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The association of mast cells and serotonin in children with chronic abdominal pain of unknown etiology

BACKGROUND: Abdominal pain of unknown origin affects up to 20% of school-aged children. Evaluation of children is symptom-based without clear guidelines to investigate molecular mechanisms of abdominal pain. Aberrant molecular mechanisms may increase intestinal permeability leading to interactions b...

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Autores principales: Taylor, Tara J, Youssef, Nader N, Shankar, Ravi, Kleiner, David E, Henderson, Wendy A
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974734/
https://www.ncbi.nlm.nih.gov/pubmed/20964845
http://dx.doi.org/10.1186/1756-0500-3-265
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author Taylor, Tara J
Youssef, Nader N
Shankar, Ravi
Kleiner, David E
Henderson, Wendy A
author_facet Taylor, Tara J
Youssef, Nader N
Shankar, Ravi
Kleiner, David E
Henderson, Wendy A
author_sort Taylor, Tara J
collection PubMed
description BACKGROUND: Abdominal pain of unknown origin affects up to 20% of school-aged children. Evaluation of children is symptom-based without clear guidelines to investigate molecular mechanisms of abdominal pain. Aberrant molecular mechanisms may increase intestinal permeability leading to interactions between the immune and nervous systems, subclinical inflammation, and visceral pain. This study evaluated the association between interleukin-6 (IL-6), mast cell infiltrates, and serotonin (5-HT) levels in gastrointestinal (GI) biopsies, with perceived abdominal pain in a pediatric cohort. METHODS: Clinical data and biopsy samples from pediatric patients (n = 48) with chronic abdominal pain, with and without inflammation were included. Formalin-fixed paraffin-embedded GI biopsies were sectioned and immunohistochemistry performed for IL-6 and 5-HT; mast cells were identified with toluidine blue stain. Histological findings were compared to self-reported abdominal pain between groups. RESULTS: There was significantly greater IL-6 immunoreactivity in biopsies with confirmed histologic inflammation (p = 0.004). There was a greater number of mast cells per HPF in non-inflammatory biopsies (3.5 ± 2.9) compared to the inflammatory biopsies (2.6 ± 1.8) p = 0.049. The non-inflammatory biopsy group was significantly less likely to respond to standard treatment as evidenced by higher pain reports (p = .018). Mast cells (p = .022) and 5-HT (p = .02) were significantly related to abdominal pain scores. CONCLUSIONS: A potential association between self-reported abdominal pain, number of mast cells, and 5-HT levels, which may contribute to perceived GI pain in pediatric patients may exist.
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spelling pubmed-29747342010-11-06 The association of mast cells and serotonin in children with chronic abdominal pain of unknown etiology Taylor, Tara J Youssef, Nader N Shankar, Ravi Kleiner, David E Henderson, Wendy A BMC Res Notes Research Article BACKGROUND: Abdominal pain of unknown origin affects up to 20% of school-aged children. Evaluation of children is symptom-based without clear guidelines to investigate molecular mechanisms of abdominal pain. Aberrant molecular mechanisms may increase intestinal permeability leading to interactions between the immune and nervous systems, subclinical inflammation, and visceral pain. This study evaluated the association between interleukin-6 (IL-6), mast cell infiltrates, and serotonin (5-HT) levels in gastrointestinal (GI) biopsies, with perceived abdominal pain in a pediatric cohort. METHODS: Clinical data and biopsy samples from pediatric patients (n = 48) with chronic abdominal pain, with and without inflammation were included. Formalin-fixed paraffin-embedded GI biopsies were sectioned and immunohistochemistry performed for IL-6 and 5-HT; mast cells were identified with toluidine blue stain. Histological findings were compared to self-reported abdominal pain between groups. RESULTS: There was significantly greater IL-6 immunoreactivity in biopsies with confirmed histologic inflammation (p = 0.004). There was a greater number of mast cells per HPF in non-inflammatory biopsies (3.5 ± 2.9) compared to the inflammatory biopsies (2.6 ± 1.8) p = 0.049. The non-inflammatory biopsy group was significantly less likely to respond to standard treatment as evidenced by higher pain reports (p = .018). Mast cells (p = .022) and 5-HT (p = .02) were significantly related to abdominal pain scores. CONCLUSIONS: A potential association between self-reported abdominal pain, number of mast cells, and 5-HT levels, which may contribute to perceived GI pain in pediatric patients may exist. BioMed Central 2010-10-21 /pmc/articles/PMC2974734/ /pubmed/20964845 http://dx.doi.org/10.1186/1756-0500-3-265 Text en Copyright ©2010 Henderson et al; licensee BioMed Central Ltd. http://creativecommons.org/licenses/by/2.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/2.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Taylor, Tara J
Youssef, Nader N
Shankar, Ravi
Kleiner, David E
Henderson, Wendy A
The association of mast cells and serotonin in children with chronic abdominal pain of unknown etiology
title The association of mast cells and serotonin in children with chronic abdominal pain of unknown etiology
title_full The association of mast cells and serotonin in children with chronic abdominal pain of unknown etiology
title_fullStr The association of mast cells and serotonin in children with chronic abdominal pain of unknown etiology
title_full_unstemmed The association of mast cells and serotonin in children with chronic abdominal pain of unknown etiology
title_short The association of mast cells and serotonin in children with chronic abdominal pain of unknown etiology
title_sort association of mast cells and serotonin in children with chronic abdominal pain of unknown etiology
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2974734/
https://www.ncbi.nlm.nih.gov/pubmed/20964845
http://dx.doi.org/10.1186/1756-0500-3-265
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