GLP-1 and Glucagon Receptor Dual Agonists in the Management of Metabolic Dysfunction-associated Steatotic Disease (MASLD)
摘要
This review explores the rationale and available evidence behind incretin-based therapies for metabolic dysfunction-associated steatotic disease (MASLD) and metabolic-associated steatohepatitis (MASH), focusing on glucagon-like peptide 1 (GLP-1) and glucagon (GCG) receptor dual agonists (GLP-1/GCG RA’s).
Recent FindingsMASLD is the most prevalent chronic liver disease globally, with its more severe form, MASH, emerging as the leading cause of liver transplantation and hepatocellular carcinoma. However, cardiovascular disease remains the primary cause of mortality in this population. While there is no approved treatment for MASLD in Europe yet, incretin-based therapies are rising as promising option acting at both cardiovascular and hepatic level.
SummaryGLP-1/GCG RA’s have consistently shown a reduction in liver fat content independent of weight loss, positioning them as a promising treatment for MASLD and MASH. However, their approval will depend on histological and clinical outcomes, which rely on the results of ongoing Phase II and III trials.