Effects of Switching From Olanzapine, Quetiapine, and Risperidone to Aripiprazole on 10-Year Coronary Heart Disease Risk and Metabolic Syndrome Status: Results From a Randomized Controlled Trial
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Purpose This study examined the clinical significance of switching from olanzapine, quetiapine, or risperidone to aripiprazole by examining changes in predicted risk of cardiovascular disease (CVD) according to the Framingham Risk Score (FRS) and metabolic syndrome status. FRS estimates 10-year risk of "hard" coronary heart disease (CHD) outcomes (myocardial infarction and coronary death) while metabolic syndrome is associated with increased risk of CVD, stroke, and diabetes mellitus. Method Changes in FRS and metabolic syndrome status were compared between patients with BMI ≥ 27 and non-HDL-C ≥ 130 mg/dL randomly assigned to stay on stable current treatment (olanzapine, quetiapine, or risperidone) or switch to treatment with aripiprazole with 24 weeks of follow-up. All study participants were enrolled in a behavioral program that promoted healthy diet and exercise. Results The pre-specified analyses included 89 switchers and 98 stayers who had post-baseline measurements needed to assess changes. Least squares mean estimates of 10-year CHD risk decreased more for the switch (from 7.0% to 5.2%) than the stay group (from 7.4% to 6.4%) (p = 0.0429). The odds ratio for having metabolic syndrome (stay vs. switch) at the last observation was 1.748 (95% CI 0.919, 3.324, p = 0.0885). Conclusion Switching from olanzapine, quetiapine, or risperidone to aripiprazole was associated with larger reductions in predicted 10-year risk of CHD than the behavioral program alone. The advantage of switching on metabolic syndrome was not statistically significant. The benefits of switching must be balanced against its risks, which in this study included more discontinuations of the study treatment but no significant increase in symptoms or hospitalizations.
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Many of the studies reporting on the effect of switching to partial agonists were uncontrolled with metabolic disturbances being the primary outcome, which increases the risk that participants engaged in parallel weight reducing behaviors, which could inflate the effect.
“Many of the studies reporting on the effect of switching to partial agonists were uncontrolled with metabolic disturbances being the primary outcome, which increases the risk that the participants engaged in parallel weight reducing behaviors, seen as a manualized co-treatment in one study (77), which could inflate the effect.”
From Reversibility of Antipsychotic-Induced Weight Gain: A Systematic Review and Meta-Analysis (2021) · cites this paper as [77]
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Correll, C. U., Detraux, J., De Lepeleire, J., & De Hert, M. (2015) · World Psychiatry · doi:10.1002/wps.20204 · Cited by 820 · see citing works
Reversibility of Antipsychotic-Induced Weight Gain: A Systematic Review and Meta-Analysis
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- Authors
- Stroup, T. S., Byerly, M. J., Nasrallah, H. A., Ray, N., Khan, A. Y., Lamberti, J. S., Glick, I. D., Steinbook, R. M., McEvoy, J. P., & Hamer, R. M.
- Affiliations
- New York State Psychiatric Institute (US)
- The University of Texas Southwestern Medical Center (US)
- University of Cincinnati (US)
- University of North Carolina at Chapel Hill (US)
- University of Rochester (US)
- Stanford University (US)
- University of Miami (US)
- Duke Medical Center (US)
- Corresponding author
- Stroup, T. Scott
- Venue
- Schizophrenia Research
- Publisher
- Elsevier BV
- Published
- 2013-05
- Volume
- 146
- Issue
- 1-3
- Pages
- 190-195
- ISSN
- 0920-9964 (ISSN-L)
- PMC
- PMC3622801
- OpenAlex
- W2063649818
- Cited by
- 39
- References
- 3
- Citations by year
- 2026: 2 · 2025: 4 · 2024: 2 · 2023: 1 · 2022: 3 · 2021: 8 · 2020: 1 · 2019: 1 · 2018: 4 · 2017: 1 · 2016: 3 · 2015: 5 · 2014: 4
- FWCI
- 2.60
- Type
- journal article
- Language
- en
- Open access
- green
- www.ncbi.nlm.nih.gov
- Locations
- Schizophrenia Research (publishedVersion)
- PubMed (publishedVersion)
- Europe PMC (PubMed Central) (acceptedVersion)
- PubMed Central (acceptedVersion)
- Carolina Digital Repository (University of North Carolina at Chapel Hill) (submittedVersion)
- UNC Libraries
- Funders
- National Institute of Mental Health (N01 MH900001)
- Foundation for the National Institutes of Health
- Topics
- Health Sciences › Medicine › Psychiatry and Mental health › Schizophrenia research and treatment
- Health Sciences › Medicine › Cardiology and Cardiovascular Medicine › Cardiac Health and Mental Health
- Health Sciences › Medicine › Psychiatry and Mental health › Bipolar Disorder and Treatment
- Keywords
- aripiprazole, olanzapine
- MeSH terms
- Aripiprazole, Quetiapine Fumarate, Olanzapine, Adult, Benzodiazepines, Coronary Artery Disease, Dibenzothiazepines, Female, Humans, Longitudinal Studies, Male, Middle Aged, Piperazines, Antipsychotic Agents, Multicenter Studies as Topic, Quinolones, Odds Ratio, Risperidone, Metabolic Syndrome, Drug Substitution
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