Table 4.
Treatment | Mechanism of action | Indications and evidence |
---|---|---|
Statins | Improve endothelial function; anti-inflammatory | Emerging evidence suggests potential benefits in portal hypertension and liver fibrosis management |
Human Serum Albumin (HSA) | Oncotic and non-oncotic properties | Reduces renal failure and mortality in spontaneous bacterial peritonitis, type 1 HRS, and paracentesis-induced circulatory dysfunction; prolongs survival in uncomplicated ascites with diuretics |
S-Adenosylmethionine (SAM) | Methyl donor in all methylation reactions and regulates glutathione synthesis | Did not outperform placebo in treating ALD, suggesting abstinence as a more effective liver function improvement method; currently Phase 2 trial underway |
Caffeine/coffee | Antagonizes A2a adenosine receptor; anti-fibrotic | Inverse dose–response relationship with cirrhosis risk; associated with lower liver stiffness and reduced HCC risk |
Alcohol cessation interventions | Reduce liver injury | Critical for alcohol-related liver disease; includes behavioral and pharmacotherapy (e.g. naltrexone) |
Dietary and lifestyle modifications | Improve overall liver health | Sodium restriction for ascites, nutrition for malnutrition, and exercise to reduce sarcopenia |
AC = alcohol-associated cirrhosis.