| Literature DB >> 21180531 |
Gideon M Hirschfield1, Nadya Al-Harthi, E Jenny Heathcote.
Abstract
Therapeutic strategies for autoimmune liver diseases are increasingly established. Although proportionately uncommon, specialist centers have with time refined the best approaches for each disease, based on an improved understanding of the spectrum of presentation. The major treatment aims are to prevent end-stage liver disease and its associated complications. As a result of drugs such as ursodeoxycholic acid, predniso(lo)ne and azathioprine, both primary biliary cirrhosis and autoimmune hepatitis are now less commonly indications for liver transplantation. Unfortunately, the same inroads in treatment efficacy have as yet not been made for primary sclerosing cholangitis, although the recognition that a subset of patients may have a treatable secondary sclerosing cholangitis (IgG4 related) is helping a proportion. With better biological understanding, more specific interventions are expected that will benefit all those with autoimmune liver diseases.Entities:
Keywords: autoimmune hepatitis; autoimmune pancreatitis; primary biliary cirrhosis; primary sclerosing cholangitis; secondary sclerosing cholangitis
Year: 2009 PMID: 21180531 PMCID: PMC3002506 DOI: 10.1177/1756283X08098966
Source DB: PubMed Journal: Therap Adv Gastroenterol ISSN: 1756-283X Impact factor: 4.409