Gut 2007;56:1394-1403
INFLAMMATORY BOWEL DISEASE
New serological markers in inflammatory bowel disease are associated with complicated disease behaviour
1 Department of Gastroenterology, University Hospital Gasthuisberg, Leuven, Belgium
2 Glycominds Ltd, Lod, Israel
3 INOVA Diagnostics Inc, San Diego, CA, USA
4 Department of Applied Mathematics and Computer Science, University Gent, Belgium
Correspondence to:
Professor Séverine Vermeire
Department of Gastroenterology, University Hospital Gasthuisberg, Herestraat 49, B-3000 Leuven, Belgium; severine.vermeire{at}uz.kuleuven.be
Background and aims: Several antibodies have been associated with Crohns disease and are associated with distinct clinical phenotypes. The aim of this study was to determine whether a panel of new antibodies against bacterial peptides and glycans could help in differentiating inflammatory bowel disease (IBD), and whether they were associated with particular clinical manifestations.
Methods: Antibodies against a mannan epitope of Saccharomyces cerevisiae (gASCA), laminaribioside (ALCA), chitobioside (ACCA), mannobioside (AMCA), outer membrane porins (Omp) and the atypical perinuclear antineutrophilic cytoplasmic antibody (pANCA) were tested in serum samples of 1225 IBD patients, 200 healthy controls and 113 patients with non-IBD gastrointestinal inflammation. Antibody responses were correlated with the type of disease and clinical characteristics.
Results: 76% of Crohns disease patients had at least one of the tested antibodies. For differentiation between Crohns disease and ulcerative colitis, the combination of gASCA and pANCA was most accurate. For differentiation between IBD, healthy controls and non-IBD gastrointestinal inflammation, the combination of gASCA, pANCA and ALCA had the best accuracy. Increasing amounts and levels of antibody responses against gASCA, ALCA, ACCA, AMCA and Omp were associated with more complicated disease behaviour (44.7% versus 53.6% versus 71.1% versus 82.0%, p < 0.001), and a higher frequency of Crohns disease-related abdominal surgery (38.5% versus 48.8% versus 60.7% versus 75.4%, p < 0.001).
Conclusions: Using this new panel of serological markers, the number and magnitude of immune responses to different microbial antigens were shown to be associated with the severity of the disease. With regard to the predictive role of serological markers, further prospective longitudinal studies are necessary.
Abbreviations: ACCA, Anti-chitobioside carbohydrate antibody; ALCA, anti-laminaribioside carbohydrate antibody; AMCA, anti-mannobioside carbohydrate antibody; AUC, area under the curve; gASCA, anti-Saccharomyces cerevisiae antibody; IBD, inflammatory bowel disease; Omp, outer membrane porin; pANCA, perinuclear anti-neutrophilic cytoplasmic antibody; ROC, receiver operating characteristic
![]()
CiteULike
Complore
Connotea
Del.icio.us
Digg
Reddit
Technorati What's this?
This article has been cited by other articles:
-
Roggenbuck, D, Hausdorf, G, Martinez-Gamboa, L, Reinhold, D, Buttner, T, Jungblut, P R, Porstmann, T, Laass, M W, Henker, J, Buning, C, Feist, E, Conrad, K
(2009). Identification of GP2, the major zymogen granule membrane glycoprotein, as the autoantigen of pancreatic antibodies in Crohn's disease. Gut
58: 1620-1628
[Abstract] [Full Text] -
Chen, C.-S., Sullivan, S., Anderson, T., Tan, A. C., Alex, P. J., Brant, S. R., Cuffari, C., Bayless, T. M., Talor, M. V., Burek, C. L., Wang, H., Li, R., Datta, L. W., Wu, Y., Winslow, R. L., Zhu, H., Li, X.
(2009). Identification of Novel Serological Biomarkers for Inflammatory Bowel Disease Using Escherichia coli Proteome Chip. Mol. Cell. Proteomics
8: 1765-1776
[Abstract] [Full Text] -
Vermeire, S., Van Assche, G., Rutgeerts, P.
(2009). Genetic analysis to predict prognosis at the onset of Crohn's disease: not yet ready for prime time?. Gut
58: 323-324
[Full Text] -
Sendid, B., Dotan, N., Nseir, S., Savaux, C., Vandewalle, P., Standaert, A., Zerimech, F., Guery, B. P., Dukler, A., Colombel, J. F., Poulain, D.
(2008). Antibodies against Glucan, Chitin, and Saccharomyces cerevisiae Mannan as New Biomarkers of Candida albicans Infection That Complement Tests Based on C. albicans Mannan. CVI
15: 1868-1877
[Abstract] [Full Text]
Register for free content
The full back archive is now available for all BMJ Journals. Institutional subscribers may access the entire archive as part of their subscription. Personal subscribers will also have access to all content when logged in. Non-subscribers who register have free access to all articles published before 2006 right back to volume 1 issue 1. Register here to access the free archive of all BMJ Journals.
Don't forget to sign up for content alerts so you keep up to date with all the articles as they are published.
