Atomoxetine in the Treatment of Binge-Eating Disorder: A Randomized Placebo-Controlled Trial

Susan L. McElroy, MD; Anna Guerdjikova, PhD; Renu Kotwal, MD; Jeffrey A. Welge, PhD; Erik B. Nelson, MD; Kathleen A. Lake, MSW; Paul E. Keck, Jr., MD; and James I. Hudson, MD, ScD

Published: March 15, 2007

Article Abstract

Objective: Binge-eating disorder (BED) is associated with obesity. Atomoxetine is a highly selective norepinephrine reuptake inhibitor associated with weight loss. The purpose of this study was to evaluate atomoxetine in the treatment of BED.

Method: In this 10-week, single-center, randomized, double-blind, placebo-controlled, flexible dose (40-120 mg/day) trial, outpatients with DSM-IV-TR BED received atomoxetine or placebo. The primary outcome measure was binge-eating episode frequency. The primary analysis of efficacy was a longitudinal analysis of the intent-to-treat sample, with treatment-by-time interaction as the effect measure. Patients were enrolled from September 2004 through October 2005.

Results: Compared with placebo (N = 20), atomoxetine (N = 20) was associated with a significantly greater rate of reduction in binge-eating episode frequency, as well as in binge day frequency, weight, body mass index, and scores on the Clinical Global Impressions-Severity of Illness scale, Yale-Brown Obsessive Compulsive Scale Modified for Binge Eating obsession subscale, and Three Factor Eating Questionnaire hunger subscale. The mean (SD) atomoxetine daily dose at endpoint evaluation was 106 (21) mg/day. Four patients (N = 3 receiving atomoxetine, N = 1 receiving placebo) discontinued because of adverse events. The reasons for atomoxetine discontinuation were increased depressive symptoms (N = 1), constipation (N = 1), and nervousness (N = 1).

Conclusion: Atomoxetine was efficacious and fairly well tolerated in the short-term treatment of BED.

Clinical Trials Registration: identifier NCT00327834′ ‹

Volume: 68

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