Zonisamide in the treatment of binge eating disorder with obesity: A randomized controlled trial

被引:99
|
作者
McElroy, Susan L.
Kotwal, Renu
Guerdjikova, Anna I.
Welge, Jeffrey A.
Nelson, Erik B.
Lake, Kathleen A.
D'Alessio, David A.
Keck, Paul E., Jr.
Hudson, James I.
机构
[1] Univ Cincinnati, Coll Med, Psychopharmacol Res Program, Dept Psychiat, Cincinnati, OH 45267 USA
[2] Univ Cincinnati, Coll Med, Div Endocrinol, Dept Internal Med, Cincinnati, OH 45267 USA
[3] Cincinnati Vet Affairs Med Ctr, Gen Clin Res Ctr, Cincinnati, OH USA
[4] Cincinnati Vet Affairs Med Ctr, Mental Hlth Serv Line, Cincinnati, OH USA
[5] Harvard Univ, Sch Med, Dept Psychiat, Belmont, MA 02178 USA
[6] Harvard Univ, McLean Hosp, Belmont, MA 02178 USA
关键词
D O I
10.4088/JCP.v67n1209
中图分类号
B849 [应用心理学];
学科分类号
040203 ;
摘要
Objective: Binge eating disorder (BED) is associated with obesity. Zonisamide is a novel antiepileptic drug associated with weight loss. The purpose of this study was to evaluate zonisamide in the treatment of BED associated with obesity. Method: In this 16-week, single-center, randomized, double-blind, placebo-controlled, flexible-dose (100-600 mg/day) trial, 60 outpatients with DSM-IV-TR BED received zonisamide (N = 30) or placebo (N = 30). The primary outcome measure was weekly frequency of binge eating episodes. 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 5, 2003, through October 1, 2004. Results: Compared with placebo, zonisamide was associated with a significantly greater rate of reduction in binge eating episode frequency (p = .021), body weight (p < .001), BMI (p = .001), and scores on the Clinical Global Impressions-Severity scale (p < .001), Yale-Brown Obsessive Compulsive Scale Modified for Binge Eating (p < .001), and Three Factor Eating Questionnaire disinhibition scales (p < .001). Plasma ghrelin concentrations increased with zonisamide but decreased with placebo (p = .001). The mean (SD) zonisamide daily dose at endpoint evaluation was 436 (159) mg/day. Twelve patients (N = 8 receiving zonisamide, N = 4 receiving placebo) discontinued because of adverse events. The most common reasons for discontinuing zonisamide were accidental injury with bone fracture (N = 2), psychological complaints (N = 2), and cognitive complaints (N = 2). Conclusion: Zonisamide was efficacious, but not well tolerated, in the short-term treatment of BED associated with obesity.
引用
收藏
页码:1897 / 1906
页数:12
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