# Endobariatric Management of Metabolic Dysfunction-Associated Steatotic Liver Disease: A Narrative Review

**Authors:** Muaaz Masood, Reem Z. Sharaiha, Asma Siddique, Shanley Deal, Richard A. Kozarek

PMC · DOI: 10.3390/biomedicines14020345 · Biomedicines · 2026-02-02

## TL;DR

This paper reviews endoscopic bariatric treatments as a promising alternative to surgery for managing obesity and liver disease linked to metabolic dysfunction.

## Contribution

The paper provides a comprehensive review of primary and secondary endoscopic bariatric therapies for MASLD, focusing on their mechanisms, efficacy, and safety.

## Key findings

- Endoscopic bariatric therapies offer a less invasive alternative to surgery for treating MASLD and obesity.
- Primary EBMTs like intragastric balloons and sleeve gastroplasty show efficacy in weight loss and liver disease improvement.
- Secondary EBMTs, including outlet reduction and revisional procedures, are emerging as additional treatment options.

## Abstract

As the rates of type 2 diabetes and obesity have increased globally, the prevalence of metabolic dysfunction-associated steatotic liver disease (MASLD), previously termed non-alcoholic steatotic fatty liver disease (NAFLD), has risen concomitantly worldwide. MASLD is now the most common etiology of chronic liver disease and is the leading indication for liver transplantation in the United States. Patients with MASLD have an increased risk of progression to metabolic dysfunction-associated steatohepatitis (MASH), cirrhosis, hepatocellular carcinoma, extrahepatic malignancies, as well as liver- and cardiovascular-related mortality. Diet and lifestyle modifications with a goal of ≥10% total body weight loss—required to reverse steatosis, steatohepatitis, and fibrosis—are often challenging and ineffective. Although novel pharmacotherapies have recently been approved and others are in development, cost, adherence, and adverse effects remain potential limitations. Bariatric surgery, including Roux-en-Y gastric bypass and sleeve gastrectomy, is highly efficacious and a cost-effective treatment for obesity and associated medical problems. However, bariatric surgery may be associated with morbidity and mortality. Endoscopic bariatric and metabolic therapy (EBMT) has recently emerged as a promising treatment modality and offers an alternative to surgery. Primary EBMTs include intragastric balloon placement, aspiration therapy, endoscopic sleeve gastroplasty, duodenal mucosal resurfacing, duodenal–jejunal bypass liner, and primary obesity surgery endoluminal (POSE 2.0). Secondary EBMTs include transoral outlet reduction, argon plasma coagulation of the anastomosis, and revisional endoscopic sleeve procedure. We review the recent literature on primary EBMTs and secondary EBMTs for the treatment of obesity and MASLD, the pathophysiologic mechanisms, efficacy, safety, and patient outcomes in MASLD in this narrative review.

## Linked entities

- **Diseases:** type 2 diabetes (MONDO:0005148), obesity (MONDO:0011122), metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), metabolic dysfunction-associated steatohepatitis (MONDO:0007027), cirrhosis (MONDO:0005155), hepatocellular carcinoma (MONDO:0007256)

## Full-text entities

- **Genes:** CD79B (CD79b molecule) [NCBI Gene 974] {aka AGM6, B29, IGB, Igbeta}, APC (APC regulator of Wnt signaling pathway) [NCBI Gene 324] {aka BTPS2, DESMD, DP2, DP2.5, DP3, GS}, THRB (thyroid hormone receptor beta) [NCBI Gene 7068] {aka C-ERBA-2, C-ERBA-BETA, ERBA2, GRTH, NR1A2, PRTH}, 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}, GGTLC5P (gamma-glutamyltransferase light chain 5 pseudogene) [NCBI Gene 653590] {aka GGT}, PYY (peptide YY) [NCBI Gene 5697] {aka PYY-I, PYY1}, SLC17A5 (solute carrier family 17 member 5) [NCBI Gene 26503] {aka AST, ISSD, NSD, SD, SIALIN, SIASD}, LEP (leptin) [NCBI Gene 3952] {aka LEPD, OB, OBS}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695], GPT (glutamic--pyruvic transaminase) [NCBI Gene 2875] {aka AAT1, ALT, ALT1, GPT1, SGPT}, FASTK (Fas activated serine/threonine kinase) [NCBI Gene 10922] {aka FAST}
- **Diseases:** infection (MESH:D007239), coagulopathy (MESH:D001778), NAFLD (MESH:D065626), Crohn's disease (MESH:D003424), peptic ulcer disease (MESH:D010437), extrahepatic malignancies (MESH:D009369), Gastrointestinal perforation (MESH:D005767), Liver Fibrosis (MESH:D008103), abdominal pain (MESH:D015746), Weight loss (MESH:D015431), leak (MESH:D019559), DJBL (MESH:D007579), Insulin Resistance (MESH:D007333), chronic pancreatitis (MESH:D050500), OSA (MESH:C535586), ulcers (MESH:D014456), MASLD (MESH:D008107), hepatic abscess (MESH:D008100), portal hypertension (MESH:D006975), inflammation (MESH:D007249), injury to (MESH:D014947), gastric ulcers (MESH:D013276), GERD (MESH:D005764), esophagogastric varices (MESH:D014648), metabolic syndrome (MESH:D024821), hyperglycemia (MESH:D006943), hyperlipidemia (MESH:D006949), F2-3 fibrosis (MESH:D005355), dyslipidemia (MESH:D050171), hypertension (MESH:D006973), pain (MESH:D010146), Metabolic Dysfunction (MESH:D008659), hepatocellular carcinoma (MESH:D006528), dumping syndrome (MESH:D004377), strictures (MESH:D003251), DMR (MESH:D004382), hiatal hernia (MESH:D006551), gastrointestinal bleeding (MESH:D006471), celiac disease (MESH:D002446), nausea, vomiting (MESH:D020250), fatty liver (MESH:D005234), type 2 diabetes (MESH:D003924), obstructive sleep apnea (MESH:D020181), Obesity (MESH:D009765), polyps (MESH:D011127), weight regain (MESH:D055191), nausea (MESH:D009325), perforations (MESH:D057112), intestinal obstructions (MESH:D007415), neoplastic lesions (MESH:D009062)
- **Chemicals:** triglycerides (MESH:D014280), DMR (-), silicone (MESH:D012828), polyurethane (MESH:D011140), cholesterol (MESH:D002784), glucose (MESH:D005947), Argon (MESH:D001128), resmetirom (MESH:C588408)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

61 references — full list in the complete paper: https://tomesphere.com/paper/PMC12938758/full.md

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Source: https://tomesphere.com/paper/PMC12938758