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Relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease

In adult inflammatory bowel disease (IBD) patients, there is a strong discrepancy between symptoms and biomarkers of inflammation. Data on pediatric IBD patients are conflicting. Therefore, we aimed to investigate the relationship between clinical symptoms and biomarkers of inflammation in pediatric...

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Autores principales: Hoekman, Daniël R., Diederen, Kay, Koot, Bart G. P., Tabbers, Merit M., Kindermann, Angelika, Benninga, Marc A.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031739/
https://www.ncbi.nlm.nih.gov/pubmed/27573259
http://dx.doi.org/10.1007/s00431-016-2762-2
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author Hoekman, Daniël R.
Diederen, Kay
Koot, Bart G. P.
Tabbers, Merit M.
Kindermann, Angelika
Benninga, Marc A.
author_facet Hoekman, Daniël R.
Diederen, Kay
Koot, Bart G. P.
Tabbers, Merit M.
Kindermann, Angelika
Benninga, Marc A.
author_sort Hoekman, Daniël R.
collection PubMed
description In adult inflammatory bowel disease (IBD) patients, there is a strong discrepancy between symptoms and biomarkers of inflammation. Data on pediatric IBD patients are conflicting. Therefore, we aimed to investigate the relationship between clinical symptoms and biomarkers of inflammation in pediatric IBD. Patients aged <18 years with previously diagnosed Crohn’s disease (CD) or ulcerative colitis (UC) were included. Clinical disease activity was determined using the abbreviated Pediatric CD Activity Index (aPCDAI) or Pediatric UC Activity Index (PUCAI). Biochemical disease activity was assessed using fecal calprotectin (FC) and C-reactive protein (CRP). In total, 127 patients (62 male; median age 14.9 years) were included (82 CD, 45 UC). FC correlated weakly with total aPCDAI score (r(s) = 0.32; 95 % CI 0.12–0.51; p = 0.003) and total PUCAI score (r(s) = 0.36; 95 % CI 0.07–0.62; p = 0.015). Only aPCDAI components abdominal examination and perirectal disease and PUCAI component activity level had a significant correlation with levels of FC. CRP correlated weakly with total aPCDAI score (r(s) = 0.28; 95 % CI 0.05–0.46; p = 0.012) and aPCDAI components abdominal examination and activity level. No significant correlation was observed between CRP and total PUCAI score (r(s) = 0.01; 95 % CI −0.34–0.29; p = 0.961) or individual PUCAI components. Conclusion: There is a strong discrepancy between clinical symptoms and biomarkers of inflammation in children with IBD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00431-016-2762-2) contains supplementary material, which is available to authorized users.
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spelling pubmed-50317392016-10-09 Relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease Hoekman, Daniël R. Diederen, Kay Koot, Bart G. P. Tabbers, Merit M. Kindermann, Angelika Benninga, Marc A. Eur J Pediatr Original Article In adult inflammatory bowel disease (IBD) patients, there is a strong discrepancy between symptoms and biomarkers of inflammation. Data on pediatric IBD patients are conflicting. Therefore, we aimed to investigate the relationship between clinical symptoms and biomarkers of inflammation in pediatric IBD. Patients aged <18 years with previously diagnosed Crohn’s disease (CD) or ulcerative colitis (UC) were included. Clinical disease activity was determined using the abbreviated Pediatric CD Activity Index (aPCDAI) or Pediatric UC Activity Index (PUCAI). Biochemical disease activity was assessed using fecal calprotectin (FC) and C-reactive protein (CRP). In total, 127 patients (62 male; median age 14.9 years) were included (82 CD, 45 UC). FC correlated weakly with total aPCDAI score (r(s) = 0.32; 95 % CI 0.12–0.51; p = 0.003) and total PUCAI score (r(s) = 0.36; 95 % CI 0.07–0.62; p = 0.015). Only aPCDAI components abdominal examination and perirectal disease and PUCAI component activity level had a significant correlation with levels of FC. CRP correlated weakly with total aPCDAI score (r(s) = 0.28; 95 % CI 0.05–0.46; p = 0.012) and aPCDAI components abdominal examination and activity level. No significant correlation was observed between CRP and total PUCAI score (r(s) = 0.01; 95 % CI −0.34–0.29; p = 0.961) or individual PUCAI components. Conclusion: There is a strong discrepancy between clinical symptoms and biomarkers of inflammation in children with IBD. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00431-016-2762-2) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-08-29 2016 /pmc/articles/PMC5031739/ /pubmed/27573259 http://dx.doi.org/10.1007/s00431-016-2762-2 Text en © The Author(s) 2016 Open Access This article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made.
spellingShingle Original Article
Hoekman, Daniël R.
Diederen, Kay
Koot, Bart G. P.
Tabbers, Merit M.
Kindermann, Angelika
Benninga, Marc A.
Relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease
title Relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease
title_full Relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease
title_fullStr Relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease
title_full_unstemmed Relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease
title_short Relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease
title_sort relationship of clinical symptoms with biomarkers of inflammation in pediatric inflammatory bowel disease
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5031739/
https://www.ncbi.nlm.nih.gov/pubmed/27573259
http://dx.doi.org/10.1007/s00431-016-2762-2
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