MedUni Vienna: Chronic inflammatory liver disease: cell stress mechanisms identified as prognostic factor

International study led by MedUni Vienna appears in "Hepatology"

Primary sclerosing cholangitis (PSC) is a rare, chronic, inflammatory disease of the bile ducts and is difficult to treat, since its causes have not yet been adequately researched. Using RNA sequencing, an international research consortium led by Michael Trauner, Head of MedUni Vienna's Division of Gastroenterology and Hepatology (Department of Medicine III), has now succeeded in identifying a new prognostic factor for PSC from liver biopsies. This is so-called cellular ER stress. ER stress is the name given to a complex cellular response to stress caused by the build-up of misfolded proteins in the endoplasmic reticulum (ER).

PSC is a rare disease with a poor prognosis and can lead to cirrhosis of the liver or bile duct cancer. It affects 0.01% of the population but, even though it is rare, PSC is responsible for more than 10% of all liver transplants, making it the third most common indication on liver transplant waiting lists in Europe.

In the recent study, which has now been published in the leading journal "Hepatology", the researchers were able to identify a molecular signature for ER stress both in the liver cells (hepatocytes) and also in the bile duct epithelium – and notably as a stand-alone factor that is independent of the disease stage or degree of liver fibrosis (laying down of scar tissue) as a precursor to possible liver cirrhosis. "Using transcriptional analysis, we were able to identify a personalised molecular signature of primary sclerosing cholangitis, which shows that patients with an impaired response to ER stress have a poorer prognosis with a higher incidence of complications," explains Trauner. "This discovery also opens up new treatment options, since ER stress can be counteracted with drugs."  

Since the build-up of potentially toxic bile acids in cholestasis results in ER stress, it is now being attempted to restore this balance pharmacologically using the new bile acid therapeutics that are available. Beneficial effects can reportedly be expected from drugs already in clinically testing – however, more research has already been initiated to explore this further.  

MedUni Vienna a world-leading hepatology centre

The international study was conducted under the lead of of MedUni Vienna, working with teams from the USA (Fairfax Hospital; Feinberg School of Medicine, Chicago; University of Miami; Liver Institute Northwest, Seattle; University of California at Davis, Sacramento; Duke University School of Medicine, Durham) and Canada (University of Alberta, Edmonton) in collaboration with Gilead Sciences and the biopsies were enabled by a clinical trial conducted by Gilead. MedUni Vienna's Division of Gastroenterology and Hepatology is regarded as one of the world’s leading centres for research into primary sclerosing cholangitis (PSC), non-alcoholic fatty liver disease (NAFLD) and bile acid metabolism disorders in liver and biliary tract disease. Currently, one of MedUni Vienna's main research interests in the Immunology Research Cluster is immunometabolism, which is concerned with the interaction between immunologic and metabolic processes.

Service: Hepatology

"A Fibrosis-Independent Hepatic Transcriptomic Signature Identifies Drivers of Disease Progression in Primary Sclerosing Cholangitis." Yevgeniy Gindin, Chuhan Chung, Zhaoshi Jiang, Jing Zhu Zhou, Jun Xu, Andrew N. Billin, Robert P. Myers, Zachary Goodman, Abdolamir Landi, Michael Houghton, Richard M. Green, Cynthia Levy, Kris V. Kowdley, Christopher L. Bowlus, Andrew J. Muir and Michael Trauner. Link:

The sender takes full responsibility for the content of this news item. Content may include forward-looking statements which, at the time they were made, were based on expectations of future events. Readers are cautioned not to rely on these forward-looking statements.

As a life sciences organization based in Vienna, would you like us to promote your news and events? If so, please send your contributions to news(at)