Literature DB >> 23775876

Population-based epidemiology, malignancy risk, and outcome of primary sclerosing cholangitis.

Kirsten Boonstra1, Rinse K Weersma, Karel J van Erpecum, Erik A Rauws, B W Marcel Spanier, Alexander C Poen, Karin M van Nieuwkerk, Joost P Drenth, Ben J Witteman, Hans A Tuynman, Anton H Naber, Paul J Kingma, Henk R van Buuren, Bart van Hoek, Frank P Vleggaar, Nan van Geloven, Ulrich Beuers, Cyriel Y Ponsioen.   

Abstract

UNLABELLED: Extensive population-based studies are much needed to accurately establish epidemiology and disease course in patients with primary sclerosing cholangitis (PSC). We aimed to obtain population-based prevalence and incidence figures, insight in disease course with regard to survival, liver transplantation (LT), and occurrence of malignancies, as well as risk factors thereof. Four independent hospital databases were searched in 44 hospitals in a large geographically defined area of the Netherlands, comprising 50% of the population. In addition, all PSC patients in the three Dutch liver transplant centers and all inflammatory bowel disease (IBD) patients in the adherence area of a large district hospital were identified. All medical records were reviewed on-site, verifying diagnosis. Five hundred and ninety PSC patients were identified, resulting in an incidence of 0.5 and a point prevalence of 6.0 per 100,000. Median follow up was 92 months. Estimated median survival from diagnosis until LT or PSC-related death in the entire cohort was 21.3 years, as opposed to 13.2 years in the combined transplant centers cohort (n = 422; P < 0.0001). Colorectal carcinoma (CRC) risk was 10-fold increased, as compared to ulcerative colitis controls, and developed at a much younger age (39 years; range, 26-64), compared to IBD controls (59 years; range, 34-73; P = 0.019). Colonoscopic surveillance was associated with significantly better outcome.
CONCLUSION: This study exemplifies that, for relatively rare diseases, it is paramount to collect observational data from large, population-based cohorts, because incidence and prevalence rates of PSC are markedly lower and survival much longer than previously reported. The selection of a bias-free, population-based cohort showed a significantly longer survival, compared to the tertiary referral cohort. CRC can develop at an early age, warranting surveillance from time of PSC diagnosis.
© 2013 by the American Association for the Study of Liver Diseases.

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Year:  2013        PMID: 23775876     DOI: 10.1002/hep.26565

Source DB:  PubMed          Journal:  Hepatology        ISSN: 0270-9139            Impact factor:   17.425


  144 in total

1.  Efficacy and safety of curcumin in primary sclerosing cholangitis: an open label pilot study.

Authors:  John E Eaton; Kevin M Nelson; Andrea A Gossard; Elizabeth J Carey; James H Tabibian; Keith D Lindor; Nicholas F LaRusso
Journal:  Scand J Gastroenterol       Date:  2019-05-26       Impact factor: 2.423

2.  Diagnosis, prognosis, and management of primary sclerosing cholangitis.

Authors:  Cyriel Ponsioen
Journal:  Gastroenterol Hepatol (N Y)       Date:  2013-07

Review 3.  Update in the Care and Management of Patients with Primary Sclerosing Cholangitis.

Authors:  Mai Sedki; Cynthia Levy
Journal:  Curr Gastroenterol Rep       Date:  2018-06-09

4.  Liver disease in women: the influence of gender on epidemiology, natural history, and patient outcomes.

Authors:  Jennifer Guy; Marion G Peters
Journal:  Gastroenterol Hepatol (N Y)       Date:  2013-10

Review 5.  The evolution of natural history of primary sclerosing cholangitis.

Authors:  Will R Takakura; James H Tabibian; Christopher L Bowlus
Journal:  Curr Opin Gastroenterol       Date:  2017-03       Impact factor: 3.287

6.  GPR35 promotes glycolysis, proliferation, and oncogenic signaling by engaging with the sodium potassium pump.

Authors:  Georg Schneditz; Joshua E Elias; Ester Pagano; M Zaeem Cader; Svetlana Saveljeva; Kathleen Long; Subhankar Mukhopadhyay; Maryam Arasteh; Trevor D Lawley; Gordon Dougan; Andrew Bassett; Tom H Karlsen; Arthur Kaser; Nicole C Kaneider
Journal:  Sci Signal       Date:  2019-01-01       Impact factor: 8.192

7.  Intrahepatic cystic biliary dilatation constitutes a significant prognostic factor in patients with primary sclerosing cholangitis.

Authors:  Laetitia Nguyen; Nora Cazzagon; Christophe Corpechot; Sanaâ El Mouhadi; Sara Lemoinne; Olivier Chazouillères; Lionel Arrivé
Journal:  Eur Radiol       Date:  2018-08-29       Impact factor: 5.315

Review 8.  Creating an effective clinical registry for rare diseases.

Authors:  Hedwig Ma D'Agnolo; Wietske Kievit; Raul J Andrade; Tom Hemming Karlsen; Heiner Wedemeyer; Joost Ph Drenth
Journal:  United European Gastroenterol J       Date:  2015-11-13       Impact factor: 4.623

Review 9.  Sex-related factors in autoimmune liver diseases.

Authors:  Dorothee Schwinge; Christoph Schramm
Journal:  Semin Immunopathol       Date:  2018-10-01       Impact factor: 9.623

10.  Carcinoembryonic Antigen Level in Primary Sclerosing Cholangitis Is Not Influenced by Dominant Strictures or Bacterial Cholangitis.

Authors:  Andreas Wannhoff; Christian Rupp; Kilian Friedrich; Johannes Knierim; Christa Flechtenmacher; Karl Heinz Weiss; Wolfgang Stremmel; Daniel N Gotthardt
Journal:  Dig Dis Sci       Date:  2016-12-09       Impact factor: 3.199

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