Cited by 39Schizophrenia research and treatmentCardiac Health and Mental HealthBipolar Disorder and Treatment

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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Stroup, T. Scott, Byerly, Matthew J., Nasrallah, Henry A., Ray, Neepa, Khan, Ahsan Y., Lamberti, J. Steven, Glick, Ira D., Steinbook, Richard M. +2 more·2013·Schizophrenia Research

Abstract

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.”

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Research works printed but not linked: 21

  1. Third Report of the National Cholesterol Education Program (NCEP) Expert Panel on Detection, Evaluation, and Treatment of High Blood Cholesterol in Adults (Adult Treatment Panel III) final report Circulation 106 25 3143 3421 12485966
  2. Consensus development conference on antipsychotic drugs and obesity and diabetes J Clin Psychiatry 65 2 267 272 15003083
  3. Alberti KG Zimmet P 2005 The metabolic syndrome--a new worldwide definition Lancet 366 9491 1059 1062 16182882
  4. Allison DB Mentore JL 1999 Antipsychotic-induced weight gain: a comprehensive research synthesis The American journal of psychiatry 156 11 1686 1696 10553730
  5. Brar JS Ganguli R 2005 Effects of behavioral therapy on weight loss in overweight and obese patients with schizophrenia or schizoaffective disorder J Clin Psychiatry 66 2 205 212 15705006
  6. Bushe CJ Taylor M 2010 Mortality in schizophrenia: a measurable clinical endpoint Journal of psychopharmacology 24 4 Suppl 17 25 20923917 PMC2951589
  7. Citrome L 2011 Iloperidone, asenapine, and lurasidone: a brief overview of 3 new second-generation antipsychotics Postgraduate medicine 123 2 153 162 21474903
  8. El-Sayeh HG Morganti C 2006 Aripiprazole for schizophrenia Cochrane database of systematic reviews 2 CD004578 PMC11361475 16625607
  9. Ganguli R 2007 Behavioral therapy for weight loss in patients with schizophrenia J Clin Psychiatry 68 Suppl 4 19 25 17539696
  10. Goff DC Sullivan LM 2005 A comparison of ten-year cardiac risk estimates in schizophrenia patients from the CATIE study and matched controls Schizophrenia research 80 1 45 53 16198088
  11. Hennekens CH Hennekens AR 2005 Schizophrenia and increased risks of cardiovascular disease American heart journal 150 6 1115 1121 16338246
  12. Holt RI Pendlebury J 2010 Intentional weight loss in overweight and obese patients with severe mental illness: 8-year experience of a behavioral treatment program The Journal of clinical psychiatry 71 6 800 805 20361917
  13. Kim SH Ivanova O 2007 Metabolic impact of switching antipsychotic therapy to aripiprazole after weight gain: a pilot study Journal of clinical psychopharmacology 27 4 365 368 17632220
  14. Leucht S Komossa K 2009 A meta-analysis of head-to-head comparisons of second-generation antipsychotics in the treatment of schizophrenia Am J Psychiatry 166 2 152 163 19015230
  15. McEvoy JP Meyer JM 2005 Prevalence of the metabolic syndrome in patients with schizophrenia: baseline results from the Clinical Antipsychotic Trials of Intervention Effectiveness (CATIE) schizophrenia trial and comparison with national estimates from NHANES III Schizophr Res 80 1 19 32 16137860
  16. Nasrallah HA Meyer JM 2006 Low rates of treatment for hypertension, dyslipidemia and diabetes in schizophrenia: data from the CATIE schizophrenia trial sample at baseline Schizophr Res 86 1–3 15 22 16884895
  17. Newcomer JW 2005 Second-generation (atypical) antipsychotics and metabolic effects: a comprehensive literature review CNS Drugs 19 Suppl 1 1 93 15998156
  18. Reaven GM 2005 The metabolic syndrome: requiescat in pace Clinical chemistry 51 6 931 938 15746300
  19. Stroup TS McEvoy JP 2011 A Randomized Trial Examining the Effectiveness of Switching From Olanzapine, Quetiapine, or Risperidone to Aripiprazole to Reduce Metabolic Risk: Comparison of Antipsychotics for Metabolic Problems (CAMP) The American journal of psychiatry 168 9 947 956 21768610 PMC3773729
  20. Taylor F Ward K 2011 Statins for the primary prevention of cardiovascular disease Cochrane database of systematic reviews 1 CD004816 PMC4164175 21249663
  21. Wilson PW D’Agostino RB 1998 Prediction of coronary heart disease using risk factor categories Circulation 97 18 1837 1847 9603539

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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)
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
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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