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Description
Purpose of Review 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 RAs)
Frequently asked questions
It mimics the action of the glucagon-like peptide-1 (GLP-1) hormone, which stimulates insulin secretion, inhibits glucagon release, slows gastric emptying, and reduces appetite, leading to better blood sugar control and
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GLP-1 drugs like semaglutide may reduce opioid addiction cravings and overdose risk, according to new research.
