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This review examines the biological mechanisms underlying GLP-1 RA therapy in MASLD/MASH, analyzes the mechanistic distinctions between mono-, dual-, and triple agonists, and synthesizes current clinical evidence supporting their utilization in individuals with this condition.
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The explosive demand for GLP-1 (glucagon-like peptide-1) receptor agonists, driven by their efficacy in treating obesity, has outpaced supply and created a dynamic market landscape

can they fix India's thin-fat crisis shaped by metabolism, muscle, diet, and genes?
