TY - JOUR
T1 - The association between weight change and symptom reduction in the CATIE schizophrenia trial
AU - Hermes, Eric
AU - Nasrallah, Henry
AU - Davis, Vicki
AU - Meyer, Jonathan
AU - McEvoy, Joseph Patrick
AU - Goff, Donald
AU - Davis, Sonia
AU - Stroup, T. Scott
AU - Swartz, Marvin
AU - Lieberman, Jeffrey
AU - Rosenheck, Robert
N1 - Funding Information:
Dr. Lieberman reports having received research funding from AstraZeneca Pharmaceuticals LP, Bristol-Myers Squibb, GlaxoSmithKline, Janssen Pharmaceutica Products, and Pfizer Inc.; and consulting and educational fees from AstraZeneca Pharmaceuticals LP, Bristol-Myers Squibb, Eli Lilly and Co., Forest Pharmaceutical Company, GlaxoSmithKline, Janssen Pharmaceutica Products, Novartis, Pfizer Inc., and Solvay.
Funding Information:
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.
Funding Information:
Dr. Stroup reports having received research funding from Eli Lilly and Co.; and consulting fees from Janssen Pharmaceutica Products, GlaxoSmithKline, and Bristol-Myers Squibb.
Funding Information:
Dr. McEvoy reports having received research funding from AstraZeneca, Forest Research Institute, Eli Lilly and Co., Janssen Pharmaeutica, and Pfizer Inc.; consulting or advisory board fees from Pfizer Inc. and Bristol-Myers Squibb; and lecture fees from Janssen Pharmaceutica, and Bristol-Myers Squibb.
Funding Information:
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.
Funding Information:
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.
Copyright:
Copyright 2011 Elsevier B.V., All rights reserved.
PY - 2011/5
Y1 - 2011/5
N2 - 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.
AB - 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.
KW - Antipsychotic agents
KW - Body mass index
KW - Lipids
KW - Schizophrenia
KW - Treatment outcome
KW - Weight gain
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U2 - 10.1016/j.schres.2011.01.022
DO - 10.1016/j.schres.2011.01.022
M3 - Article
C2 - 21334853
AN - SCOPUS:79955480406
SN - 0920-9964
VL - 128
SP - 166
EP - 170
JO - Schizophrenia Research
JF - Schizophrenia Research
IS - 1-3
ER -