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Functional Gastrointestinal Disorders Induced by Esophageal Atresia Surgery: Is It Valid in Humans?

BACKGROUND/AIMS: Functional gastrointestinal disorders (FGID) affect 15%-20% of the general pediatric and adult population. Animal models suggest that a neonatal stress such as invasive procedures and maternal separation could be responsible for visceral hypersensitivity and FGID. We tested the hypo...

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Autores principales: Halac, Ugur, Revillion, Marine, Michaud, Laurent, Gottrand, Frédéric, Faure, Christophe
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Korean Society of Neurogastroenterology and Motility 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3479254/
https://www.ncbi.nlm.nih.gov/pubmed/23106001
http://dx.doi.org/10.5056/jnm.2012.18.4.406
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author Halac, Ugur
Revillion, Marine
Michaud, Laurent
Gottrand, Frédéric
Faure, Christophe
author_facet Halac, Ugur
Revillion, Marine
Michaud, Laurent
Gottrand, Frédéric
Faure, Christophe
author_sort Halac, Ugur
collection PubMed
description BACKGROUND/AIMS: Functional gastrointestinal disorders (FGID) affect 15%-20% of the general pediatric and adult population. Animal models suggest that a neonatal stress such as invasive procedures and maternal separation could be responsible for visceral hypersensitivity and FGID. We tested the hypothesis that congenital esophageal atresia (EA), a condition corrected during the neonatal period and associated with multiple stresses, is a clinically significant risk factor for the development of FGID later in life. We postulated that, to be clinically significant, the effect of neonatal stress on the incidence of FGID should be as strong as that of enteric infections in the development of irritable bowel syndrome in children. METHODS: Subjects with EA and healthy controls were enrolled in this multicenter cohort study. Gastrointestinal symptoms were assessed by a questionnaire and FGID was diagnosed using the Rome III criteria. RESULTS: Fifty-three children (25 girls; median age, 12 years) with EA were compared to 72 age- and sex-matched controls. Although 11 children with EA (21%) had a FGID diagnosis versus 8 controls (11%), this difference was not significant (χ(2) = 2.20, P > 0.05). In subjects with EA, the presence of associated malformations, the occurrence of complications during the first month, and the length of hospital stay > 30 days did not influence the incidence of FGID. Chronic abdominal pain was present in 38% of subjects with EA versus 25% of controls (P > 0.05). CONCLUSIONS: Neonatal stress secondary to surgical correction of EA is not a clinically significant risk factor for the development of FGID in childhood.
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spelling pubmed-34792542012-10-26 Functional Gastrointestinal Disorders Induced by Esophageal Atresia Surgery: Is It Valid in Humans? Halac, Ugur Revillion, Marine Michaud, Laurent Gottrand, Frédéric Faure, Christophe J Neurogastroenterol Motil Original Article BACKGROUND/AIMS: Functional gastrointestinal disorders (FGID) affect 15%-20% of the general pediatric and adult population. Animal models suggest that a neonatal stress such as invasive procedures and maternal separation could be responsible for visceral hypersensitivity and FGID. We tested the hypothesis that congenital esophageal atresia (EA), a condition corrected during the neonatal period and associated with multiple stresses, is a clinically significant risk factor for the development of FGID later in life. We postulated that, to be clinically significant, the effect of neonatal stress on the incidence of FGID should be as strong as that of enteric infections in the development of irritable bowel syndrome in children. METHODS: Subjects with EA and healthy controls were enrolled in this multicenter cohort study. Gastrointestinal symptoms were assessed by a questionnaire and FGID was diagnosed using the Rome III criteria. RESULTS: Fifty-three children (25 girls; median age, 12 years) with EA were compared to 72 age- and sex-matched controls. Although 11 children with EA (21%) had a FGID diagnosis versus 8 controls (11%), this difference was not significant (χ(2) = 2.20, P > 0.05). In subjects with EA, the presence of associated malformations, the occurrence of complications during the first month, and the length of hospital stay > 30 days did not influence the incidence of FGID. Chronic abdominal pain was present in 38% of subjects with EA versus 25% of controls (P > 0.05). CONCLUSIONS: Neonatal stress secondary to surgical correction of EA is not a clinically significant risk factor for the development of FGID in childhood. Korean Society of Neurogastroenterology and Motility 2012-10 2012-10-09 /pmc/articles/PMC3479254/ /pubmed/23106001 http://dx.doi.org/10.5056/jnm.2012.18.4.406 Text en © 2012 The Korean Society of Neurogastroenterology and Motility http://creativecommons.org/licenses/by-nc/3.0 This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Article
Halac, Ugur
Revillion, Marine
Michaud, Laurent
Gottrand, Frédéric
Faure, Christophe
Functional Gastrointestinal Disorders Induced by Esophageal Atresia Surgery: Is It Valid in Humans?
title Functional Gastrointestinal Disorders Induced by Esophageal Atresia Surgery: Is It Valid in Humans?
title_full Functional Gastrointestinal Disorders Induced by Esophageal Atresia Surgery: Is It Valid in Humans?
title_fullStr Functional Gastrointestinal Disorders Induced by Esophageal Atresia Surgery: Is It Valid in Humans?
title_full_unstemmed Functional Gastrointestinal Disorders Induced by Esophageal Atresia Surgery: Is It Valid in Humans?
title_short Functional Gastrointestinal Disorders Induced by Esophageal Atresia Surgery: Is It Valid in Humans?
title_sort functional gastrointestinal disorders induced by esophageal atresia surgery: is it valid in humans?
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3479254/
https://www.ncbi.nlm.nih.gov/pubmed/23106001
http://dx.doi.org/10.5056/jnm.2012.18.4.406
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