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Prognostic Value of Colonic Tissue and Blood Eosinophils in Ulcerative Colitis

BACKGROUND: It has been suggested that eosinophils may be a prognostic marker of disease outcome in ulcerative colitis (UC), but conflicting data exist. The objective was to investigate the extent of mucosal eosinophils and peripheral blood eosinophil count in newly diagnosed UC patients and to inve...

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Autores principales: Haasnoot, Maria L, Mookhoek, Aart, Duijvestein, Marjolijn, D’Haens, Geert R A M, Bredenoord, Albert J
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825288/
https://www.ncbi.nlm.nih.gov/pubmed/35275200
http://dx.doi.org/10.1093/ibd/izac044
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author Haasnoot, Maria L
Mookhoek, Aart
Duijvestein, Marjolijn
D’Haens, Geert R A M
Bredenoord, Albert J
author_facet Haasnoot, Maria L
Mookhoek, Aart
Duijvestein, Marjolijn
D’Haens, Geert R A M
Bredenoord, Albert J
author_sort Haasnoot, Maria L
collection PubMed
description BACKGROUND: It has been suggested that eosinophils may be a prognostic marker of disease outcome in ulcerative colitis (UC), but conflicting data exist. The objective was to investigate the extent of mucosal eosinophils and peripheral blood eosinophil count in newly diagnosed UC patients and to investigate its predictive value in short- and long-term disease outcomes. METHODS: The degree of eosinophilia in baseline colonic biopsies and blood of newly diagnosed UC patients was retrospectively analyzed. It was investigated if tissue and blood eosinophilia could be a marker of a severe phenotype of UC, defined as the need for corticosteroids or immunomodulators in the first year or treatment with therapeutic monoclonal antibodies or colectomy during follow-up. Time to therapeutic monoclonal antibodies and time to colectomy were also evaluated as outcomes. RESULTS: There were 103 UC patients (median age 26 years) included. Median tissue peak eosinophil count (PEC) was 70.0 and median peripheral blood eosinophil count was 0.3 × 10(9)/L at diagnosis. Tissue PEC (r = -0.161, P = .104) and blood eosinophil count (r = 0.022, P = .877) were not correlated with the severity of histologic inflammation. Logistic regression analyses did not identify PEC and blood eosinophil count as predictors of more severe disease outcomes. Tissue PEC and peripheral blood eosinophil count did not predict the time the initiation of therapeutic monoclonal antibodies or colectomy. CONCLUSION: Baseline tissue or peripheral blood eosinophils are not markers of disease activity and cannot be used as a predictor of severe disease outcomes in both adults and children with UC.
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spelling pubmed-98252882023-01-09 Prognostic Value of Colonic Tissue and Blood Eosinophils in Ulcerative Colitis Haasnoot, Maria L Mookhoek, Aart Duijvestein, Marjolijn D’Haens, Geert R A M Bredenoord, Albert J Inflamm Bowel Dis Clinical Research BACKGROUND: It has been suggested that eosinophils may be a prognostic marker of disease outcome in ulcerative colitis (UC), but conflicting data exist. The objective was to investigate the extent of mucosal eosinophils and peripheral blood eosinophil count in newly diagnosed UC patients and to investigate its predictive value in short- and long-term disease outcomes. METHODS: The degree of eosinophilia in baseline colonic biopsies and blood of newly diagnosed UC patients was retrospectively analyzed. It was investigated if tissue and blood eosinophilia could be a marker of a severe phenotype of UC, defined as the need for corticosteroids or immunomodulators in the first year or treatment with therapeutic monoclonal antibodies or colectomy during follow-up. Time to therapeutic monoclonal antibodies and time to colectomy were also evaluated as outcomes. RESULTS: There were 103 UC patients (median age 26 years) included. Median tissue peak eosinophil count (PEC) was 70.0 and median peripheral blood eosinophil count was 0.3 × 10(9)/L at diagnosis. Tissue PEC (r = -0.161, P = .104) and blood eosinophil count (r = 0.022, P = .877) were not correlated with the severity of histologic inflammation. Logistic regression analyses did not identify PEC and blood eosinophil count as predictors of more severe disease outcomes. Tissue PEC and peripheral blood eosinophil count did not predict the time the initiation of therapeutic monoclonal antibodies or colectomy. CONCLUSION: Baseline tissue or peripheral blood eosinophils are not markers of disease activity and cannot be used as a predictor of severe disease outcomes in both adults and children with UC. Oxford University Press 2022-03-11 /pmc/articles/PMC9825288/ /pubmed/35275200 http://dx.doi.org/10.1093/ibd/izac044 Text en © 2022 Crohn’s & Colitis Foundation. Published by Oxford University Press on behalf of Crohn’s & Colitis Foundation. https://creativecommons.org/licenses/by-nc/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution-NonCommercial License (https://creativecommons.org/licenses/by-nc/4.0/), which permits non-commercial re-use, distribution, and reproduction in any medium, provided the original work is properly cited. For commercial re-use, please contact journals.permissions@oup.com
spellingShingle Clinical Research
Haasnoot, Maria L
Mookhoek, Aart
Duijvestein, Marjolijn
D’Haens, Geert R A M
Bredenoord, Albert J
Prognostic Value of Colonic Tissue and Blood Eosinophils in Ulcerative Colitis
title Prognostic Value of Colonic Tissue and Blood Eosinophils in Ulcerative Colitis
title_full Prognostic Value of Colonic Tissue and Blood Eosinophils in Ulcerative Colitis
title_fullStr Prognostic Value of Colonic Tissue and Blood Eosinophils in Ulcerative Colitis
title_full_unstemmed Prognostic Value of Colonic Tissue and Blood Eosinophils in Ulcerative Colitis
title_short Prognostic Value of Colonic Tissue and Blood Eosinophils in Ulcerative Colitis
title_sort prognostic value of colonic tissue and blood eosinophils in ulcerative colitis
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9825288/
https://www.ncbi.nlm.nih.gov/pubmed/35275200
http://dx.doi.org/10.1093/ibd/izac044
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