Efficacy of Naltrexone/Bupropion in Treatment of Binge Eating: A Systematic Review and Meta-Analysis

Author:

Moawad Mostafa Hossam-Eldin12,Sadeq Mohammed Ahmed3ORCID,Abbas Abdallah4,Ghorab Reem Mohamed Farouk3,Serag Ibrahim5ORCID,Hendawy Mohamed6,Alkasaby Muhammad7ORCID

Affiliation:

1. Clinical Department, Faculty of Pharmacy, Alexandria University, Alexandria 21521, Egypt

2. Faculty of Medicine, Suez Canal University, Ismailia 41522, Egypt

3. Emergency Medicine Department, Elsheikh Zayed Specialized Hospital, Elsheikh Zayed City 12588, Egypt

4. Faculty of Medicine, Al-Azhar University, Damietta 34517, Egypt

5. Faculty of Medicine, Mansoura University, Mansoura 35516, Egypt

6. Faculty of Pharmacy, Alexandria University, Alexandria 21521, Egypt

7. Centre for Global Mental Health, London School of Hygiene & Tropical Medicine, London WC1E 7HT, UK

Abstract

Background: As the most widespread eating disorder in the world now, binge eating disorder (BED) is a mental condition characterized by recurrent periods of excessive food consumption and an inability to regulate one’s portion sizes. The utilization of a bupropion–naltrexone (NB) combination has been suggested as a potential therapeutic approach for BED. Assessing the effectiveness of NB in the treatment of BED and its accompanying obesity is the purpose of this research. Methods: A comprehensive search was conducted in order to obtain any pertinent articles. PubMed, Scopus, Web of Science, and Cochrane Clinical Trials were consulted against in the databases that were searched. In our final meta-analysis, we incorporated interventional or observational studies that documented the effects of NB therapy for binge eating in adults. We also examined the difference in the mean change between the NB and placebo groups, as well as the disparity in outcomes before and after treatment. Results: This study shows that the use of an NB combination is associated with a statistically significant reduction in the weight, BMI, and Binge Eating Scale (BES) of the patients compared to their weight before treatment with MD: −8.52 (95% CI: −10.01–−6.94, p < 0.00001), MD: −4.95 (95%CI: −9.72–−0.17, p = 0.04), and MD: −7.66 (95%CI: −14.36–0.96, p = 0.02), respectively. The absolute mean change was statistically significantly higher in the drug combination group compared to the placebo group. Conclusions: NB showed efficacy in the improvement of the weight and psychiatric symptoms associated with BED and this provides a promising treatment option.

Publisher

MDPI AG

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