Variation of faecal calprotectin level within the first three months after bowel resection is predictive of endoscopic postoperative recurrence in Crohn's disease.


Journal

Digestive and liver disease : official journal of the Italian Society of Gastroenterology and the Italian Association for the Study of the Liver
ISSN: 1878-3562
Titre abrégé: Dig Liver Dis
Pays: Netherlands
ID NLM: 100958385

Informations de publication

Date de publication:
07 2020
Historique:
received: 14 01 2020
revised: 18 03 2020
accepted: 23 03 2020
pubmed: 24 5 2020
medline: 20 7 2021
entrez: 24 5 2020
Statut: ppublish

Résumé

Early prediction of postoperative recurrence (POR) remains a major concern in Crohn's disease (CD). To assess serial faecal calprotectin (Fcal) monitoring within the first three months to predict CD endoscopic POR. In a multicenter randomized controlled trial, CD patients received azathioprine 2.5 mg/kg/day with oral curcumin (3 g/day) or placebo. Fcal was measured at baseline, one month (M1) and M3. Endoscopic POR at M6 was defined as Rutgeerts' index ≥ i2b (central reading). Among the 48 patients included, there was no significant difference of median Fcal levels at baseline (p = 0.15), M1 (p = 0.44) and M3 (p = 0.28) between patients with or without endoscopic POR at M6. Fcal kinetics during the first 3 months after surgery was significantly different between the patients with or without POR at M6 (p = 0.021). The median variation between Fcal level at baseline and M3 (ΔFcal M3-M0) was significantly higher in patients with endoscopic POR compared to those without POR (p = 0.01). ΔFcal M3-M0 >+10% demonstrated the best performances to predict endoscopic POR at M6 (AUC=0.73, sensitivity=64.7%[41.1-82.7], specificity=87.5%[68.0-96.3], negative predictive value=77.8%[57.5-91.4] and positive predictive value=78.6%[49.2-95.3]). Fcal variation within the first three months after ileocolonic resection is a promising predictor of early endoscopic POR in CD patients.

Sections du résumé

BACKGROUND
Early prediction of postoperative recurrence (POR) remains a major concern in Crohn's disease (CD).
AIMS
To assess serial faecal calprotectin (Fcal) monitoring within the first three months to predict CD endoscopic POR.
METHODS
In a multicenter randomized controlled trial, CD patients received azathioprine 2.5 mg/kg/day with oral curcumin (3 g/day) or placebo. Fcal was measured at baseline, one month (M1) and M3. Endoscopic POR at M6 was defined as Rutgeerts' index ≥ i2b (central reading).
RESULTS
Among the 48 patients included, there was no significant difference of median Fcal levels at baseline (p = 0.15), M1 (p = 0.44) and M3 (p = 0.28) between patients with or without endoscopic POR at M6. Fcal kinetics during the first 3 months after surgery was significantly different between the patients with or without POR at M6 (p = 0.021). The median variation between Fcal level at baseline and M3 (ΔFcal M3-M0) was significantly higher in patients with endoscopic POR compared to those without POR (p = 0.01). ΔFcal M3-M0 >+10% demonstrated the best performances to predict endoscopic POR at M6 (AUC=0.73, sensitivity=64.7%[41.1-82.7], specificity=87.5%[68.0-96.3], negative predictive value=77.8%[57.5-91.4] and positive predictive value=78.6%[49.2-95.3]).
CONCLUSION
Fcal variation within the first three months after ileocolonic resection is a promising predictor of early endoscopic POR in CD patients.

Identifiants

pubmed: 32444250
pii: S1590-8658(20)30122-5
doi: 10.1016/j.dld.2020.03.020
pii:
doi:

Substances chimiques

Anti-Inflammatory Agents, Non-Steroidal 0
Biomarkers 0
Immunosuppressive Agents 0
Leukocyte L1 Antigen Complex 0
Curcumin IT942ZTH98
Azathioprine MRK240IY2L

Types de publication

Clinical Trial, Phase III Journal Article Multicenter Study Randomized Controlled Trial Research Support, Non-U.S. Gov't

Langues

eng

Sous-ensembles de citation

IM

Pagination

740-744

Informations de copyright

Copyright © 2020 Editrice Gastroenterologica Italiana S.r.l. Published by Elsevier Ltd. All rights reserved.

Auteurs

Mathilde Boube (M)

Université Clermont Auvergne, Inserm, 3iHP, CHU Clermont-Ferrand, Service d'Hépato-Gastro Entérologie, Clermont-Ferrand, France; Université Clermont Auvergne, Inserm U1071, M2iSH, USC-INRA 2018, F-63000 Clermont-Ferrand, France.

David Laharie (D)

Gastroenterology Department, University Hospital, Bordeaux, France.

Stéphane Nancey (S)

Hospices Civils de Lyon, Lyon-Sud hospital, Gastroenterology, Pierre Benite, France.

Xavier Hebuterne (X)

Department of Gastroenterology and Clinical Nutrition, CHU of Nice and University of Nice Sophia-Antipolis, Nice, France.

Mathurin Fumery (M)

Gastroenterology Department, University Hospital, Amiens, France.

Benjamin Pariente (B)

Gastroenterology Department, University Hospital, Lille, France.

Xavier Roblin (X)

Gastroenterology Department, University Hospital, Saint-Etienne, France.

Laurent Peyrin-Biroulet (L)

Department of Gastroenterology, CHU Nancy Brabois, Vandoeuvre les Nancy, France.

Régine Minet-Quinard (R)

CHU Clermont-Ferrand, Laboratoire de Biochimie, Université Clermont Auvergne, Clermont-Ferrand, France.

Bruno Pereira (B)

CHU Clermont-Ferrand, DRCI, Unité de Biostatistiques, Université Clermont Auvergne, Clermont-Ferrand, France.

Gilles Bommelaer (G)

Université Clermont Auvergne, Inserm, 3iHP, CHU Clermont-Ferrand, Service d'Hépato-Gastro Entérologie, Clermont-Ferrand, France; Université Clermont Auvergne, Inserm U1071, M2iSH, USC-INRA 2018, F-63000 Clermont-Ferrand, France.

Anthony Buisson (A)

Université Clermont Auvergne, Inserm, 3iHP, CHU Clermont-Ferrand, Service d'Hépato-Gastro Entérologie, Clermont-Ferrand, France; Université Clermont Auvergne, Inserm U1071, M2iSH, USC-INRA 2018, F-63000 Clermont-Ferrand, France. Electronic address: a_buisson@hotmail.fr.

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Classifications MeSH