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Journal of Child and Adolescent Psychopharmacology
Divalproex Sodium Reduces Overall Aggression in Youth at High Risk for Bipolar Disorder

To cite this article:
Kirti Saxena, Meghan Howe, Diana Simeonova, Hans Steiner, Kiki Chang. Journal of Child and Adolescent Psychopharmacology. 2006, 16(3): 252-259. doi:10.1089/cap.2006.16.252.

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Kirti Saxena, M.D.
Stanford University, School of Medicine, Department of Psychiatry and Behavioral Sciences, Division of Child Psychiatry and Child Development, Stanford, California.
Meghan Howe, M.S.W.
Stanford University, School of Medicine, Department of Psychiatry and Behavioral Sciences, Division of Child Psychiatry and Child Development, Stanford, California.
Diana Simeonova, B.S.
Stanford University, School of Medicine, Department of Psychiatry and Behavioral Sciences, Division of Child Psychiatry and Child Development, Stanford, California.
Hans Steiner, M.D.
Stanford University, School of Medicine, Department of Psychiatry and Behavioral Sciences, Division of Child Psychiatry and Child Development, Stanford, California.
Kiki Chang, M.D.
Stanford University, School of Medicine, Department of Psychiatry and Behavioral Sciences, Division of Child Psychiatry and Child Development, Stanford, California.

Introduction: The psychopharmacology of aggression in youth is relatively unexplored, even though such maladaptive aggression manifests across many different diagnoses.

Methods: This study was a 12-week, open-label trial with divalproex sodium (DVPX) in 24 bipolar offspring 6–18 years of age (mean age = 11.3 years; 17 boys) with mixed diagnoses of major depression, cyclothymia, attention-deficit/hyperactivity disorder (ADHD), and oppositional defiant disorder (ODD). The Overt Aggression Scale (OAS) was used to measure aggression in 4-week intervals. We measured serum gamma-butyric acid (GABA) and glutamate levels at baseline and week 12.

Results: Seventy-one percent of evaluable subjects were considered responders to DVPX treatment by the OAS. There was a significant correlation between the Young Mania Rating Scale (YMRS) and OAS scores at week 0 (p = 0.036) and week 12 (p = 0.025). Serum DVPX level did not correlate with treatment response.

Conclusions: These youths who are at high risk for bipolar disorder experienced an overall decrease in aggressive behavior in response to DVPX. Age or gender did not predict a positive response to DVPX. This study is the first report of treatment efficacy of a mood stabilizer for aggression in youth at high risk for bipolar disorder.

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