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Efficacy of rimonabant in obese patients with binge eating disorder
Z Pataky1, C Gasteyger, O Ziegler
1Department of Community Medicine, Service of Therapeutic Education for Chronic Diseases, World Health Organization Collaborating Centre, University Hospitals of Geneva, Geneva, Switzerland. zoltan.pataky@hcuge.ch
Abstract:
In obesity, a dysregulation of the endocannabinoid system has been shown. The endocannabinoid receptor blockage by rimonabant demonstrated interesting metabolic effects. However, the role of rimonabant in weight loss of patients with binge eating disorder has not been investigated. Thus, our aim was to evaluate the effects of rimonabant on body weight in obese patients with binge eating disorders. This multicenter, randomized, double-blind, placebo-controlled study included 289 obese subjects (age 18-70 years, body mass index 30-45 kg/m(2)) with binge eating disorders. Subjects were randomized (1:1) to receive rimonabant 20 mg/day or placebo for 6 months. In total, 289 participants (age: 43.2±10.5 yrs, 91% of women) were randomized. The completer rate was similar (71%) in both treatment and placebo groups. Participants treated with rimonabant lost 4.7±5.2% of their initial body weight, vs. 0.4±4.5% in the placebo group (difference between both groups: 4.4±0.6 kg, p<0.0001). The rimonabant group showed a greater reduction on the binge eating scale total score (mean±SD - 40.9±35.2%) vs. placebo ( - 29.9±34.6%, p=0.02). The incidence of treatment emergent adverse events was comparable in both the rimonabant (82.5%) and placebo (76.0%) group. Discontinuations due to treatment emergent adverse events occurred in 13.3% rimonabant-treated vs. 6.2% placebo-treated participants. In conclusion, this is the only randomised, placebo-controlled, double-blind trial having assessed the effect of rimonabant in patients with binge eating disorders. The rimonabant treatment reduced body weight significantly more than placebo in obese subjects with binge eating. Trial registration number (clinicaltrials.gov): NCT00481975.
Insights
Rimonabant significantly reduced body weight and binge eating behaviors in obese patients with binge eating disorders compared to placebo. This study provides evidence for rimonabant
Area of Science:
- Endocrinology and Metabolism
- Psychiatry and Behavioral Science
- Pharmacology
Background:
- Obesity is associated with endocannabinoid system dysregulation.
- Endocannabinoid receptor blockade with rimonabant shows metabolic effects.
- The efficacy of rimonabant for weight loss in binge eating disorder (BED) is unexplored.
Purpose of the Study:
- To evaluate the effects of rimonabant on body weight in obese patients diagnosed with BED.
- To assess rimonabant's impact on binge eating episodes and severity.
Main Methods:
- A multicenter, randomized, double-blind, placebo-controlled trial.
- 289 obese subjects (BMI 30-45 kg/m²) with BED were randomized (1:1) to receive rimonabant 20 mg/day or placebo for 6 months.
- Primary outcome: change in body weight. Secondary outcome: change in Binge Eating Scale (BES) score.
Main Results:
- Rimonabant treatment resulted in a significant mean weight loss of 4.7±5.2% versus 0.4±4.5% in the placebo group (p<0.0001).
- The rimonabant group demonstrated a greater reduction in BES total score (–40.9±35.2%) compared to placebo (–29.9±34.6%, p=0.02).
- Adverse event incidence was comparable, but discontinuations due to adverse events were higher in the rimonabant group (13.3% vs. 6.2%).
Conclusions:
- Rimonabant significantly reduced body weight and binge eating severity in obese patients with BED.
- This trial is the first randomized, placebo-controlled study to demonstrate rimonabant's efficacy in this population.
- Further research is warranted to balance efficacy with safety concerns regarding adverse events.
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