Volume 46, Issue 6 , Pages 687-700, June 2007
Weight Gain and Metabolic Effects of Mood Stabilizers and Antipsychotics in Pediatric Bipolar Disorder: A Systematic Review and Pooled Analysis of Short-Term Trials
ABSTRACT
Objective
To review weight and metabolic effects of mood-stabilizing treatments in pediatric bipolar disorder.
Method
Systematic PubMed/Medline search of studies reporting on change in weight and/or glucose/lipid values with mood-stabilizing drugs in at least nine pediatric patients with bipolar disorder.
Results
Nineteen studies, including 24 medication trials in 684 patients (mean age, 12.3 ± 2.9 years) were included. Youngsters received lithium, antiepileptics, or their combinations (n = 459), or second-generation antipsychotics, alone or combined with lithium or divalproex (n = 225), for 4 to 48 (mean, 15.4 ± 12.7) weeks. Weight increase was significant/clinically relevant in 18 (75.0%) trials. Weight loss was significant with topiramate (2 studies, 38 subjects) and present with aripiprazole (1 study, 14 subjects). In trials lasting ≤12 weeks, weight gain was greater with second-generation antipsychotics plus mood stabilizers (5.5 ± 1.8 kg) compared to mood-stabilizer monotherapy (1.2 ± 1.9 kg, p <.05, Cohen's d = 2.33) or mood-stabilizer cotreatment (2.1 ± 1.3 kg, p <.05, Cohen's d = 2.17), but not compared to antipsychotic monotherapy (3.4 ± 1.3 kg, p >.05, Cohen's d = 1.34). Nonfasting glucose/lipid changes were nonsignificant in two second-generation antipsychotic trials (n = 61, 8.9%).
Conclusions
Data are sparse regarding body composition effects and lacking for fasting metabolic effects of mood stabilizers in pediatric bipolar disorder. Combining antipsychotics with mood stabilizers seems to lead to greater weight gain than treatment with one or two mood stabilizers.
Key Words: bipolar disorder , second-generation antipsychotics , mood stabilizers , weight gain , metabolic abnormalities
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Supported by The Zucker Hillside Hospital NIMH Advanced Center for Intervention and Services Research for the Study of Schizophrenia MH 074543-01, and the NSLIJ Research Institute NIH General Clinical Research Center MO1RR018535. The author thanks Mani M. Pavuluri, M.D., for sharing unpublished results and Hanna M. Kester for her assistance with the manuscript.Disclosure: Dr. Correll serves as a consultant, advisor, and/or lecturer for AstraZeneca, Bristol-Myers Squibb, Otsuka, Eli Lilly, Intra-Cellular Therapeutics, Janssen, and Solvay.
PII: S0890-8567(09)62148-1
doi:10.1097/chi.0b013e318040b25f
© 2007 The American Academy of Child and Adolescent Psychiatry. Published by Elsevier Inc. All rights reserved.
Volume 46, Issue 6 , Pages 687-700, June 2007
