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Volume 60, Issue 8, Pages 812-818 (August 2007)


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Statin and statin–fibrate use was significantly associated with increased myositis risk in a managed care population

David L. McClureaCorresponding Author Informationemail address, Robert J. Valuckb, Morton Glanzc, James R. Murphyd, John E. Hokansone

Accepted 7 November 2006. published online 24 March 2007.

Abstract 

Objective

We quantified the risk of myositis associated with statin and fibrate drug use with other covariates within a managed care organization (MCO) population.

Study Design and Setting

The study spanned the years 1999–2003. Myositis cases had creatine kinase (CK) ≥10× upper limit of normal and a myopathy diagnosis. Exposures of statins, fibrates, and other drugs were assessed with age, gender, and indicators of suspected myopathy risk. Exposures were first analyzed within a cohort with CK monitoring and then within a more general secondary cohort. Adjusted relative risks (RRs) and incidence rates of myositis were generated by Poisson regression.

Results

Myositis was significantly associated with statin monotherapy (RR 2.8 [95% confidence interval, CI=1.3–5.9]), statin–fibrate combination therapy (9.1 [95% CI=3.5–23]), comorbid liver disease (4.3 [95% CI=1.5–13], and/or renal disease (2.5 [95% CI=1.3–5.0]). Myositis rates per covariate pattern ranged from 33 to 6,400 per 100,000 person-years. The mean time to event was 1.7 years for statin–fibrate use, 2.0 years for statins alone, and 2.1 years for unexposed. Within the secondary cohort, RRs increased up to 10 times further away from the null.

Conclusion

Statins, with or without fibrates, and liver and renal disease were significantly associated with increased myositis risk in an MCO population.

a Clinical Research Unit, Kaiser Permanente Colorado, Denver, CO 80237-8066, USA

b Department of Clinical Pharmacy, University of Colorado Health Sciences Center, Denver, CO 80262, USA

c Harvard Medical School, Boston, MA 02115, USA

d Division of Biostatistics, National Jewish Medical and Research Center, Denver, CO 80206, USA

e Department of Preventive Medicine and Biostatistics, University of Colorado Health Sciences Center, Denver, CO 80262, USA

Corresponding Author InformationCorresponding author. Kaiser Permanente Colorado, P.O. Box 378066, Denver, Colorado 80237-8066, USA. Tel.: +1-303-614-1255; fax: +1-303-614-1255.

PII: S0895-4356(06)00432-X

doi:10.1016/j.jclinepi.2006.11.006


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