No conflict of interest was declared.
Original Report
Exploring the risk of diabetes mellitus and dyslipidemia among ambulatory users of atypical antipsychotics: a population-based comparison of risperidone and olanzapine†
Article first published online: 22 MAR 2005
DOI: 10.1002/pds.1093
Copyright © 2005 John Wiley & Sons, Ltd.
Additional Information
How to Cite
Moisan, J., Grégoire, J.-P., Gaudet, M. and Cooper, D. (2005), Exploring the risk of diabetes mellitus and dyslipidemia among ambulatory users of atypical antipsychotics: a population-based comparison of risperidone and olanzapine. Pharmacoepidemiology and Drug Safety, 14: 427–436. doi: 10.1002/pds.1093
- †
Publication History
- Issue published online: 27 MAY 2005
- Article first published online: 22 MAR 2005
- Manuscript Accepted: 20 DEC 2004
- Manuscript Revised: 6 DEC 2004
- Manuscript Received: 15 APR 2004
Funded by
- Janssen-Ortho, Inc.
- Abstract
- References
- Cited By
Keywords:
- diabetes mellitus;
- dyslipidemia;
- atypical antipsychotics;
- population-based;
- cohort study
Abstract
Purpose
To compare the incidence rates of diabetes mellitus and dyslipidemia in ambulatory first-time users of risperidone and olanzapine.
Methods
The database for the Prescription Drug Insurance Plan in the province of Quebec was used as the data source for a population-based cohort study. Denominalized data were extracted for all ambulatory patients who first received an atypical antipsychotic between 1 January 1997 and 31 August 1999. Eligible patients were categorized as taking: no antidiabetic medication; no lipid reducing medication; neither type of medication. Those who started to use an outcome drug (an antidiabetic or lipid-lowering medication) before the end of the follow-up period (31 August 2000) were considered to have developed the corresponding outcome disease. Incidence rate ratios (IRR) (and 95% confidence intervals) for initiating antihyperglycemic or lipid-lowering drug treatment, or both were calculated. Outcomes on risperidone were compared to those on olanzapine.
Results
A total of 19 582 eligible patients were included in the analysis. Relative to risperidone, olanzapine was associated with a higher risk of initiating a pharmacologic treatment for diabetes [IRR: 1.33 (1.03–1.74)], dyslipidemia [IRR: 1.49 (1.22–1.83)], or either condition [1.47 (1.23–1.76)].
Conclusions
Olanzapine seems to be associated with a higher risk of developing diabetes and/or dyslipidemia than risperidone. Further prospective studies are needed to rigorously assess the safety of olanzapine. Copyright © 2005 John Wiley & Sons, Ltd.

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