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Consecutive fecal calprotectin measurements for predicting relapse in pediatric Crohn’s disease patients

BACKGROUND: Asymptomatic children with Crohn’s disease (CD) require ongoing monitoring to ensure early recognition of a disease exacerbation. AIM: In a cohort of pediatric CD patients, we aimed to assess the utility of serial fecal calprotectin measurements to detect intestinal inflammatory activity...

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Autores principales: Foster, Alice Jane, Smyth, Matthew, Lakhani, Alam, Jung, Benjamin, Brant, Rollin F, Jacobson, Kevan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Baishideng Publishing Group Inc 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421242/
https://www.ncbi.nlm.nih.gov/pubmed/30886509
http://dx.doi.org/10.3748/wjg.v25.i10.1266
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author Foster, Alice Jane
Smyth, Matthew
Lakhani, Alam
Jung, Benjamin
Brant, Rollin F
Jacobson, Kevan
author_facet Foster, Alice Jane
Smyth, Matthew
Lakhani, Alam
Jung, Benjamin
Brant, Rollin F
Jacobson, Kevan
author_sort Foster, Alice Jane
collection PubMed
description BACKGROUND: Asymptomatic children with Crohn’s disease (CD) require ongoing monitoring to ensure early recognition of a disease exacerbation. AIM: In a cohort of pediatric CD patients, we aimed to assess the utility of serial fecal calprotectin measurements to detect intestinal inflammatory activity and predict disease relapse. METHODS: In this prospective longitudinal cohort study, children with CD on infliximab therapy in clinical remission were included. Fecal calprotectin levels were assessed at baseline and at subsequent 2-5 visits. Clinical and biochemical disease activity were assessed using the Pediatric Crohn’s Disease Activity Index, C-reactive protein and erythrocyte sedimentation rate at baseline and at visits over the following 18 mo. RESULTS: 53 children were included and eighteen patients (34%) had a clinical disease relapse during the study. Baseline fecal calprotectin levels were higher in patients that developed symptomatic relapse [median (interquartile range), relapse 723 μg/g (283-1758) vs 244 μg/g (61-627), P = 0.02]. Fecal calprotectin levels > 250 μg/g demonstrated good predictive accuracy of a clinical flare within 3 mo (area under the receiver operator curve was 0.86, 95% confidence limits 0.781 to 0.937). CONCLUSION: Routine fecal calprotectin testing in children with CD in clinical remission is useful to predict relapse. Levels > 250 μg/g are a good predictor of relapse in the following 3 mo. This information is important to guide monitoring standards used in this population.
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spelling pubmed-64212422019-03-18 Consecutive fecal calprotectin measurements for predicting relapse in pediatric Crohn’s disease patients Foster, Alice Jane Smyth, Matthew Lakhani, Alam Jung, Benjamin Brant, Rollin F Jacobson, Kevan World J Gastroenterol Observational Study BACKGROUND: Asymptomatic children with Crohn’s disease (CD) require ongoing monitoring to ensure early recognition of a disease exacerbation. AIM: In a cohort of pediatric CD patients, we aimed to assess the utility of serial fecal calprotectin measurements to detect intestinal inflammatory activity and predict disease relapse. METHODS: In this prospective longitudinal cohort study, children with CD on infliximab therapy in clinical remission were included. Fecal calprotectin levels were assessed at baseline and at subsequent 2-5 visits. Clinical and biochemical disease activity were assessed using the Pediatric Crohn’s Disease Activity Index, C-reactive protein and erythrocyte sedimentation rate at baseline and at visits over the following 18 mo. RESULTS: 53 children were included and eighteen patients (34%) had a clinical disease relapse during the study. Baseline fecal calprotectin levels were higher in patients that developed symptomatic relapse [median (interquartile range), relapse 723 μg/g (283-1758) vs 244 μg/g (61-627), P = 0.02]. Fecal calprotectin levels > 250 μg/g demonstrated good predictive accuracy of a clinical flare within 3 mo (area under the receiver operator curve was 0.86, 95% confidence limits 0.781 to 0.937). CONCLUSION: Routine fecal calprotectin testing in children with CD in clinical remission is useful to predict relapse. Levels > 250 μg/g are a good predictor of relapse in the following 3 mo. This information is important to guide monitoring standards used in this population. Baishideng Publishing Group Inc 2019-03-14 2019-03-14 /pmc/articles/PMC6421242/ /pubmed/30886509 http://dx.doi.org/10.3748/wjg.v25.i10.1266 Text en ©The Author(s) 2019. Published by Baishideng Publishing Group Inc. All rights reserved. http://creativecommons.org/licenses/by-nc/4.0/ This article is an open-access article which was selected by an in-house editor and fully peer-reviewed by external reviewers. It is distributed in accordance with the Creative Commons Attribution Non Commercial (CC BY-NC 4.0) license, which permits others to distribute, remix, adapt, build upon this work non-commercially, and license their derivative works on different terms, provided the original work is properly cited and the use is non-commercial.
spellingShingle Observational Study
Foster, Alice Jane
Smyth, Matthew
Lakhani, Alam
Jung, Benjamin
Brant, Rollin F
Jacobson, Kevan
Consecutive fecal calprotectin measurements for predicting relapse in pediatric Crohn’s disease patients
title Consecutive fecal calprotectin measurements for predicting relapse in pediatric Crohn’s disease patients
title_full Consecutive fecal calprotectin measurements for predicting relapse in pediatric Crohn’s disease patients
title_fullStr Consecutive fecal calprotectin measurements for predicting relapse in pediatric Crohn’s disease patients
title_full_unstemmed Consecutive fecal calprotectin measurements for predicting relapse in pediatric Crohn’s disease patients
title_short Consecutive fecal calprotectin measurements for predicting relapse in pediatric Crohn’s disease patients
title_sort consecutive fecal calprotectin measurements for predicting relapse in pediatric crohn’s disease patients
topic Observational Study
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6421242/
https://www.ncbi.nlm.nih.gov/pubmed/30886509
http://dx.doi.org/10.3748/wjg.v25.i10.1266
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