Statin Intolerance: an Overview of US and International Guidance

Curr Atheroscler Rep. 2023 Aug;25(8):517-526. doi: 10.1007/s11883-023-01124-z. Epub 2023 Jul 6.

Abstract

Purpose of review: To review recent international and domestic definitions, considerations, and treatment algorithms for statin intolerance, and specifically, statin-associated muscle symptoms (SAMS).

Recent findings: Multiple organizations around the world have produced guidance documents to aid clinicians on managing statin intolerance. A common theme resides among all the guidance documents that most patients can tolerate statins. For those patients who cannot, healthcare teams need to evaluate, rechallenge, educate, and ensure adequate reduction of atherogenic lipoproteins. Statin therapy remains the cornerstone of lipid-lowering therapies to reduce atherosclerotic cardiovascular disease (ASCVD) and reduce mortality and morbidity. The common theme throughout all these guidance documents is the importance of statin therapy to reduce ASCVD and continual adherence to treatment. Because adverse events occur and inhibit patients from achieving adequate lowering of their atherogenic lipoproteins, trial and rechallenge of statin therapy, as well as addition of non-statin therapies, especially in high-risk patients, is also undisputed. The main differences stem from laboratory monitoring and the classification of the severity of the adverse effect. Future research should focus on consistently diagnosing SAMS so that these patients can be easily identified in the electronic health records.

Keywords: Adherence; Cholesterol; Non-statin; Persistence; Statin; Statin intolerance.

Publication types

  • Review
  • Research Support, N.I.H., Extramural

MeSH terms

  • Atherosclerosis* / drug therapy
  • Cardiovascular Diseases* / chemically induced
  • Cardiovascular Diseases* / drug therapy
  • Cardiovascular Diseases* / prevention & control
  • Humans
  • Hydroxymethylglutaryl-CoA Reductase Inhibitors* / adverse effects
  • Lipoproteins

Substances

  • Hydroxymethylglutaryl-CoA Reductase Inhibitors
  • Lipoproteins