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The association of gut microbiota characteristics in Malawian infants with growth and inflammation

We tested the hypotheses that a more mature or diverse gut microbiota will be positively associated with infant growth and inversely associated with inflammation. We characterized gut microbiota from the stool samples of Malawian infants at 6 mo (n = 527), 12 mo (n = 632) and 18 mo (n = 629) of age....

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Autores principales: Kamng’ona, Arox W., Young, Rebecca, Arnold, Charles D., Kortekangas, Emma, Patson, Noel, Jorgensen, Josh M., Prado, Elizabeth L., Chaima, David, Malamba, Chikondi, Ashorn, Ulla, Fan, Yue-Mei, Cheung, Yin B., Ashorn, Per, Maleta, Kenneth, Dewey, Kathryn G.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group UK 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733848/
https://www.ncbi.nlm.nih.gov/pubmed/31501455
http://dx.doi.org/10.1038/s41598-019-49274-y
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author Kamng’ona, Arox W.
Young, Rebecca
Arnold, Charles D.
Kortekangas, Emma
Patson, Noel
Jorgensen, Josh M.
Prado, Elizabeth L.
Chaima, David
Malamba, Chikondi
Ashorn, Ulla
Fan, Yue-Mei
Cheung, Yin B.
Ashorn, Per
Maleta, Kenneth
Dewey, Kathryn G.
author_facet Kamng’ona, Arox W.
Young, Rebecca
Arnold, Charles D.
Kortekangas, Emma
Patson, Noel
Jorgensen, Josh M.
Prado, Elizabeth L.
Chaima, David
Malamba, Chikondi
Ashorn, Ulla
Fan, Yue-Mei
Cheung, Yin B.
Ashorn, Per
Maleta, Kenneth
Dewey, Kathryn G.
author_sort Kamng’ona, Arox W.
collection PubMed
description We tested the hypotheses that a more mature or diverse gut microbiota will be positively associated with infant growth and inversely associated with inflammation. We characterized gut microbiota from the stool samples of Malawian infants at 6 mo (n = 527), 12 mo (n = 632) and 18 mo (n = 629) of age. Microbiota diversity and maturity measurements were based on Shannon diversity index and microbiota for age Z-score (MAZ), respectively. Growth was calculated as change in Z-scores for weight-for-age (WAZ), length-for-age (LAZ) and head circumference-for-age (HCZ) from 6 to 12 mo and 12 to 18 mo. Biomarkers of inflammation (alpha-1-acid glycoprotein (AGP) and C-reactive protein (CRP)) were measured at 6 and 18 mo. Multivariable models were used to assess the association of each independent variable with each outcome. Microbiota diversity and maturity were related to growth in weight from 6 to 12 mo, but not to growth in length or head circumference or to growth from 12 to 18 mo. Microbiota diversity and maturity may also be linked to inflammation, but findings were inconsistent.
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spelling pubmed-67338482019-09-20 The association of gut microbiota characteristics in Malawian infants with growth and inflammation Kamng’ona, Arox W. Young, Rebecca Arnold, Charles D. Kortekangas, Emma Patson, Noel Jorgensen, Josh M. Prado, Elizabeth L. Chaima, David Malamba, Chikondi Ashorn, Ulla Fan, Yue-Mei Cheung, Yin B. Ashorn, Per Maleta, Kenneth Dewey, Kathryn G. Sci Rep Article We tested the hypotheses that a more mature or diverse gut microbiota will be positively associated with infant growth and inversely associated with inflammation. We characterized gut microbiota from the stool samples of Malawian infants at 6 mo (n = 527), 12 mo (n = 632) and 18 mo (n = 629) of age. Microbiota diversity and maturity measurements were based on Shannon diversity index and microbiota for age Z-score (MAZ), respectively. Growth was calculated as change in Z-scores for weight-for-age (WAZ), length-for-age (LAZ) and head circumference-for-age (HCZ) from 6 to 12 mo and 12 to 18 mo. Biomarkers of inflammation (alpha-1-acid glycoprotein (AGP) and C-reactive protein (CRP)) were measured at 6 and 18 mo. Multivariable models were used to assess the association of each independent variable with each outcome. Microbiota diversity and maturity were related to growth in weight from 6 to 12 mo, but not to growth in length or head circumference or to growth from 12 to 18 mo. Microbiota diversity and maturity may also be linked to inflammation, but findings were inconsistent. Nature Publishing Group UK 2019-09-09 /pmc/articles/PMC6733848/ /pubmed/31501455 http://dx.doi.org/10.1038/s41598-019-49274-y Text en © The Author(s) 2019 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as 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 images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.
spellingShingle Article
Kamng’ona, Arox W.
Young, Rebecca
Arnold, Charles D.
Kortekangas, Emma
Patson, Noel
Jorgensen, Josh M.
Prado, Elizabeth L.
Chaima, David
Malamba, Chikondi
Ashorn, Ulla
Fan, Yue-Mei
Cheung, Yin B.
Ashorn, Per
Maleta, Kenneth
Dewey, Kathryn G.
The association of gut microbiota characteristics in Malawian infants with growth and inflammation
title The association of gut microbiota characteristics in Malawian infants with growth and inflammation
title_full The association of gut microbiota characteristics in Malawian infants with growth and inflammation
title_fullStr The association of gut microbiota characteristics in Malawian infants with growth and inflammation
title_full_unstemmed The association of gut microbiota characteristics in Malawian infants with growth and inflammation
title_short The association of gut microbiota characteristics in Malawian infants with growth and inflammation
title_sort association of gut microbiota characteristics in malawian infants with growth and inflammation
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6733848/
https://www.ncbi.nlm.nih.gov/pubmed/31501455
http://dx.doi.org/10.1038/s41598-019-49274-y
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