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Please use this identifier to cite or link to this item: http://hdl.handle.net/1942/2207

Title: Pancreatic autoantibodies in inflammatory bowel disease
Authors: Joossens, S
Vermeire, S
Godefridis, G
Claessens, G
Pierik, M
Hietinck, R
Aerts, R.
Rutgeerts, P
Bossuyt, X
VAN STEEN, Kristel
Issue Date: 2004
Citation: INFLAMMATORY BOWEL DISEASES, 10(6). p. 771-777
Abstract: Background: Autoantibodies against exocrine pancreas (PABs) have been reported to be specific for Crohn's disease (CD), albeit at a low prevalence (30%). We studied PABs in patients with inflammatory bowel disease (IBD), unaffected family members, and control subjects. Methods: A Belgian study cohort of 575 subjects, including 289 IBD patients (CD, 169 patients; ulcerative colitis [UC], 120 patients), 108 unaffected first-degree relatives, 78 subjects with non-IBD gastrointestinal disorders (gastrointestinal control subjects [GIcos]), and 100 healthy control subjects (Hcos), were tested for PAB by a standardized indirect immunofluorescence method. Results: The prevalence of PABs in this study cohort was 32% for CD, 23.3% for UC, and 22.2% for their unaffected family members (all P < 0.001), compared with 1.3% for GIcos and 0% for Hcos. Two staining patterns could be observed: an intracellular pattern (IC); and an extracellular pattern (EC). The EC was significantly more prevalent in CD patients compared with UC patients (P = 0.014), and higher titers of this pattern were found in CD patients (P = 0.01). Both PAB patterns were negatively associated with stricturing disease behavior of CD (P = 0.021). The IC was associated with familial CD (P = 0.0009) and familial UC (P = 0.0003). Conclusions: The prevalence of PAB found in CD patients in this study was similar to that cited in previous reports. In contrast to these reports, we also found an increased prevalence of PABs in patients with UC and in unaffected first-degree relatives of IBD patients. We observed two main staining patterns, both of which were present in IBD and were associated with specific phenotypes of the disease.
Notes: Katholieke Univ Leuven, Univ Hosp Gasthuisberg, Dept Gastroenterol, B-3000 Louvain, Belgium. Katholieke Univ Leuven, Univ Hosp Gasthuisberg, Dept Lab Med, B-3000 Louvain, Belgium. Katholieke Univ Leuven, Univ Hosp Gasthuisberg, Ctr Epidemiol & Human Genet, B-3000 Louvain, Belgium. Limburgs Univ Ctr, Ctr Stat, Diepenbeek, Belgium.Bossuyt, X, Katholieke Univ Leuven, Univ Hosp Gasthuisberg, Dept Lab Med, B-3000 Louvain, Belgium.Xavier.Bossuyt@uz.kuleuven.ac.be
URI: http://hdl.handle.net/1942/2207
DOI: 10.1097/00054725-200411000-00012
ISI #: 000224909600012
ISSN: 1078-0998
Category: A1
Type: Journal Contribution
Validation: ecoom, 2005
Appears in Collections: Research publications

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