Faecal Calprotectin Predicts Endoscopic and Histological Activity in Clinically Quiescent Ulcerative Colitis.


Journal

Journal of Crohn's & colitis
ISSN: 1876-4479
Titre abrégé: J Crohns Colitis
Pays: England
ID NLM: 101318676

Informations de publication

Date de publication:
01 Jan 2020
Historique:
pubmed: 18 7 2019
medline: 25 7 2020
entrez: 18 7 2019
Statut: ppublish

Résumé

Faecal calprotectin [FC] is a reliable surrogate marker for disease activity in ulcerative colitis [UC]; however, there are no consensus cut-off values for remission. The study aim was to correlate FC with Mayo Endoscopic Score [MES] and histological disease activity of UC patients in clinical remission. Our study recruited adult UC patients at the McGill IBD Center between 2013 and 2017. Patients in clinical remission [partial Mayo score ≤2], undergoing endoscopy for disease activity or dysplasia surveillance, were enrolled. Before bowel preparation, FC was collected. MES was documented during colonoscopy. Biopsies were taken; histological activity was assessed using Geboes score and the presence of basal plasmacytosis. A total of 185 patients were recruited. The area under the curve [AUC] in receiver operating characteristic [ROC] analysis to predict MES 1-3 [from 0] was 0.743 [95% CI 0.67-0.82; p <0.001] with an FC cut-off value 170 µg/g [64% sensitivity, 74% specificity], and to predict MES 2-3 [from 0-1] was 0.722 [95% CI 0.61-0.83; p <0.001] with an FC cut-off value 170 µg/g [69% sensitivity, 65% specificity]. To differentiate MES 0 from MES 1, an FC value 130 µg/g yields a 70% sensitivity and 68% specificity. The AUC in ROC analysis to predict Geboes <3.1 was 0.627 [95% CI 0.55-0.71; p = 0.003], with an FC value 135 µg/g [54% sensitivity, 69% specificity]. In this large study, FC ≥170 µg/g predicts endoscopic activity and FC ≥135 µg/g predicts histological activity. Therefore in clinical practice, lower faecal calprotectin thresholds can be chosen to optimise identification of patients with ongoing endoscopic and histological disease activity.

Identifiants

pubmed: 31314884
pii: 5513281
doi: 10.1093/ecco-jcc/jjz107
doi:

Substances chimiques

Biomarkers 0
Leukocyte L1 Antigen Complex 0

Types de publication

Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

46-52

Informations de copyright

Copyright © 2019 European Crohn’s and Colitis Organisation (ECCO). Published by Oxford University Press. All rights reserved. For permissions, please email: journals.permissions@oup.com.

Auteurs

Lara Hart (L)

Division of Gastroenterology, Department of Medicine, McGill University, Montreal, QC, Canada.

Mallory Chavannes (M)

Division of Gastroenterology, Department of Medicine, University of British Columbia, Vancouver, BC, Canada.

Omar Kherad (O)

Division of Gastroenterology, Department of Medicine, McGill University, Montreal, QC, Canada.
Department of Internal Medicine, Hôpital de la Tour and University of Geneva, Geneva, Switzerland.

Chelsea Maedler (C)

Department of Pathology, McGill University, Montreal, QC, Canada.

Nathalie Mourad (N)

Department of Pathology, McGill University, Montreal, QC, Canada.

Victoria Marcus (V)

Department of Pathology, McGill University, Montreal, QC, Canada.

Waqqas Afif (W)

Division of Gastroenterology, Department of Medicine, McGill University, Montreal, QC, Canada.

Alain Bitton (A)

Division of Gastroenterology, Department of Medicine, McGill University, Montreal, QC, Canada.

Peter L Lakatos (PL)

Division of Gastroenterology, Department of Medicine, McGill University, Montreal, QC, Canada.
Division of Gastroenterology, Department of Medicine, Semmelweis University, Budapest, Hungary.

Paul Brassard (P)

Division of Clinical Epidemiology, Department of Medicine, McGill University, Montreal, QC, Canada.

Talat Bessissow (T)

Division of Gastroenterology, Department of Medicine, McGill University, Montreal, QC, Canada.

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Classifications MeSH