4.7 Review

Narrative Review: Statin-Related Myopathy

期刊

ANNALS OF INTERNAL MEDICINE
卷 150, 期 12, 页码 858-U63

出版社

AMER COLL PHYSICIANS
DOI: 10.7326/0003-4819-150-12-200906160-00009

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资金

  1. Heart and Stroke Foundation of Ontario [CI-5710, PRG-5967, NA-Review 6059, T-6018]
  2. Canadian Institutes for Health Research [MOP-13430, MOP-39533, MOP-39833]
  3. Ontario Research Fund
  4. Ontario Genomics Institute

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Statin-related myopathy is a clinically important cause of statin intolerance and discontinuation. The spectrum of statin-related myopathy ranges from common but clinically benign myalgia to rare but life-threatening rhabdomyolysis. Observational studies suggest that myalgia can occur in up to 10% of persons prescribed statins, whereas rhabdomyolysis continues to be rare. The mechanisms of statin-related myopathy are unclear. Options for managing statin myopathy include statin switching, particularly to fluvastatin or low-dose rosuvastatin; nondaily dosing regimens; nonstatin alternatives, such as ezetimibe and bile acid-binding resins; and coenzyme Q10 supplementation. Few of these strategies have high-quality evidence supporting them. Because statin-related myopathy will probably become more common with greater numbers of persons starting high-dose statin therapy and the increasing stringency of low-density lipoprotein cholesterol level targets, research to better identify patients at risk for statin myopathy and to evaluate management strategies for statin-related myopathy is warranted.

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