# The effect of combining surgical or endoscopic bariatric interventions with anti-obesity medication or probiotics on weight loss: a narrative review

**Authors:** J. R. de Waal, M. Nieuwdorp, V. E. A. Gerdes

PMC · DOI: 10.3389/fendo.2026.1680182 · Frontiers in Endocrinology · 2026-02-04

## TL;DR

This review explores how combining bariatric procedures with anti-obesity medications or probiotics affects weight loss, finding that GLP-1 medications are most effective.

## Contribution

The paper provides a narrative review of combining bariatric interventions with anti-obesity medications or probiotics, highlighting the superior efficacy of GLP-1 receptor agonists.

## Key findings

- Combining GLP-1 receptor agonists with endoscopic sleeve gastroplasty leads to greater weight loss than ESG alone.
- Non-GLP-1 anti-obesity medications show less consistent and smaller weight loss effects.
- Probiotics and prebiotics combined with bariatric surgery do not significantly improve weight loss compared to placebo.

## Abstract

Obesity is a multifactorial chronic disease associated with multiple health complications. While bariatric surgery and endoscopic sleeve gastroplasty (ESG) are effective treatments for severe obesity, patients may still experience challenges such as weight regain or inadequate weight loss. As a result, combining these interventions with adjunctive treatment such as anti-obesity medication (AOM) or probiotics has become an area of increasing clinical interest. This narrative review summarizes the current evidence on the effect of combining surgical or endoscopic bariatric interventions with AOM or probiotics. Available studies suggest that the combination of GLP-1 receptor agonists (GLP-1 RA) and ESG leads to more weight loss than ESG alone. In contrast, non-GLP-1 RA medication show less consistent benefits and generally lower weight loss. GLP-1 RAs and tirzepatide show clinically relevant short term weight loss in patients with weight regain or insufficient weight loss after bariatric surgery. Other AOM, such as topiramate, phentermine, orlistat and bupropion/naltrexone result in more modest and variable outcomes. Relatively small studies on probiotics and prebiotics in combination with bariatric surgery do not find a statistically significant difference in weight loss between probiotic and placebo groups. Although small benefits in waist circumference, liver enzymes and vitamin uptake are mentioned, the effects are modest and not consistent across studies. In conclusion, combining AOM, especially GLP-1 RAs, with surgical or endoscopic obesity treatments appears to enhance weight loss in patients with suboptimal outcomes. These findings support the use of AOM as an adjunct to bariatric procedures. In addition, additional adequately powered studies are needed to evaluate the role for probiotics in improving weight loss after bariatric surgery. Future research should focus on long-term outcomes, side effects, and identifying patient subgroups that may benefit most from combined therapy.

## Linked entities

- **Chemicals:** GLP-1 (PubChem CID 16133831), tirzepatide (PubChem CID 163285897), topiramate (PubChem CID 5284627), phentermine (PubChem CID 4771), orlistat (PubChem CID 3034010), bupropion (PubChem CID 444), naltrexone (PubChem CID 5360515)
- **Diseases:** obesity (MONDO:0011122)

## Full-text entities

- **Genes:** GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, KITLG (KIT ligand) [NCBI Gene 4254] {aka DCUA, DFNA69, FPH2, FPHH, KL-1, Kitl}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], GCG (glucagon) [NCBI Gene 2641] {aka GLP-1, GLP1, GLP2, GRPP}, GLP1R (glucagon like peptide 1 receptor) [NCBI Gene 2740] {aka GLP-1, GLP-1-R, GLP-1R}
- **Diseases:** AOM (MESH:D009765), nausea (MESH:D009325), Weight Regain (MESH:D055191), diarrhea (MESH:D003967), osteoarthritis (MESH:D010003), metabolic dysfunction (MESH:D008659), steatotic liver disease (MESH:D008107), GIS (MESH:D012817), inflammation (MESH:D007249), gastroesophageal reflux (MESH:D005764), dyslipidemia (MESH:D050171), gallstone (MESH:D042882), diabetes (MESH:D003920), asthma (MESH:D001249), RYGB (MESH:D013272), obstructive sleep apnea (MESH:D020181), type 2 diabetes (MESH:D003924), constipation (MESH:D003248), SIBO (MESH:D001765), hypertension (MESH:D006973), Excess weight loss (MESH:D015431), insulin resistance (MESH:D007333)
- **Chemicals:** Phentermine (MESH:D010645), Metformin (MESH:D008687), iron (MESH:D007501), cholesterol (MESH:D002784), blood glucose (MESH:D001786), AOMs (MESH:D001397), triglycerides (MESH:D014280), bupropion (MESH:D016642), RA (MESH:D011883), UDCA (MESH:D014580), prebiotics (MESH:D056692), lipid (MESH:D008055), lorcaserin (MESH:C506658), vitamin B12 (MESH:D014805), Topiramate (MESH:D000077236), glucose (MESH:D005947), calcium (MESH:D002118), AOM (-), sibutramine (MESH:C058254), orlistat (MESH:D000077403), naltrexone (MESH:D009271), zonisamide (MESH:D000078305), fatty acid (MESH:D005227)
- **Species:** Bifidobacterium animalis subsp. lactis (subspecies) [taxon 302911], gut metagenome (species) [taxon 749906], Akkermansia muciniphila (species) [taxon 239935], Lactobacillus acidophilus NCFM (strain) [taxon 272621], Homo sapiens (human, species) [taxon 9606]

## Full text

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## References

51 references — full list in the complete paper: https://tomesphere.com/paper/PMC12913063/full.md

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Source: https://tomesphere.com/paper/PMC12913063