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Clinical value of serum eosinophilic cationic protein assessment in children with inflammatory bowel disease

INTRODUCTION: Eosinophils contribute to the pathogenesis of inflammatory bowel disease (IBD) in the intestine. Eosinophilic cationic protein (ECP) is one of the most important eosinophilic specific mediators released during activation. The aim of the study was to evaluate the clinical value of serum...

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Autores principales: Wędrychowicz, Andrzej, Tomasik, Przemysław, Pieczarkowski, Stanisław, Kowalska-Duplaga, Kinga, Grzenda-Adamek, Zofia, Fyderek, Krzysztof
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Termedia Publishing House 2013
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296054/
https://www.ncbi.nlm.nih.gov/pubmed/25624851
http://dx.doi.org/10.5114/aoms.2013.34415
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author Wędrychowicz, Andrzej
Tomasik, Przemysław
Pieczarkowski, Stanisław
Kowalska-Duplaga, Kinga
Grzenda-Adamek, Zofia
Fyderek, Krzysztof
author_facet Wędrychowicz, Andrzej
Tomasik, Przemysław
Pieczarkowski, Stanisław
Kowalska-Duplaga, Kinga
Grzenda-Adamek, Zofia
Fyderek, Krzysztof
author_sort Wędrychowicz, Andrzej
collection PubMed
description INTRODUCTION: Eosinophils contribute to the pathogenesis of inflammatory bowel disease (IBD) in the intestine. Eosinophilic cationic protein (ECP) is one of the most important eosinophilic specific mediators released during activation. The aim of the study was to evaluate the clinical value of serum ECP determination in children with active and inactive IBD and its correlation with disease activity. MATERIAL AND METHODS: There were 125 children with IBD (63 with Crohn's disease – CD, 44 with ulcerative colitis – UC, 18 indeterminate colitis – IC) enrolled in the study. Among them 83 children were in the active phase of the disease, while the remaining 42 were in remission. The control group consisted of 56 healthy children. The ECP was assessed three times in children with active IBD, at baseline and after 2 and 6 weeks of treatment and once in children with inactive IBD and controls using fluoroenzymeimmunoassays. RESULTS: We found elevated ECP at baseline in the total active IBD group when compared to the inactive IBD and control groups, decreasing during treatment. Serum ECP was also elevated in the active UC and CD groups when compared to the inactive UC and CD groups, and correlated with clinical UC and CD activity (R = 0.57 and R = 0.52, p < 0.05, respectively) and duration of the clinical manifestation in UC (R = 0.62, p < 0.05) but not with the disease location in the gastrointestinal tract, or endoscopic and histopathological activity. CONCLUSIONS: Evaluation of serum ECP in children with IBD may be useful in disease activity assessment at onset and during the treatment.
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spelling pubmed-42960542015-01-26 Clinical value of serum eosinophilic cationic protein assessment in children with inflammatory bowel disease Wędrychowicz, Andrzej Tomasik, Przemysław Pieczarkowski, Stanisław Kowalska-Duplaga, Kinga Grzenda-Adamek, Zofia Fyderek, Krzysztof Arch Med Sci Clinical Research INTRODUCTION: Eosinophils contribute to the pathogenesis of inflammatory bowel disease (IBD) in the intestine. Eosinophilic cationic protein (ECP) is one of the most important eosinophilic specific mediators released during activation. The aim of the study was to evaluate the clinical value of serum ECP determination in children with active and inactive IBD and its correlation with disease activity. MATERIAL AND METHODS: There were 125 children with IBD (63 with Crohn's disease – CD, 44 with ulcerative colitis – UC, 18 indeterminate colitis – IC) enrolled in the study. Among them 83 children were in the active phase of the disease, while the remaining 42 were in remission. The control group consisted of 56 healthy children. The ECP was assessed three times in children with active IBD, at baseline and after 2 and 6 weeks of treatment and once in children with inactive IBD and controls using fluoroenzymeimmunoassays. RESULTS: We found elevated ECP at baseline in the total active IBD group when compared to the inactive IBD and control groups, decreasing during treatment. Serum ECP was also elevated in the active UC and CD groups when compared to the inactive UC and CD groups, and correlated with clinical UC and CD activity (R = 0.57 and R = 0.52, p < 0.05, respectively) and duration of the clinical manifestation in UC (R = 0.62, p < 0.05) but not with the disease location in the gastrointestinal tract, or endoscopic and histopathological activity. CONCLUSIONS: Evaluation of serum ECP in children with IBD may be useful in disease activity assessment at onset and during the treatment. Termedia Publishing House 2013-04-09 2014-12-22 /pmc/articles/PMC4296054/ /pubmed/25624851 http://dx.doi.org/10.5114/aoms.2013.34415 Text en Copyright © 2014 Termedia & Banach http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an Open Access article distributed under the terms of the Creative Commons Attribution-Noncommercial 3.0 Unported License, permitting all non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research
Wędrychowicz, Andrzej
Tomasik, Przemysław
Pieczarkowski, Stanisław
Kowalska-Duplaga, Kinga
Grzenda-Adamek, Zofia
Fyderek, Krzysztof
Clinical value of serum eosinophilic cationic protein assessment in children with inflammatory bowel disease
title Clinical value of serum eosinophilic cationic protein assessment in children with inflammatory bowel disease
title_full Clinical value of serum eosinophilic cationic protein assessment in children with inflammatory bowel disease
title_fullStr Clinical value of serum eosinophilic cationic protein assessment in children with inflammatory bowel disease
title_full_unstemmed Clinical value of serum eosinophilic cationic protein assessment in children with inflammatory bowel disease
title_short Clinical value of serum eosinophilic cationic protein assessment in children with inflammatory bowel disease
title_sort clinical value of serum eosinophilic cationic protein assessment in children with inflammatory bowel disease
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4296054/
https://www.ncbi.nlm.nih.gov/pubmed/25624851
http://dx.doi.org/10.5114/aoms.2013.34415
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