Statins, Fibrates, and Other Peroxisome Proliferator-Activated Receptor Agonists for the Treatment of Cholestatic Liver Diseases
- PMID: 33867886
- PMCID: PMC8040906
Statins, Fibrates, and Other Peroxisome Proliferator-Activated Receptor Agonists for the Treatment of Cholestatic Liver Diseases
Abstract
Primary biliary cholangitis (PBC) and primary sclerosing cholangitis (PSC) are autoimmune cholestatic liver diseases that commonly result in the need for liver transplantation. The lack of an effective therapy for PSC remains a largely unmet need in hepatology, and although the majority of patients with PBC will have an adequate response to ursodeoxycholic acid and/or obeticholic acid, there is a need for treatment among patients who do not respond completely to these therapies. Investigations of statins, fibrates, and other peroxisome proliferator-activated receptor (PPAR) agonists suggest clinical benefit with some of these agents. Statins have recently been suggested to improve outcomes in patients with PSC but have not demonstrated benefit in patients with PBC, whereas fibrates and newer PPAR agonists appear to improve biochemical markers linked to better clinical outcomes in patients with PBC. Further research is needed to fully understand the clinical efficacy of these agents in the treatment of PBC and PSC.
Keywords: Primary sclerosing cholangitis; fibrates; peroxisome proliferator-activated receptor agonists; primary biliary cholangitis; statins.
Copyright © 2019, Gastro-Hep Communications, Inc.
Conflict of interest statement
Dr Bowlus has received grant support from Gilead, Intercept Pharmaceuticals, CymaBay Therapeutics, Takeda, NGM Biosciences, GlaxoSmithKline, Bristol-Myers Squibb, TARGET PharmaSolutions, Genkyotex, Allergan, TaiwanJ Pharmaceuticals, Eli Lilly, Novartis, and BiomX, and has consulted for Intercept Pharmaceuticals, GlaxoSmithKline, Gilead, CymaBay Therapeutics, Pliant Therapeutics, and BiomX. Ms Dubrovsky has no relevant conflicts of interest to disclose.
References
-
- Trebicka J, Hennenberg M, Laleman W et al. Atorvastatin lowers portal pressure in cirrhotic rats by inhibition of RhoA/Rho-kinase and activation of endothelial nitric oxide synthase. Hepatology. 2007;46(1):242–253. - PubMed
-
- Stanca CM, Bach N, Allina J, Bodian C, Bodenheimer H, Jr, Odin JA. Atorvastatin does not improve liver biochemistries or Mayo risk score in primary biliary cirrhosis. Dig Dis Sci. 2008;53(7):1988–1993. - PubMed
-
- Wagner M, Halilbasic E, Marschall H-U et al. CAR and PXR agonists stimulate hepatic bile acid and bilirubin detoxification and elimination pathways in mice. Hepatology. 2005;42(2):420–430. - PubMed