# Efficacy and Safety of Lisdexamfetamine Versus Topiramate Versus Naltrexone/Bupropion in Individuals With Binge Eating Disorder: A Network Meta‐Analysis

**Authors:** Tamer Hodrob, Ibrahim Ismail, Alaaeddin Abusalameh, Celina R. Andonie, Omar Ayesh, Hazem Ayesh

PMC · DOI: 10.1002/erv.70035 · European Eating Disorders Review · 2025-09-22

## TL;DR

The study compares three medications for binge eating disorder and finds lisdexamfetamine and topiramate most effective in reducing binge episodes and promoting weight loss.

## Contribution

A network meta-analysis comparing lisdexamfetamine, topiramate, and naltrexone/bupropion for BED efficacy and safety.

## Key findings

- Lisdexamfetamine and topiramate significantly reduced binge eating frequency compared to placebo.
- Topiramate caused the most weight loss, while naltrexone/bupropion showed modest weight effects but no significant binge reduction.
- Lisdexamfetamine was linked to higher dry mouth and gastrointestinal side effects, but no significant increase in serious adverse events.

## Abstract

To compare the efficacy and safety of lisdexamfetamine, topiramate, and naltrexone/bupropion for treating binge eating disorder (BED) using network meta‐analysis.

We systematically searched PubMed, Scopus, ClinicalTrials.gov, and Cochrane Central up to February 2025 for randomized controlled trials evaluating these medications versus placebo in adults with BED. Primary outcomes were changes in binge eating frequency and body weight; secondary outcomes included serious adverse events, discontinuation rates, and common side effects. A frequentist random‐effects network meta‐analysis was performed.

Twelve trials (n = 1988) met inclusion criteria. Both lisdexamfetamine (MD −1.61, 95% CI: −2.41 to −0.81) and topiramate (MD −1.63, 95% CI: −2.53 to −0.74) significantly reduced binge eating frequency versus placebo, with comparable efficacy. Topiramate produced the greatest weight loss (MD −5.5 kg), followed by lisdexamfetamine (−4.6 kg). Naltrexone/bupropion did not significantly reduce binge frequency (MD −2.07, 95% CI: −4.45 to 0.31). Lisdexamfetamine was associated with higher risks of dry mouth and gastrointestinal events. No significant increase in serious adverse events was observed for any medication.

Topiramate and lisdexamfetamine are effective for reducing binge episodes and weight in BED. Naltrexone/bupropion showed modest weight effects but lacked clear efficacy for binge reduction. These findings support topiramate and lisdexamfetamine as primary pharmacologic options for BED.

Both lisdexamfetamine and topiramate significantly reduce binge eating frequency and promote weight loss in adults with binge eating disorder.Naltrexone/bupropion does not show significant efficacy for reducing binge eating episodes, though it is associated with modest weight loss.Lisdexamfetamine is associated with increased dry mouth and gastrointestinal side effects; serious adverse events were not significantly increased for any treatment.

Both lisdexamfetamine and topiramate significantly reduce binge eating frequency and promote weight loss in adults with binge eating disorder.

Naltrexone/bupropion does not show significant efficacy for reducing binge eating episodes, though it is associated with modest weight loss.

Lisdexamfetamine is associated with increased dry mouth and gastrointestinal side effects; serious adverse events were not significantly increased for any treatment.

## Linked entities

- **Chemicals:** lisdexamfetamine (PubChem CID 11597698), topiramate (PubChem CID 5284627), naltrexone (PubChem CID 5360515), bupropion (PubChem CID 444)
- **Diseases:** binge eating disorder (MONDO:0005582)

## Full-text entities

- **Diseases:** weight loss (MESH:D015431), BED (MESH:D056912), dry mouth (MESH:D014987), binge eating (MESH:D002032)
- **Chemicals:** Bupropion (MESH:D016642), Lisdexamfetamine (MESH:D000069478), Topiramate (MESH:D000077236), Naltrexone (MESH:D009271)

## Full text

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## Figures

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## References

49 references — full list in the complete paper: https://tomesphere.com/paper/PMC12862547/full.md

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Source: https://tomesphere.com/paper/PMC12862547