# Management of obesity in advanced chronic liver disease

**Authors:** Cyrielle Caussy, Sven M. Francque

PMC · DOI: 10.1016/j.jhepr.2026.101749 · JHEP Reports · 2026-01-30

## TL;DR

This paper discusses how obesity affects advanced liver disease and explores new treatment options like lifestyle changes, medications, and surgery.

## Contribution

The paper highlights recent anti-obesity medications as new tools for personalized treatment in patients with obesity and liver disease.

## Key findings

- Obesity is increasingly common in patients with advanced chronic liver disease.
- Higher BMI worsens liver disease outcomes regardless of the cause.
- New anti-obesity medications offer promising treatment options alongside lifestyle and surgical interventions.

## Abstract

Obesity has emerged as a major global health challenge and is closely associated with metabolic dysfunction-associated steatotic liver disease (MASLD) and metabolic dysfunction- and alcohol-associated liver disease (MetALD). Overall, an increased prevalence of obesity has been reported in patients with advanced chronic liver disease (ACLD), in whom it adversely impacts prognosis. Importantly, increased BMI is recognised as a modifiable risk factor for progression of liver disease, regardless of aetiology. The recent approval of effective and well-tolerated anti-obesity medications offers new opportunities, alongside therapeutic lifestyle changes and bariatric surgery, for the personalised management of patients living with obesity and associated liver disease.

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## Linked entities

- **Diseases:** obesity (MONDO:0011122), metabolic dysfunction-associated steatotic liver disease (MONDO:0013209), metabolic dysfunction- and alcohol-associated liver disease (MONDO:0957896)

## Full-text entities

- **Genes:** DPP4 (dipeptidyl peptidase 4) [NCBI Gene 1803] {aka ADABP, ADCP2, CD26, DPPIV, TP103}, INS (insulin) [NCBI Gene 3630] {aka IDDM, IDDM1, IDDM2, ILPR, IRDN, MODY10}, 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}, GIP (gastric inhibitory polypeptide) [NCBI Gene 2695]
- **Diseases:** CSPH (MESH:D006975), ascites (MESH:D001201), acute-on-chronic liver failure (MESH:D065290), malnutrition (MESH:D044342), BS (MESH:D000267), death (MESH:D003643), malabsorption (MESH:D008286), hypertension (MESH:D006973), MALOs (MESH:D011248), viral hepatitis (MESH:D014777), CV (MESH:D002318), Weight loss (MESH:D015431), vascular (MESH:D057772), insulin resistance (MESH:D007333), MetALD (MESH:D008108), obstructive sleep apnoea (MESH:D020181), T2D (MESH:D003924), kidney disease (MESH:D007674), adipose tissue dysfunction (MESH:D018205), HF (MESH:D006333), muscle loss (MESH:D009135), hepatic encephalopathy (MESH:D006501), HCC (MESH:D006528), Chronic inflammation (MESH:D007249), cACLD (MESH:D008107), sarcopenia (MESH:D055948), metabolic syndrome (MESH:D024821), cirrhosis (MESH:D005355), mitochondrial dysfunction (MESH:D028361), alcohol use disorder (MESH:D000437), NAFLD (MESH:D065626), kidney failure (MESH:D051437), liver fibrosis (MESH:D008103), CKD (MESH:D051436), hepatitis B (MESH:D006509), OSA (MESH:C535586), MASH (MESH:D005234), Obesity (MESH:D009765), weight regain (MESH:D055191), Cardiomyopathy (MESH:D009202), carcinogenesis (MESH:D063646), overweight (MESH:D050177), metabolic dysfunction (MESH:D008659), ischaemia (MESH:D007511)
- **Chemicals:** AOM (-), orlistat (MESH:D000077403), naltrexone (MESH:D009271), RAs (MESH:D011883), lipid (MESH:D008055), dopamine (MESH:D004298), topiramate (MESH:D000077236), alcohol (MESH:D000438), serotonin (MESH:D012701), glucose (MESH:D005947), bupropion (MESH:D016642), phentermine (MESH:D010645), free fatty acids (MESH:D005230), norepinephrine (MESH:D009638)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

3 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12969633/full.md

## References

124 references — full list in the complete paper: https://tomesphere.com/paper/PMC12969633/full.md

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Source: https://tomesphere.com/paper/PMC12969633