无力是主要症状,通常会干扰剧烈运动。这些症状可能在血清肌酸激酶升高或不升高的情况下发生。他汀类药物联合贝特类药物治疗以及升高降脂药物组织水平的因素(包括剂量,药物相互作用和宿主因素)会增加肌毒性的风险。在他汀类药物治疗期间,潜在的神经肌肉疾病在临床上可能会变得很明显,并且容易诱发肌毒性。肌毒性的病理生理学最可能涉及他汀类药物对类异戊二烯库和线粒体功能的代谢作用。总结:肌毒性的治疗需要在开降脂药,评估肌肉症状以及在出现明显异常事件时停药之前评估危险因素。

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