Sleep Disturbance and HMG CoA Reductase Inhibitors
- 5 September 1990
- journal article
- research article
- Published by American Medical Association (AMA) in JAMA
- Vol. 264 (9), 1105
- https://doi.org/10.1001/jama.1990.03450090041020
Abstract
To the Editor.— The National Cholesterol Education Program's treatment guidelines1have led to a substantial increase in the treatment of hypercholesterolemia. Lovastatin (Mevacor) was approved by the Food and Drug Administration in 1987 and is now the most frequently prescribed hypolipidemic agent.2The recognized adverse effects of lovastatin have been mainly confined to reversible liver transaminase elevations and, rarely, myopathy.3 Schaefer4 reported that nine (17.6%) of 51 patients taking lovastatin by prescription had decreased sleep of 1 to 3 hours, compared with none of 33 patients receiving another 3-hydroxy-3-methylglutaryl coenzyme A (HMG CoA) reductase inhibitor, pravastatin, in a clinical trial. Study.— We have assessed the prevalence of sleep disorders more systematically, using a standard questionnaire, in 409 hyperlipidemic patients (67% male) being treated by diet alone (n=102), receiving three different types of HMG CoA reductase inhibitor (lovastatin [n = 161], simvastatin [n = 47], and pravastatin [n = 45]), orKeywords
This publication has 3 references indexed in Scilit:
- Clinical experience with lovastatinThe American Journal of Cardiology, 1990
- The Diagnosis and Management of InsomniaNew England Journal of Medicine, 1990
- A scale for the estimation of sleep problems in clinical researchJournal of Clinical Epidemiology, 1988