Literature DB >> 35068791

Diagnosis of Primary Sclerosing Cholangitis Beyond Childhood is Associated with Worse Outcomes.

Stefani Tica1, Saad Alghamdi2, Christopher Tait2, Bonsa Nemera1, Yumirle Turmelle1,2, Jaquelyn Fleckenstein2, Janis Stoll1, Sakil Kulkarni1.   

Abstract

BACKGROUND: The elucidation of differences between adult and pediatric-onset primary sclerosing cholangitis (PSC) may inform clinical decision making, and whether results of adult PSC clinical trials can be extrapolated to pediatric subjects.
METHODS: A single-center retrospective analysis of PSC subjects diagnosed during the epoch 2000-13 was conducted. Demographic, clinical, and laboratory data were compared between PSC subjects diagnosed between 0-18 (pediatric) and 19+ (adult) years of age. An adverse outcome was defined as PSC-related death, liver transplant, or malignancy. Survival without any of these was defined as event-free survival.
RESULTS: Analyses of 28 pediatric-diagnosed and 59 adult-diagnosed subjects revealed that incidence of early portal hypertension (PHT; P = 0.2), laboratory parameters of liver disease severity, and fibrosis grade at diagnosis were comparable between adult and pediatric PSC subjects. Adult-diagnosed PSC subjects had higher incidences of adverse outcomes compared to pediatric-diagnosed PSC subjects (P = 0.02). The age group 0-18 years (n = 30) had significantly better event-free survival compared to the age group more than 40 years (n = 25; P = 0.03). The prevalence of PHT in adult PSC subjects was 2.6 that of pediatric PSC subjects. PHT adversely affected outcomes in both adult (P < 0.001) and pediatric (P = 0.01) subjects. Adult PSC subjects were more likely to develop biliary complications (BCs; P = 0.001), ascites (P = 0.004), and variceal bleed (P = 0.03). Adult PSC subjects were more likely to have extra-hepatic co-morbidities (P < 0.001). Adult subjects had a longer follow-up duration compared to pediatric subjects (P = 0.06).
CONCLUSION: Despite having a comparable clinical, laboratory, and histologic biomarkers of liver disease severity at the time of diagnosis, adult PSC subjects had a worse outcome compared to pediatric PSC subjects. Possible reasons for this finding include higher incidence of PHT, BCs, extra-hepatic co-morbidities, and longer duration of follow-up.
© 2021 Indian National Association for Study of the Liver. Published by Elsevier B.V. All rights reserved.

Entities:  

Keywords:  AIH, autoimmune hepatitis; ALP, alkaline phosphatase; ALT, alanine aminotransferase; AST, aspartate aminotransferase; ERCP, endoscopic cholangiopancreatography; GGT, gamma-glutamyl transferase; GI, gastrointestinal; IBD, inflammatory bowel disease; INR, international normalized ratio; MR imaging, magnetic resonance imaging; MRCP, magnetic resonance cholangiopancreatography; PHT, portal hypertension; PSC, primary sclerosing cholangitis; age; cholangitis; outcome; primary; sclerosing; x ULN, times upper limit of normal

Year:  2021        PMID: 35068791      PMCID: PMC8766535          DOI: 10.1016/j.jceh.2021.03.006

Source DB:  PubMed          Journal:  J Clin Exp Hepatol        ISSN: 0973-6883


  29 in total

1.  Small studies: strengths and limitations.

Authors:  A Hackshaw
Journal:  Eur Respir J       Date:  2008-11       Impact factor: 16.671

2.  Patient Age, Sex, and Inflammatory Bowel Disease Phenotype Associate With Course of Primary Sclerosing Cholangitis.

Authors:  Tobias J Weismüller; Palak J Trivedi; Annika Bergquist; Mohamad Imam; Henrike Lenzen; Cyriel Y Ponsioen; Kristian Holm; Daniel Gotthardt; Martti A Färkkilä; Hanns-Ulrich Marschall; Douglas Thorburn; Rinse K Weersma; Johan Fevery; Tobias Mueller; Olivier Chazouillères; Kornelius Schulze; Konstantinos N Lazaridis; Sven Almer; Stephen P Pereira; Cynthia Levy; Andrew Mason; Sigrid Naess; Christopher L Bowlus; Annarosa Floreani; Emina Halilbasic; Kidist K Yimam; Piotr Milkiewicz; Ulrich Beuers; Dep K Huynh; Albert Pares; Christine N Manser; George N Dalekos; Bertus Eksteen; Pietro Invernizzi; Christoph P Berg; Gabi I Kirchner; Christoph Sarrazin; Vincent Zimmer; Luca Fabris; Felix Braun; Marco Marzioni; Brian D Juran; Karouk Said; Christian Rupp; Kalle Jokelainen; Maria Benito de Valle; Francesca Saffioti; Angela Cheung; Michael Trauner; Christoph Schramm; Roger W Chapman; Tom H Karlsen; Erik Schrumpf; Christian P Strassburg; Michael P Manns; Keith D Lindor; Gideon M Hirschfield; Bettina E Hansen; Kirsten M Boberg
Journal:  Gastroenterology       Date:  2017-03-06       Impact factor: 22.682

3.  Validation, clinical utility and limitations of the Amsterdam-Oxford model for primary sclerosing cholangitis.

Authors:  Jorn C Goet; Annarosa Floreani; Xavier Verhelst; Nora Cazzagon; Lisa Perini; Willem J Lammers; Annemarie C de Vries; Adriaan J van der Meer; Henk R van Buuren; Bettina E Hansen
Journal:  J Hepatol       Date:  2019-07-03       Impact factor: 25.083

4.  Ursodeoxycholic Acid Therapy in Pediatric Primary Sclerosing Cholangitis: Predictors of Gamma Glutamyltransferase Normalization and Favorable Clinical Course.

Authors:  Mark Deneau; Emily Perito; Amanda Ricciuto; Nitika Gupta; Binita M Kamath; Sirish Palle; Bernadette Vitola; Vratislav Smolka; Federica Ferrari; Achiya Z Amir; Tamir Miloh; Alexandra Papadopoulou; Parvathi Mohan; Cara Mack; Kaija-Leena Kolho; Raffaele Iorio; Wael El-Matary; Veena Venkat; Albert Chan; Lawrence Saubermann; Pamela L Valentino; Uzma Shah; Alexander Miethke; Henry Lin; M K Jensen
Journal:  J Pediatr       Date:  2019-03-14       Impact factor: 4.406

5.  Time-dependent Cox regression model is superior in prediction of prognosis in primary sclerosing cholangitis.

Authors:  Kirsten Muri Boberg; Giuseppe Rocca; Thore Egeland; Annika Bergquist; Ulrika Broomé; Llorenc Caballeria; Roger Chapman; Rolf Hultcrantz; Stephen Mitchell; Albert Pares; Floriano Rosina; Erik Schrumpf
Journal:  Hepatology       Date:  2002-03       Impact factor: 17.425

6.  Incidence, clinical spectrum, and outcomes of primary sclerosing cholangitis in a United States community.

Authors:  Kiran Bambha; W Ray Kim; Jayant Talwalkar; Heidi Torgerson; Joanne T Benson; Terry M Therneau; Edward V Loftus; Barbara P Yawn; E Rolland Dickson; L Joseph Melton
Journal:  Gastroenterology       Date:  2003-11       Impact factor: 22.682

Review 7.  Primary sclerosing cholangitis.

Authors:  Jessica K Dyson; Ulrich Beuers; David E J Jones; Ansgar W Lohse; Mark Hudson
Journal:  Lancet       Date:  2018-02-13       Impact factor: 79.321

8.  The natural history of small-duct primary sclerosing cholangitis.

Authors:  Einar Björnsson; Rolf Olsson; Annika Bergquist; Stefan Lindgren; Barbara Braden; Roger W Chapman; Kirsten M Boberg; Paul Angulo
Journal:  Gastroenterology       Date:  2008-01-17       Impact factor: 22.682

9.  Factors Associated With Outcomes of Patients With Primary Sclerosing Cholangitis and Development and Validation of a Risk Scoring System.

Authors:  Elizabeth C Goode; Allan B Clark; George F Mells; Brijesh Srivastava; Kelly Spiess; William T H Gelson; Palak J Trivedi; Kate D Lynch; Edit Castren; Mette N Vesterhus; Tom H Karlsen; Sun-Gou Ji; Carl A Anderson; Douglas Thorburn; Mark Hudson; Michael A Heneghan; Mark A Aldersley; Andrew Bathgate; Richard N Sandford; Graeme J Alexander; Roger W Chapman; Martine Walmsley; Gideon M Hirschfield; Simon M Rushbrook
Journal:  Hepatology       Date:  2019-03-04       Impact factor: 17.425

10.  Impact of age at diagnosis on disease progression in patients with primary sclerosing cholangitis.

Authors:  Christian Rupp; Alexander Rössler; Taotao Zhou; Conrad Rauber; Kilian Friedrich; Andreas Wannhoff; Karl-Heinz Weiss; Peter Sauer; Peter Schirmacher; Caner Süsal; Wolfgang Stremmel; Daniel N Gotthardt
Journal:  United European Gastroenterol J       Date:  2017-06-17       Impact factor: 4.623

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