Discovery of biomarker candidates associated with the risk of short-term and mid/long-term relapse after infliximab withdrawal in Crohn's patients: a proteomics-based study.

Crohn's disease IBD clinical clinical decision making inflammatory bowel disease infliximab

Journal

Gut
ISSN: 1468-3288
Titre abrégé: Gut
Pays: England
ID NLM: 2985108R

Informations de publication

Date de publication:
26 Oct 2020
Historique:
received: 10 06 2020
revised: 30 09 2020
accepted: 02 10 2020
entrez: 27 10 2020
pubmed: 28 10 2020
medline: 28 10 2020
Statut: aheadofprint

Résumé

A subset of Crohn's disease (CD) patients experiences mid/long-term remission after infliximab withdrawal. Biomarkers are needed to identify those patients. New biomarkers of relapse were searched in the baseline serum of CD patients stopping infliximab when they were under combined therapy (antimetabolite and infliximab) and stable clinical remission (diSconTinuation in CrOhn's disease patients in stable Remission on combined therapy with Immunosuppressors cohort, n=102). From shotgun proteomics experiment (discovery step), biomarker candidates were identified and further targeted by selected reaction monitoring (verification step). The dataset was stratified to search for markers of short-term (<6 months) or mid/long-term relapse (>6 months). The risk of relapse and the predicting capacity associated with biomarker candidates were evaluated using univariate Cox model and log-rank statistic, respectively. To test their complementary predicting capacity, biomarker candidates were systematically combined in pairs. Distinct biomarker candidates were associated with the risk (HR) of short-term (15 proteins, 2.9<HR<16.1, p<0.05) and mid/long-term (17 proteins, 2.1<HR<4.7, p<0.05) relapse, they reflect different pathophysiological processes. In stratified and non-stratified datasets, novel marker combinations exhibited a high predicting capacity as shown by their higher Z-scores (false discovery rate <0.001) than C reactive protein and faecal calprotectin (current references in predicting relapse). We identified for the first time circulating biomarker candidates associated with the risk of mid/long-term relapse in CD patients stopping infliximab. We also highlight a sequence of pathophysiological processes leading to relapse, this could help to better understand the disease progression. Our findings may pave the way for a better non-invasive evaluation of the risk of relapse when contemplating antitumour necrosis factor α withdrawal in CD patients.

Identifiants

pubmed: 33106355
pii: gutjnl-2020-322100
doi: 10.1136/gutjnl-2020-322100
pii:
doi:

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Informations de copyright

© Author(s) (or their employer(s)) 2020. No commercial re-use. See rights and permissions. Published by BMJ.

Déclaration de conflit d'intérêts

Competing interests: None declared.

Auteurs

Nicolas Pierre (N)

Laboratory of Translational Gastroenterology, GIGA-Institute, Liege University, Liege, Belgium nicolas.pierre@uliege.be.

Dominique Baiwir (D)

GIGA Proteomics Facility, Liege University, Liege, Belgium.

Vân Anh Huynh-Thu (VA)

Department of Electrical Engineering and Computer Science, Liege University, Liege, Belgium.

Gabriel Mazzucchelli (G)

Laboratory of Mass Spectrometry, MolSys Research Unit, Liege University, Liege, Belgium.

Nicolas Smargiasso (N)

Laboratory of Mass Spectrometry, MolSys Research Unit, Liege University, Liege, Belgium.

Edwin De Pauw (E)

Laboratory of Mass Spectrometry, MolSys Research Unit, Liege University, Liege, Belgium.

Yoram Bouhnik (Y)

Service de Gastroentérologie et Assistance Nutritive, Hôpital Beaujon, Clichy, France.

David Laharie (D)

Service d'Hépato-Gastroentérologie, CHU de Bordeaux, Bordeaux, France.

Jean-Frédéric Colombel (JF)

Division of Gastroenterology, Icahn School of Medicine at Mount Sina, New York, New York, USA.

Marie-Alice Meuwis (MA)

Laboratory of Translational Gastroenterology, GIGA-Institute, Liege University, Liege, Belgium.
Hepato-Gastroenterology and Digestive Oncology Department, Liege University, Liege, Belgium.

Edouard Louis (E)

Laboratory of Translational Gastroenterology, GIGA-Institute, Liege University, Liege, Belgium.
Hepato-Gastroenterology and Digestive Oncology Department, Liege University, Liege, Belgium.

Classifications MeSH