Anti-diabetic medications in MASLD and MASH
Medication | Liver enzymes | Hepatic steatosis | Liver stiffness | MASH | Fibrosis progression | Fibrosis regression |
Tirzepatide71 72 | Beneficial | Beneficial | Beneficial | Beneficial | Possible benefit | Possible benefit |
GLP-1 RA62–66 68 69 | Beneficial | Beneficial | Beneficial | Beneficial | Possible benefit* | Possible benefit* |
Pioglitazone44 46–51 | Beneficial | Beneficial | Beneficial | Beneficial | Possible benefit | Neutral |
SGLT2 inhibitors92–101 | Beneficial | Beneficial | Beneficial | Unknown | Unknown | Unknown |
Insulin102–104 | Beneficial | Beneficial | Unknown | Unknown | Unknown | Unknown |
Metformin105–107 | Beneficial | Neutral | Neutral | Neutral | Neutral | Neutral |
DPP-4 Inhibitors105–107 | Neutral | Unknown | Unknown | Unknown | Unknown | Unknown |
Sulfonylureas13 | Neutral | Unknown | Unknown | Unknown | Unknown | Unknown |
*Histological evidence for semaglutide.68
GLP-1 RA, glucagon-like peptide-1 receptor agonists; MASH, metabolic dysfunction-associated steatohepatitis; MASLD, metabolic dysfunction-associated steatotic liver disease; SGLT2, sodium-glucose transporter 2.