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Identifying the etiology and pathophysiology underlying stunting and environmental enteropathy: study protocol of the AFRIBIOTA project

BACKGROUND: Globally one out of four children under 5 years is affected by linear growth delay (stunting). This syndrome has severe long-term sequelae including increased risk of illness and mortality and delayed psychomotor development. Stunting is a syndrome that is linked to poor nutrition and re...

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Autores principales: Vonaesch, Pascale, Randremanana, Rindra, Gody, Jean-Chrysostome, Collard, Jean-Marc, Giles-Vernick, Tamara, Doria, Maria, Vigan-Womas, Inès, Rubbo, Pierre-Alain, Etienne, Aurélie, Andriatahirintsoa, Emilson Jean, Kapel, Nathalie, Brown, Eric, Huus, Kelsey E., Duffy, Darragh, Finlay, B.Brett, Hasan, Milena, Hunald, Francis Allen, Robinson, Annick, Manirakiza, Alexandre, Wegener-Parfrey, Laura, Vray, Muriel, Sansonetti, Philippe J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2018
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053792/
https://www.ncbi.nlm.nih.gov/pubmed/30025542
http://dx.doi.org/10.1186/s12887-018-1189-5
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author Vonaesch, Pascale
Randremanana, Rindra
Gody, Jean-Chrysostome
Collard, Jean-Marc
Giles-Vernick, Tamara
Doria, Maria
Vigan-Womas, Inès
Rubbo, Pierre-Alain
Etienne, Aurélie
Andriatahirintsoa, Emilson Jean
Kapel, Nathalie
Brown, Eric
Huus, Kelsey E.
Duffy, Darragh
Finlay, B.Brett
Hasan, Milena
Hunald, Francis Allen
Robinson, Annick
Manirakiza, Alexandre
Wegener-Parfrey, Laura
Vray, Muriel
Sansonetti, Philippe J.
author_facet Vonaesch, Pascale
Randremanana, Rindra
Gody, Jean-Chrysostome
Collard, Jean-Marc
Giles-Vernick, Tamara
Doria, Maria
Vigan-Womas, Inès
Rubbo, Pierre-Alain
Etienne, Aurélie
Andriatahirintsoa, Emilson Jean
Kapel, Nathalie
Brown, Eric
Huus, Kelsey E.
Duffy, Darragh
Finlay, B.Brett
Hasan, Milena
Hunald, Francis Allen
Robinson, Annick
Manirakiza, Alexandre
Wegener-Parfrey, Laura
Vray, Muriel
Sansonetti, Philippe J.
author_sort Vonaesch, Pascale
collection PubMed
description BACKGROUND: Globally one out of four children under 5 years is affected by linear growth delay (stunting). This syndrome has severe long-term sequelae including increased risk of illness and mortality and delayed psychomotor development. Stunting is a syndrome that is linked to poor nutrition and repeated infections. To date, the treatment of stunted children is challenging as the underlying etiology and pathophysiological mechanisms remain elusive. We hypothesize that pediatric environmental enteropathy (PEE), a chronic inflammation of the small intestine, plays a major role in the pathophysiology of stunting, failure of nutritional interventions and diminished response to oral vaccines, potentially via changes in the composition of the pro- and eukaryotic intestinal communities. The main objective of AFRIBIOTA is to describe the intestinal dysbiosis observed in the context of stunting and to link it to PEE. Secondary objectives include the identification of the broader socio-economic environment and biological and environmental risk factors for stunting and PEE as well as the testing of a set of easy-to-use candidate biomarkers for PEE. We also assess host outcomes including mucosal and systemic immunity and psychomotor development. This article describes the rationale and study protocol of the AFRIBIOTA project. METHODS: AFRIBIOTA is a case-control study for stunting recruiting children in Bangui, Central African Republic and in Antananarivo, Madagascar. In each country, 460 children aged 2–5 years with no overt signs of gastrointestinal disease are recruited (260 with no growth delay, 100 moderately stunted and 100 severely stunted). We compare the intestinal microbiota composition (gastric and small intestinal aspirates; feces), the mucosal and systemic immune status and the psychomotor development of children with stunting and/or PEE compared to non-stunted controls. We also perform anthropological and epidemiological investigations of the children’s broader living conditions and assess risk factors using a standardized questionnaire. DISCUSSION: To date, the pathophysiology and risk factors of stunting and PEE have been insufficiently investigated. AFRIBIOTA will add new insights into the pathophysiology underlying stunting and PEE and in doing so will enable implementation of new biomarkers and design of evidence-based treatment strategies for these two syndromes.
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spelling pubmed-60537922018-07-23 Identifying the etiology and pathophysiology underlying stunting and environmental enteropathy: study protocol of the AFRIBIOTA project Vonaesch, Pascale Randremanana, Rindra Gody, Jean-Chrysostome Collard, Jean-Marc Giles-Vernick, Tamara Doria, Maria Vigan-Womas, Inès Rubbo, Pierre-Alain Etienne, Aurélie Andriatahirintsoa, Emilson Jean Kapel, Nathalie Brown, Eric Huus, Kelsey E. Duffy, Darragh Finlay, B.Brett Hasan, Milena Hunald, Francis Allen Robinson, Annick Manirakiza, Alexandre Wegener-Parfrey, Laura Vray, Muriel Sansonetti, Philippe J. BMC Pediatr Study Protocol BACKGROUND: Globally one out of four children under 5 years is affected by linear growth delay (stunting). This syndrome has severe long-term sequelae including increased risk of illness and mortality and delayed psychomotor development. Stunting is a syndrome that is linked to poor nutrition and repeated infections. To date, the treatment of stunted children is challenging as the underlying etiology and pathophysiological mechanisms remain elusive. We hypothesize that pediatric environmental enteropathy (PEE), a chronic inflammation of the small intestine, plays a major role in the pathophysiology of stunting, failure of nutritional interventions and diminished response to oral vaccines, potentially via changes in the composition of the pro- and eukaryotic intestinal communities. The main objective of AFRIBIOTA is to describe the intestinal dysbiosis observed in the context of stunting and to link it to PEE. Secondary objectives include the identification of the broader socio-economic environment and biological and environmental risk factors for stunting and PEE as well as the testing of a set of easy-to-use candidate biomarkers for PEE. We also assess host outcomes including mucosal and systemic immunity and psychomotor development. This article describes the rationale and study protocol of the AFRIBIOTA project. METHODS: AFRIBIOTA is a case-control study for stunting recruiting children in Bangui, Central African Republic and in Antananarivo, Madagascar. In each country, 460 children aged 2–5 years with no overt signs of gastrointestinal disease are recruited (260 with no growth delay, 100 moderately stunted and 100 severely stunted). We compare the intestinal microbiota composition (gastric and small intestinal aspirates; feces), the mucosal and systemic immune status and the psychomotor development of children with stunting and/or PEE compared to non-stunted controls. We also perform anthropological and epidemiological investigations of the children’s broader living conditions and assess risk factors using a standardized questionnaire. DISCUSSION: To date, the pathophysiology and risk factors of stunting and PEE have been insufficiently investigated. AFRIBIOTA will add new insights into the pathophysiology underlying stunting and PEE and in doing so will enable implementation of new biomarkers and design of evidence-based treatment strategies for these two syndromes. BioMed Central 2018-07-19 /pmc/articles/PMC6053792/ /pubmed/30025542 http://dx.doi.org/10.1186/s12887-018-1189-5 Text en © The Author(s). 2018 Open AccessThis 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. 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 Study Protocol
Vonaesch, Pascale
Randremanana, Rindra
Gody, Jean-Chrysostome
Collard, Jean-Marc
Giles-Vernick, Tamara
Doria, Maria
Vigan-Womas, Inès
Rubbo, Pierre-Alain
Etienne, Aurélie
Andriatahirintsoa, Emilson Jean
Kapel, Nathalie
Brown, Eric
Huus, Kelsey E.
Duffy, Darragh
Finlay, B.Brett
Hasan, Milena
Hunald, Francis Allen
Robinson, Annick
Manirakiza, Alexandre
Wegener-Parfrey, Laura
Vray, Muriel
Sansonetti, Philippe J.
Identifying the etiology and pathophysiology underlying stunting and environmental enteropathy: study protocol of the AFRIBIOTA project
title Identifying the etiology and pathophysiology underlying stunting and environmental enteropathy: study protocol of the AFRIBIOTA project
title_full Identifying the etiology and pathophysiology underlying stunting and environmental enteropathy: study protocol of the AFRIBIOTA project
title_fullStr Identifying the etiology and pathophysiology underlying stunting and environmental enteropathy: study protocol of the AFRIBIOTA project
title_full_unstemmed Identifying the etiology and pathophysiology underlying stunting and environmental enteropathy: study protocol of the AFRIBIOTA project
title_short Identifying the etiology and pathophysiology underlying stunting and environmental enteropathy: study protocol of the AFRIBIOTA project
title_sort identifying the etiology and pathophysiology underlying stunting and environmental enteropathy: study protocol of the afribiota project
topic Study Protocol
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6053792/
https://www.ncbi.nlm.nih.gov/pubmed/30025542
http://dx.doi.org/10.1186/s12887-018-1189-5
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