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Jayasekera, Channa R

0000-0003-4579-840X

Mayo Clinic

Department of Gastroenterology and Hepatology, Mayo Clinic, Phoenix, AZ 85259, USA.

Citations 1

Resmetirom in the Management of Metabolic Dysfunction-Associated Steatotic Liver Disease and Steatohepatitis
Jamal, Fares , Elshaer, Amani , Odeh, Nour B., Alatout, Mayar H., Shahin, Tala, Worden, Astin R., Albunni, Hashem , Jayasekera, Channa R. , Chascsa, David M. , Vargas, Hugo E. , Aqel, Bashar , Albunni, Hashem N , Lizaola-Mayo, Blanca C, Jayasekera, Channa R , Chascsa, David M H, Aqel, Bashar A. , Vargas, Hugo E , Jamal, Fares , Lizaola‐Mayo, Blanca

Life | August 18, 2025 | Volume: 15 | Issue: 8 | Pages: 1306

10.3390/life15081306 Get It

Metabolic dysfunction-associated steatotic liver disease (MASLD) and its progressive form, metabolic dysfunction-associated steatohepatitis (MASH), are among the most prevalent causes of chronic liver disease worldwide, closely linked to the global rise in overweight and obesity, type 2 diabetes, and metabolic syndrome. Until recently, treatment options were limited to lifestyle interventions, with no approved pharmacologic therapies. Resmetirom, a liver-directed, selective thyroid hormone receptor beta (THR-β) agonist, is a promising disease-modifying agent that targets hepatic lipid metabolism, inflammation, and fibrosis. Clinical trials, including the pivotal phase 3 MAESTRO-NASH and MAESTRO-NAFLD-1 trials, have demonstrated significant improvements in liver fat reduction, lipid profiles, histological endpoints, and health-related quality of life, with a favorable safety profile. In March 2024, the FDA granted accelerated approval of resmetirom for adults with MASH and moderate-to-advanced fibrosis, marking a significant milestone in MASLD treatment. This review discusses the mechanistic rationale, preclinical data, and pivotal clinical trial outcomes supporting resmetirom’s role in MASLD/MASH management, while outlining ongoing research needs, including long-term safety, pediatric evaluation, and biomarker development for optimized patient selection.