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Type 1 Autoimmune Pancreatitis in Europe: Clinical Profile and Response to Treatment

  • Kasper A. Overbeek*
  • , Jakob L. Poulsen
  • , Marco Lanzillotta
  • , Olof Vinge-Holmquist
  • , Peter Macinga
  • , A. Fatih Demirci
  • , Daniko P. Sindhunata
  • , Johanna Backhus
  • , Hana Algül
  • , Jorie Buijs
  • , Philippe Levy
  • , Mariia Kiriukova
  • , Elisabetta Goni
  • , Marcus Hollenbach
  • , Rainer C. Miksch
  • , Lumir Kunovsky
  • , Miroslav Vujasinovic
  • , Sara Nikolic
  • , Luke Dickerson
  • , Michael Hirth
  • Markus F. Neurath, Malte Zumblick, Josephine Vila, Mustafa Jalal, Georg Beyer, Fabian Frost, Silvia Carrara, Zdenek Kala, Petr Jabandziev, Gurhan Sisman, Filiz Akyuz, Gabriele Capurso, Massimo Falconi, Alexander Arlt, Frank P. Vleggaar, Luca Barresi, Bill Greenhalf, L. szló Czakó, Peter Hegyi, Andrew Hopper, Manu K. Nayar, Thomas M. Gress, Francesco Vitali, Alexander Schneider, Chris M. Halloran, Jan Trna, Alexey V. Okhlobystin, Lorenzo Dagna, Djuna L. Cahen, Dmitry Bordin, Vinciane Rebours, Julia Mayerle, Alisan Kahraman, Sebastian Rasch, Emma Culver, Alexander Kleger, Emma Martínez-Moneo, Ola Røkke, Tomas Hucl, S. ren S. Olesen, Marco J. Bruno, Emanuel Della-Torre, Ulrich Beuers, J. -Matthias Löhr, Jonas Rosendahl*, PrescrAIP Study Group
*Corresponding author for this work
  • Erasmus MC
  • Aalborg University
  • Viral Evolution and Transmission Unit, Division of Immunology, Transplantation and Infectious Diseases, IRCCS Ospedale San Raffaele, Milan, Italy
  • University of Oslo
  • Norwegian University of Science and Technology
  • Institute for Clinical and Experimental Medicine
  • Marmara University
  • Ulm University
  • Technical University of Munich
  • Hôpital Beaujon
  • Moscow Clinical Scientific Center
  • Ludwig Maximilian University of Munich
  • Leipzig University
  • University Hospital Olomouc–National eHealth Centre
  • Masaryk University
  • Masaryk Memorial Cancer Institute
  • Karolinska Institutet
  • University of Liverpool
  • Heidelberg University 
  • Friedrich-Alexander University Erlangen-Nürnberg
  • University of Marburg
  • Newcastle upon Tyne Hospitals NHS Foundation Trust
  • University of Sheffield
  • University of Greifswald
  • Humanitas Mater Domini
  • Acibadem Mehmet Ali Aydinlar Universitesi
  • Istanbul University
  • Vita-Salute San Raffaele University
  • Kiel University
  • University of Oldenburg
  • University Medical Center Utrecht
  • IRCCS Istituto Mediterraneo per i Trapianti e Terapie ad Alta Specializzazione (ISMETT) - Palermo
  • University of Pecs
  • Semmelweis University
  • Sechenov First Moscow State Medical University
  • Tver State Medical University
  • University of Duisburg-Essen
  • University of Oxford
  • Biocruces Bizkaia
  • Martin Luther University Halle-Wittenberg

Research output: Contribution to journalArticleAcademicpeer-review

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Abstract

Background & Aims: Autoimmune pancreatitis (AIP) is an immune-mediated disease of the pancreas with distinct pathophysiology and manifestations. Our aims were to characterize type 1 AIP in a large pan-European cohort and study the effectiveness of current treatment regimens. Methods: We retrospectively analyzed adults diagnosed since 2005 with type 1 or not-otherwise-specified AIP in 42 European university hospitals. Type 1 AIP was uniformly diagnosed using specific diagnostic criteria. Patients with type 2 AIP and those who had undergone pancreatic surgery were excluded. The primary end point was complete remission, defined as the absence of clinical symptoms and resolution of the index radiologic pancreatic abnormalities attributed to AIP. Results: We included 735 individuals with AIP (69% male; median age, 57 years; 85% White). Steroid treatment was started in 634 patients, of whom 9 (1%) were lost to follow-up. The remaining 625 had a 79% (496/625) complete, 18% (111/625) partial, and 97% (607/625) cumulative remission rate, whereas 3% (18/625) did not achieve remission. No treatment was given in 95 patients, who had a 61% complete (58/95), 19% partial (18/95), and 80% cumulative (76/95) spontaneous remission rate. Higher (≥0.4 mg/kg/day) corticosteroid doses were no more effective than lower (<0.4 mg/kg/day) doses (odds ratio, 0.428; 95% confidence interval, 0.054–3.387) and neither was a starting dose duration >2 weeks (odds ratio, 0.908; 95% confidence interval, 0.818–1.009). Elevated IgG4 levels were independently associated with a decreased chance of complete remission (odds ratio, 0.639; 95% confidence interval, 0.427–0.955). Relapse occurred in 30% of patients. Relapses within 6 months of remission induction were independent of the steroid-tapering duration, induction treatment duration, and total cumulative dose. Conclusions: Patients with type 1 AIP and elevated IgG4 level may need closer monitoring. For remission induction, a starting dose of 0.4 mg/kg/day for 2 weeks followed by a short taper period seems effective. This study provides no evidence to support more aggressive regimens.
Original languageEnglish
Pages (from-to)994-1004.e10
JournalClinical gastroenterology and hepatology
Volume22
Issue number5
Early online date2024
DOIs
Publication statusPublished - May 2024

Keywords

  • Autoimmune Pancreatitis
  • IgG4-Related Disease
  • IgG4-Related Pancreatitis

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