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Associations between Gut Microbiota and Intestinal Inflammation, Permeability and Damage in Young Malawian Children

BACKGROUND: Environmental enteric dysfunction (EED) is common in low- and middle-income countries and associated with childhood undernutrition. The composition of gut microbiota has been implicated in the pathogenesis of EED. Our aim was to assess the associations between gut microbiota and EED biom...

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Autores principales: Kortekangas, Emma, Fan, Yue-Mei, Chaima, David, Lehto, Kirsi-Maarit, Malamba-Banda, Chikondi, Matchado, Andrew, Chingwanda, Chilungamo, Liu, Zhifei, Ashorn, Ulla, Cheung, Yin Bun, Dewey, Kathryn G, Maleta, Kenneth, Ashorn, Per
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846364/
https://www.ncbi.nlm.nih.gov/pubmed/35149871
http://dx.doi.org/10.1093/tropej/fmac012
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author Kortekangas, Emma
Fan, Yue-Mei
Chaima, David
Lehto, Kirsi-Maarit
Malamba-Banda, Chikondi
Matchado, Andrew
Chingwanda, Chilungamo
Liu, Zhifei
Ashorn, Ulla
Cheung, Yin Bun
Dewey, Kathryn G
Maleta, Kenneth
Ashorn, Per
author_facet Kortekangas, Emma
Fan, Yue-Mei
Chaima, David
Lehto, Kirsi-Maarit
Malamba-Banda, Chikondi
Matchado, Andrew
Chingwanda, Chilungamo
Liu, Zhifei
Ashorn, Ulla
Cheung, Yin Bun
Dewey, Kathryn G
Maleta, Kenneth
Ashorn, Per
author_sort Kortekangas, Emma
collection PubMed
description BACKGROUND: Environmental enteric dysfunction (EED) is common in low- and middle-income countries and associated with childhood undernutrition. The composition of gut microbiota has been implicated in the pathogenesis of EED. Our aim was to assess the associations between gut microbiota and EED biomarkers in rural Malawian children. We hypothesized that there would be an inverse association between microbiota maturity and diversity and fecal concentrations of EED biomarkers. METHODS: We used data from fecal samples collected at 6, 18 and 30 months from 611 children who were followed up during a nutrition intervention trial. The primary time point for analysis was 18 months. Microbiota data were obtained through 16S rRNA sequencing and variables included microbiota maturity and diversity, phylogenetic dissimilarity and relative abundances of individual taxa. EED biomarkers included calprotectin (marker of inflammation), alpha-1 antitrypsin (intestinal permeability) and REG1B (intestinal damage). RESULTS: There was an inverse association between microbiota maturity and diversity and fecal concentrations of all 3 EED biomarkers at 18 months (p≤0.001). The results were similar at 30 months, while at 6 months inverse associations were found only with calprotectin and alpha-1 antitrypsin concentrations. At 18 months, EED biomarkers were not associated with phylogenetic dissimilarity, but at 6 and 30 months several associations were observed. Individual taxa predicting EED biomarker concentrations at 18 months included several Bifidobacterium and Enterobacteriaceae taxa as well as potentially displaced oral taxa. CONCLUSIONS: Our findings support the hypothesis of an inverse association between microbiota maturity and diversity and EED in rural Malawian children.
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spelling pubmed-88463642022-02-16 Associations between Gut Microbiota and Intestinal Inflammation, Permeability and Damage in Young Malawian Children Kortekangas, Emma Fan, Yue-Mei Chaima, David Lehto, Kirsi-Maarit Malamba-Banda, Chikondi Matchado, Andrew Chingwanda, Chilungamo Liu, Zhifei Ashorn, Ulla Cheung, Yin Bun Dewey, Kathryn G Maleta, Kenneth Ashorn, Per J Trop Pediatr Original Paper BACKGROUND: Environmental enteric dysfunction (EED) is common in low- and middle-income countries and associated with childhood undernutrition. The composition of gut microbiota has been implicated in the pathogenesis of EED. Our aim was to assess the associations between gut microbiota and EED biomarkers in rural Malawian children. We hypothesized that there would be an inverse association between microbiota maturity and diversity and fecal concentrations of EED biomarkers. METHODS: We used data from fecal samples collected at 6, 18 and 30 months from 611 children who were followed up during a nutrition intervention trial. The primary time point for analysis was 18 months. Microbiota data were obtained through 16S rRNA sequencing and variables included microbiota maturity and diversity, phylogenetic dissimilarity and relative abundances of individual taxa. EED biomarkers included calprotectin (marker of inflammation), alpha-1 antitrypsin (intestinal permeability) and REG1B (intestinal damage). RESULTS: There was an inverse association between microbiota maturity and diversity and fecal concentrations of all 3 EED biomarkers at 18 months (p≤0.001). The results were similar at 30 months, while at 6 months inverse associations were found only with calprotectin and alpha-1 antitrypsin concentrations. At 18 months, EED biomarkers were not associated with phylogenetic dissimilarity, but at 6 and 30 months several associations were observed. Individual taxa predicting EED biomarker concentrations at 18 months included several Bifidobacterium and Enterobacteriaceae taxa as well as potentially displaced oral taxa. CONCLUSIONS: Our findings support the hypothesis of an inverse association between microbiota maturity and diversity and EED in rural Malawian children. Oxford University Press 2022-02-12 /pmc/articles/PMC8846364/ /pubmed/35149871 http://dx.doi.org/10.1093/tropej/fmac012 Text en © The Author(s) [2022]. Published by Oxford University Press. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Paper
Kortekangas, Emma
Fan, Yue-Mei
Chaima, David
Lehto, Kirsi-Maarit
Malamba-Banda, Chikondi
Matchado, Andrew
Chingwanda, Chilungamo
Liu, Zhifei
Ashorn, Ulla
Cheung, Yin Bun
Dewey, Kathryn G
Maleta, Kenneth
Ashorn, Per
Associations between Gut Microbiota and Intestinal Inflammation, Permeability and Damage in Young Malawian Children
title Associations between Gut Microbiota and Intestinal Inflammation, Permeability and Damage in Young Malawian Children
title_full Associations between Gut Microbiota and Intestinal Inflammation, Permeability and Damage in Young Malawian Children
title_fullStr Associations between Gut Microbiota and Intestinal Inflammation, Permeability and Damage in Young Malawian Children
title_full_unstemmed Associations between Gut Microbiota and Intestinal Inflammation, Permeability and Damage in Young Malawian Children
title_short Associations between Gut Microbiota and Intestinal Inflammation, Permeability and Damage in Young Malawian Children
title_sort associations between gut microbiota and intestinal inflammation, permeability and damage in young malawian children
topic Original Paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8846364/
https://www.ncbi.nlm.nih.gov/pubmed/35149871
http://dx.doi.org/10.1093/tropej/fmac012
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