Skip to main content
. 2024 Sep 28;23:346. doi: 10.1186/s12933-024-02434-5

Table 3.

Evaluation of pharmacotherapies in MASLD

Drugs Mechanisms Effects on MASH Impact on Liver Fibrosis Cardioprotective roles
TZDs Activation of PPAR-γ to improve insulin sensitivity Reduces liver fat, improves liver enzyme levels May reduce the progression of fibrosis Improves IR, lowers CV risk
GLP-1 Receptor Agonists Promotes insulin secretion, suppresses appetite Significantly reduces weight, improves liver function indicators Promotes liver cell regeneration, reduces the risk of fibrosis Has cardiovascular protective effects, lowers the incidence of cardiac events
SGLT-2 Inhibitors Inhibits renal glucose reabsorption, promotes glucosuria Reduces blood glucose, improves body weight Reduces liver fat accumulation, may reduce fibrosis Reduces the risk of heart failure, improves cardiac function
Vitamin E Antioxidant effect, reduces oxidative stress Improves hepatitis and liver fat content Helps alleviate liver fibrosis May improve overall metabolic status
OCA Activates FXR, improves bile acid metabolism, anti-fibrotic May improve liver fat content Significantly inhibits the progression of fibrosis Studies show potential cardiovascular benefits
Resmetirom Selectively activates thyroid hormone receptor β, regulates lipid metabolism Significantly reduces liver fat and inflammation markers May reduce fibrosis, improve liver function May have cardioprotective effects
Survodutide/ Tirzepatide Dual GLP-1 and GIP receptor agonist, promotes weight loss Significantly reduces weight, improves liver function indicators May reduce liver fat and fibrosis May improve cardiovascular health, lower cardiac risk
Pegozafermin Promotes fat metabolism and anti-inflammatory effects, inhibits liver fibrosis Improves liver fat accumulation, significantly reduces liver function abnormal indicators Significantly inhibits the progression of fibrosis May have a positive effect on cardiovascular health

TZDs: thiazolidinediones, PPAR-γ: peroxisome proliferator-activated receptor gamma, IR: insulin resistance, CV risk: cardiovascular risk, GLP-1: glucagon-like peptide-1, MASH: metabolic dysfunction-associated steatohepatitis, SGLT-2: sodium-glucose transporter 2, OCA: obeticholic acid, FXR: farnesoid X receptor, GIP: glucose- dependent insulinotropic polypeptide