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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...

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Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2014
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.
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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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