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The association between weight change and symptom reduction in the CATIE schizophrenia trial

  • Eric Hermes(corresponding author)
    ,
  • Henry Nasrallah
    ,
  • Vicki Davis
    ,
  • Jonathan Meyer
    ,
  • ,
  • Donald Goff
*Corresponding author for this work
  • Yale University
    ,
  • University of Cincinnati
    ,
  • NeuroCog Trials, Inc.
    ,
  • University of California at San Diego
    ,
  • ,
  • Harvard 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

Background: Weight gain and changes in metabolic indicators associated with some antipsychotics may be related to symptom improvement and thus an unavoidable correlate of clinical benefit. Methods: Data from the CATIE schizophrenia trial comparing the effectiveness of perphenazine, olanzapine, risperidone, quetiapine and ziprasidone in a randomized, double-blind, trial over 18. months were used to evaluate the relationship between percent change in body mass index (BMI) and change in total serum cholesterol and triglycerides with the Positive and Negative Syndrome Scale (PANSS) score. Analysis of covariance for observations at 3. months and a mixed effects model for all observations up to 18. months adjusted for potentially confounding variables were used to examine these associations. Results: In both models, there was a significant association (p=0.001) between change in PANSS total score and percent change in BMI, equating to a 0.28 and 0.21 point decrease in PANSS total score (range 30-210) per 1% increase in BMI respectively. Change in BMI accounted for 3% or less of variance for change in PANSS scores. There was no evidence that the association of symptoms and weight gain differed across medications in spite of substantial differences in weight gain and other metabolic measures. Neither total serum cholesterol nor triglyceride levels displayed a significant association with change in PANSS. Conclusion: The magnitude of the relationship between change in BMI and PANSS was too small to be clinically important, indicating that switching medications to one with less metabolic risk is unlikely to result in meaningful loss of clinical benefit.

Publication Information

Output type

Scholary Output:
Contribution to journal
Article
Peer-review

Original language

English (US)

Pages from-to (Number of pages)

Pages 166-170 (5 pages)

Journal (Volume, Issue Number)

Schizophrenia Research (Volume 128, Issue 1-3)

Publication milestones

  • Published - 05/2011

Publication status

Published - 05/2011

ISSN

0920-9964

Publication IDs

  • Scopus: 79955480406
  • PubMed: 21334853

Publication metrics

Metrics

Scopus
citations
SciVal
citations
54
Fractional count
1
Fractional count
0.09
Fractional count
10
Fractional count
0.91
Fractional count
1
Fractional count
1
SciVal
FWCI
1.62
SciVal
Author count
11
SciVal
Paper percentile
92
SciVal
Top percentile
10

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Captures
84
Social media
26
Citation count
76

Funding Details

Dr. Swartz reports having received research funding from Eli Lilly and Co., and consulting and educational fees from AstraZeneca Pharmaceuticals LP, Bristol-Myers Squibb, Eli Lilly and Co., and Pfizer Inc. Dr. Stroup reports having received research funding from Eli Lilly and Co.; and consulting fees from Janssen Pharmaceutica Products, GlaxoSmithKline, and Bristol-Myers Squibb. This analysis was supported by the New England Mental Illness Research and Education Center. The funding source had no role in the design, analysis or interpretation of data or in the preparation of the report or decision to publish. Dr. Meyer reports having received research support from Bristol-Myers Squibb and Pfizer, Inc., and has received speaking or advising fees from Bristol-Myers Squibb, Janssen Pharmaceutica, Pfizer, Inc., and Wyeth.
FundersFunding number
Eli Lilly and Co.
-
New England Mental Illness Research and Education Center
-
NIMH
K24MH002025
BMS
-
Pfizer
-
AstraZeneca
-
GSK
-