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Mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction: a pilot randomized controlled trial
BACKGROUND: Environmental enteric dysfunction (EED) is an acquired syndrome of impaired gastrointestinal mucosal barrier function that is thought to play a key role in the pathogenesis of stunting in early life. It has been conceptualized as an adaptive response to excess environmental pathogen expo...
Autores principales: | , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2014
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243388/ https://www.ncbi.nlm.nih.gov/pubmed/25189855 http://dx.doi.org/10.1186/s12916-014-0133-2 |
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author | Jones, Kelsey DJ Hünten-Kirsch, Barbara Laving, Ahmed MR Munyi, Caroline W Ngari, Moses Mikusa, Jenifer Mulongo, Musa M Odera, Dennis Nassir, H Samira Timbwa, Molline Owino, Moses Fegan, Greg Murch, Simon H Sullivan, Peter B Warner, John O Berkley, James A |
author_facet | Jones, Kelsey DJ Hünten-Kirsch, Barbara Laving, Ahmed MR Munyi, Caroline W Ngari, Moses Mikusa, Jenifer Mulongo, Musa M Odera, Dennis Nassir, H Samira Timbwa, Molline Owino, Moses Fegan, Greg Murch, Simon H Sullivan, Peter B Warner, John O Berkley, James A |
author_sort | Jones, Kelsey DJ |
collection | PubMed |
description | BACKGROUND: Environmental enteric dysfunction (EED) is an acquired syndrome of impaired gastrointestinal mucosal barrier function that is thought to play a key role in the pathogenesis of stunting in early life. It has been conceptualized as an adaptive response to excess environmental pathogen exposure. However, it is clinically similar to other inflammatory enteropathies, which result from both host and environmental triggers, and for which immunomodulation is a cornerstone of therapy. METHODS: In this pilot double-blind randomized placebo-controlled trial, 44 children with severe acute malnutrition and evidence of EED were assigned to treatment with mesalazine or placebo for 28 days during nutritional rehabilitation. Primary outcomes were safety and acceptability of the intervention. RESULTS: Treatment with mesalazine was safe: there was no excess of adverse events, evidence of deterioration in intestinal barrier integrity or impact on nutritional recovery. There were modest reductions in several inflammatory markers with mesalazine compared to placebo. Depression of the growth hormone – insulin-like growth factor-1 axis was evident at enrollment and associated with inflammatory activation. Increases in the former and decreases in the latter correlated with linear growth. CONCLUSIONS: Intestinal inflammation in EED is non-essential for mucosal homeostasis and is at least partly maladaptive. Further trials of gut-specific immunomodulatory therapies targeting host inflammatory activation in order to optimize the growth benefits of nutritional rehabilitation and to address stunting are warranted. Funded by The Wellcome Trust. TRIAL REGISTRATION: Registered at Clinicaltrials.gov NCT01841099. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-014-0133-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-4243388 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2014 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-42433882014-11-26 Mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction: a pilot randomized controlled trial Jones, Kelsey DJ Hünten-Kirsch, Barbara Laving, Ahmed MR Munyi, Caroline W Ngari, Moses Mikusa, Jenifer Mulongo, Musa M Odera, Dennis Nassir, H Samira Timbwa, Molline Owino, Moses Fegan, Greg Murch, Simon H Sullivan, Peter B Warner, John O Berkley, James A BMC Med Research Article BACKGROUND: Environmental enteric dysfunction (EED) is an acquired syndrome of impaired gastrointestinal mucosal barrier function that is thought to play a key role in the pathogenesis of stunting in early life. It has been conceptualized as an adaptive response to excess environmental pathogen exposure. However, it is clinically similar to other inflammatory enteropathies, which result from both host and environmental triggers, and for which immunomodulation is a cornerstone of therapy. METHODS: In this pilot double-blind randomized placebo-controlled trial, 44 children with severe acute malnutrition and evidence of EED were assigned to treatment with mesalazine or placebo for 28 days during nutritional rehabilitation. Primary outcomes were safety and acceptability of the intervention. RESULTS: Treatment with mesalazine was safe: there was no excess of adverse events, evidence of deterioration in intestinal barrier integrity or impact on nutritional recovery. There were modest reductions in several inflammatory markers with mesalazine compared to placebo. Depression of the growth hormone – insulin-like growth factor-1 axis was evident at enrollment and associated with inflammatory activation. Increases in the former and decreases in the latter correlated with linear growth. CONCLUSIONS: Intestinal inflammation in EED is non-essential for mucosal homeostasis and is at least partly maladaptive. Further trials of gut-specific immunomodulatory therapies targeting host inflammatory activation in order to optimize the growth benefits of nutritional rehabilitation and to address stunting are warranted. Funded by The Wellcome Trust. TRIAL REGISTRATION: Registered at Clinicaltrials.gov NCT01841099. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s12916-014-0133-2) contains supplementary material, which is available to authorized users. BioMed Central 2014-08-14 /pmc/articles/PMC4243388/ /pubmed/25189855 http://dx.doi.org/10.1186/s12916-014-0133-2 Text en © Jones et al.; licensee BioMed Central 2014 This is an Open Access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/4.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly credited. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Jones, Kelsey DJ Hünten-Kirsch, Barbara Laving, Ahmed MR Munyi, Caroline W Ngari, Moses Mikusa, Jenifer Mulongo, Musa M Odera, Dennis Nassir, H Samira Timbwa, Molline Owino, Moses Fegan, Greg Murch, Simon H Sullivan, Peter B Warner, John O Berkley, James A Mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction: a pilot randomized controlled trial |
title | Mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction: a pilot randomized controlled trial |
title_full | Mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction: a pilot randomized controlled trial |
title_fullStr | Mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction: a pilot randomized controlled trial |
title_full_unstemmed | Mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction: a pilot randomized controlled trial |
title_short | Mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction: a pilot randomized controlled trial |
title_sort | mesalazine in the initial management of severely acutely malnourished children with environmental enteric dysfunction: a pilot randomized controlled trial |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4243388/ https://www.ncbi.nlm.nih.gov/pubmed/25189855 http://dx.doi.org/10.1186/s12916-014-0133-2 |
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