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Abstract
Chronic liver diseases (CLDs) are increasingly driven by metabolic dysfunction-associated steatotic liver disease (MASLD) and its inflammatory-fibrotic form (MASH).
- Effective pharmacological therapies to halt or reverse fibrosis progression in MASH are currently lacking.
- Incretin-based therapies, such as glucagon-like peptide-1 receptor agonists (GLP-1 RAs), show promising metabolic and anti-inflammatory effects.
- These therapies may also possess potential antifibrotic activity, making them candidates for treating various CLD phenotypes.
- Current knowledge includes insights into the mechanisms of action of these drugs and their clinical trial outcomes.
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