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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)

  • T. Scott Stroup(corresponding author)
    ,
  • ,
  • Kimberly D. Ring
    ,
  • Robert H. Hamer
    ,
  • Lisa M. LaVange
    ,
  • Marvin S. Swartz
*Corresponding author for this work
  • Duke University
    ,
  • Columbia University
    ,
  • University of Colorado Denver
    ,
  • University of North Carolina at Chapel Hill
    ,
  • Yale University
    ,
Scholary Output:
Contribution to journal
Article
Peer-review

Open access

Sustainable Development Goals

  • SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well

Abstract

Objective: The authors conducted a multisite randomized controlled trial examining the strategy of switching from olanzapine, quetiapine, or risperidone to aripiprazole to ameliorate metabolic risk factors for cardiovascular disease. Method : Patients with schizophrenia or schizoaffective disorder with a body mass index ≥27 and non-high-density lipoprotein (non-HDL) cholesterol ≥130 mg/dl who were on a stable treatment dosage of olanzapine, quetiapine, or risperidone were randomly assigned to switch to aripiprazole (N=109) for 24 weeks or stay on their current medication (N=106). All participants were enrolled in a behaviorally oriented diet and exercise program. Clinical raters were blinded to treatment assignment. The primary and key secondary outcomes were change in non-HDL cholesterol and efficacy failure, respectively. Results : The prespecified primary analysis included 89 switchers and 98 stayers who had at least one postbaseline non-HDL cholesterol measurement. The least squares mean estimates of non-HDL cholesterol decreased more for the switch group than for the stay group (-20.2 mg/ dl and -10.8 mg/dl, respectively). Switching was associated with larger weight reductions (least squares mean=2.9 kg) and a net reduction of serum triglycerides of 32.7 mg/dl. Twenty-two switchers (20.6%) and 18 stayers (17.0%) experienced protocol- defined efficacy failure. Forty-seven switchers (43.9%) and 26 stayers (24.5%) discontinued the assigned antipsychotic medication before 24 weeks. Conclusion : Switching to aripiprazole led to improvement of non-HDL cholesterol levels and other metabolic parameters. Rates of efficacy failure were similar between groups, but switching to aripiprazole was associated with a higher rate of treatment discontinuation. In the context of close clinical monitoring, switching from an antipsychotic with high metabolic risk to one with lower risk to improve metabolic parameters is an effective strategy.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 947-956 (10 pages)

Journal (Volume, Issue Number)

American Journal of Psychiatry (Volume 168, Issue 9)

Publication milestones

  • Published - 09/2011

Publication status

Published - 09/2011

ISSN

0002-953X

Publication IDs

  • Scopus: 80052490081
  • PubMed: 21768610

Publication metrics

Metrics

Scopus
citations
SciVal
FWCI
6.37
SciVal
Author count
10
SciVal
citations
126
SciVal
Paper percentile
98
SciVal
Top percentile
5
Fractional count
1
Fractional count
0.10
Fractional count
9
Fractional count
0.90
Fractional count
1
Fractional count
1

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Social media
14
Citation count
177
Captures
228

Funding Details

FunderFunding number
NIMH
Z01MH900001