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Fecal calprotectin: a marker for clinical differentiation of microscopic colitis and irritable bowel syndrome

BACKGROUND: The aim of this study is to compare two methods for measuring fecal calprotectin (FC) concentration and to evaluate the possibility of differentiation between microscopic colitis (MC) and irritable bowel syndrome (IBS). METHODS: Twenty-three patients with MC (six patients with active dis...

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Autores principales: von Arnim, Ulrike, Wex, Thomas, Ganzert, Christine, Schulz, Christian, Malfertheiner, Peter
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Dove Medical Press 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849404/
https://www.ncbi.nlm.nih.gov/pubmed/27147826
http://dx.doi.org/10.2147/CEG.S97701
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author von Arnim, Ulrike
Wex, Thomas
Ganzert, Christine
Schulz, Christian
Malfertheiner, Peter
author_facet von Arnim, Ulrike
Wex, Thomas
Ganzert, Christine
Schulz, Christian
Malfertheiner, Peter
author_sort von Arnim, Ulrike
collection PubMed
description BACKGROUND: The aim of this study is to compare two methods for measuring fecal calprotectin (FC) concentration and to evaluate the possibility of differentiation between microscopic colitis (MC) and irritable bowel syndrome (IBS). METHODS: Twenty-three patients with MC (six patients with active disease and 17 patients retested in remission) and 20 patients with IBS were prospectively included in this study. Active disease state of MC was determined by clinical symptoms of >3 bowel movements per day and histological correlate. All patients underwent ileocolonoscopy, including segmental biopsy samples for histology. FC levels in stool samples were analyzed using a rapid test system (Quantum Blue(®)) and an enzyme-linked immunosorbent assay (ELISA). RESULTS: FC levels were significantly higher in patients with active MC (median 48 μg/g [23–106]) compared to patients with IBS (median 2 μg/g [1–111.83]), P=0.0001 using an ELISA. FC level of patients with MC in remission was 22 μg/g (1–106.4), which is similar to those identified in patients with IBS. The difference of FC levels between active MC and IBS was not detected by the FC rapid test (P=0.635). DISCUSSION: FC levels might serve as parameter for differentiation between patients with active MC and IBS. Since there is no surrogate marker available at present for MC, FC appears to be a candidate for differentiating MC from IBS. CONCLUSION: High FC levels, which were analyzed by ELISA, are a potential marker for patients with active MC compared to those with IBS. The FC rapid test was less suitable for this purpose.
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spelling pubmed-48494042016-05-04 Fecal calprotectin: a marker for clinical differentiation of microscopic colitis and irritable bowel syndrome von Arnim, Ulrike Wex, Thomas Ganzert, Christine Schulz, Christian Malfertheiner, Peter Clin Exp Gastroenterol Clinical Trial Report BACKGROUND: The aim of this study is to compare two methods for measuring fecal calprotectin (FC) concentration and to evaluate the possibility of differentiation between microscopic colitis (MC) and irritable bowel syndrome (IBS). METHODS: Twenty-three patients with MC (six patients with active disease and 17 patients retested in remission) and 20 patients with IBS were prospectively included in this study. Active disease state of MC was determined by clinical symptoms of >3 bowel movements per day and histological correlate. All patients underwent ileocolonoscopy, including segmental biopsy samples for histology. FC levels in stool samples were analyzed using a rapid test system (Quantum Blue(®)) and an enzyme-linked immunosorbent assay (ELISA). RESULTS: FC levels were significantly higher in patients with active MC (median 48 μg/g [23–106]) compared to patients with IBS (median 2 μg/g [1–111.83]), P=0.0001 using an ELISA. FC level of patients with MC in remission was 22 μg/g (1–106.4), which is similar to those identified in patients with IBS. The difference of FC levels between active MC and IBS was not detected by the FC rapid test (P=0.635). DISCUSSION: FC levels might serve as parameter for differentiation between patients with active MC and IBS. Since there is no surrogate marker available at present for MC, FC appears to be a candidate for differentiating MC from IBS. CONCLUSION: High FC levels, which were analyzed by ELISA, are a potential marker for patients with active MC compared to those with IBS. The FC rapid test was less suitable for this purpose. Dove Medical Press 2016-04-21 /pmc/articles/PMC4849404/ /pubmed/27147826 http://dx.doi.org/10.2147/CEG.S97701 Text en © 2016 von Arnim et al. This work is published and licensed by Dove Medical Press Limited The full terms of this license are available at https://www.dovepress.com/terms.php and incorporate the Creative Commons Attribution – Non Commercial (unported, v3.0) License (http://creativecommons.org/licenses/by-nc/3.0/). By accessing the work you hereby accept the Terms. Non-commercial uses of the work are permitted without any further permission from Dove Medical Press Limited, provided the work is properly attributed.
spellingShingle Clinical Trial Report
von Arnim, Ulrike
Wex, Thomas
Ganzert, Christine
Schulz, Christian
Malfertheiner, Peter
Fecal calprotectin: a marker for clinical differentiation of microscopic colitis and irritable bowel syndrome
title Fecal calprotectin: a marker for clinical differentiation of microscopic colitis and irritable bowel syndrome
title_full Fecal calprotectin: a marker for clinical differentiation of microscopic colitis and irritable bowel syndrome
title_fullStr Fecal calprotectin: a marker for clinical differentiation of microscopic colitis and irritable bowel syndrome
title_full_unstemmed Fecal calprotectin: a marker for clinical differentiation of microscopic colitis and irritable bowel syndrome
title_short Fecal calprotectin: a marker for clinical differentiation of microscopic colitis and irritable bowel syndrome
title_sort fecal calprotectin: a marker for clinical differentiation of microscopic colitis and irritable bowel syndrome
topic Clinical Trial Report
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4849404/
https://www.ncbi.nlm.nih.gov/pubmed/27147826
http://dx.doi.org/10.2147/CEG.S97701
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