Abstract
Primary biliary cholangitis, formerly known as primary biliary cirrhosis, is a chronic, autoimmune, and cholestatic disease ameliorating the biliary epithelial system causing fibrosis and end-stage liver disease, over time. Patients range from an asymptomatic phase early in the disease course, to symp-toms of decompensated cirrhosis later in its course. This review focuses on the current consensus on the epidemiology, diagnosis, and management of patients with primary biliary cholangitis. We also discuss established medical management as well as novel and investigational therapeutics in the pipeline for management of PBC.
Original language | English (US) |
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Pages (from-to) | 49-60 |
Number of pages | 12 |
Journal | Journal of Clinical and Translational Hepatology |
Volume | 8 |
Issue number | 1 |
DOIs | |
State | Published - 2020 |
Externally published | Yes |
Keywords
- Epidemiology
- Obeticholic acid
- Primary biliary cholangitis (PBC)
- Treatment
- UDCA
ASJC Scopus subject areas
- Gastroenterology