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Maternal fecal microbiome predicts gestational age, birth weight and neonatal growth in rural Zimbabwe.

BACKGROUND: Preterm birth and low birth weight (LBW) affect one in ten and one in seven livebirths, respectively, primarily in low-income and middle-income countries (LMIC) and are major predictors of poor child health outcomes. However, both have been recalcitrant to public health intervention. The...

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Autores principales: Gough, Ethan K., Edens, Thaddeus J., Geum, Hyun Min, Baharmand, Iman, Gill, Sandeep K., Robertson, Ruairi C., Mutasa, Kuda, Ntozini, Robert, Smith, Laura E, Chasekwa, Bernard, Majo, Florence D., Tavengwa, Naume V., Mutasa, Batsirai, Francis, Freddy, Carr, Lynnea, Tome, Joice, Stoltzfus, Rebecca J., Moulton, Lawrence H., Prendergast, Andrew J., Humphrey, Jean H., Manges, Amee R., Team, SHINE Trial
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217692/
https://www.ncbi.nlm.nih.gov/pubmed/34139432
http://dx.doi.org/10.1016/j.ebiom.2021.103421
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author Gough, Ethan K.
Edens, Thaddeus J.
Geum, Hyun Min
Baharmand, Iman
Gill, Sandeep K.
Robertson, Ruairi C.
Mutasa, Kuda
Ntozini, Robert
Smith, Laura E
Chasekwa, Bernard
Majo, Florence D.
Tavengwa, Naume V.
Mutasa, Batsirai
Francis, Freddy
Carr, Lynnea
Tome, Joice
Stoltzfus, Rebecca J.
Moulton, Lawrence H.
Prendergast, Andrew J.
Humphrey, Jean H.
Manges, Amee R.
Team, SHINE Trial
author_facet Gough, Ethan K.
Edens, Thaddeus J.
Geum, Hyun Min
Baharmand, Iman
Gill, Sandeep K.
Robertson, Ruairi C.
Mutasa, Kuda
Ntozini, Robert
Smith, Laura E
Chasekwa, Bernard
Majo, Florence D.
Tavengwa, Naume V.
Mutasa, Batsirai
Francis, Freddy
Carr, Lynnea
Tome, Joice
Stoltzfus, Rebecca J.
Moulton, Lawrence H.
Prendergast, Andrew J.
Humphrey, Jean H.
Manges, Amee R.
Team, SHINE Trial
author_sort Gough, Ethan K.
collection PubMed
description BACKGROUND: Preterm birth and low birth weight (LBW) affect one in ten and one in seven livebirths, respectively, primarily in low-income and middle-income countries (LMIC) and are major predictors of poor child health outcomes. However, both have been recalcitrant to public health intervention. The maternal intestinal microbiome may undergo substantial changes during pregnancy and may influence fetal and neonatal health in LMIC populations. METHODS: Within a subgroup of 207 mothers and infants enrolled in the SHINE trial in rural Zimbabwe, we performed shotgun metagenomics on 351 fecal specimens provided during pregnancy and at 1-month post-partum to investigate the relationship between the pregnancy gut microbiome and infant gestational age, birth weight, 1-month length-, and weight-for-age z-scores using extreme gradient boosting machines. FINDINGS: Pregnancy gut microbiome taxa and metabolic functions predicted birth weight and WAZ at 1 month more accurately than gestational age and LAZ. Blastoscystis sp, Brachyspira sp and Treponeme carriage were high compared to Western populations. Resistant starch-degraders were important predictors of birth outcomes. Microbiome capacity for environmental sensing, vitamin B metabolism, and signalling predicted increased infant birth weight and neonatal growth; while functions involved in biofilm formation in response to nutrient starvation predicted reduced birth weight and growth. INTERPRETATION: The pregnancy gut microbiome in rural Zimbabwe is characterized by resistant starch-degraders and may be an important metabolic target to improve birth weight. FUNDING: Bill and Melinda Gates Foundation, UK Department for International Development, Wellcome Trust, Swiss Agency for Development and Cooperation, US National Institutes of Health, and UNICEF.
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spelling pubmed-82176922021-06-28 Maternal fecal microbiome predicts gestational age, birth weight and neonatal growth in rural Zimbabwe. Gough, Ethan K. Edens, Thaddeus J. Geum, Hyun Min Baharmand, Iman Gill, Sandeep K. Robertson, Ruairi C. Mutasa, Kuda Ntozini, Robert Smith, Laura E Chasekwa, Bernard Majo, Florence D. Tavengwa, Naume V. Mutasa, Batsirai Francis, Freddy Carr, Lynnea Tome, Joice Stoltzfus, Rebecca J. Moulton, Lawrence H. Prendergast, Andrew J. Humphrey, Jean H. Manges, Amee R. Team, SHINE Trial EBioMedicine Research paper BACKGROUND: Preterm birth and low birth weight (LBW) affect one in ten and one in seven livebirths, respectively, primarily in low-income and middle-income countries (LMIC) and are major predictors of poor child health outcomes. However, both have been recalcitrant to public health intervention. The maternal intestinal microbiome may undergo substantial changes during pregnancy and may influence fetal and neonatal health in LMIC populations. METHODS: Within a subgroup of 207 mothers and infants enrolled in the SHINE trial in rural Zimbabwe, we performed shotgun metagenomics on 351 fecal specimens provided during pregnancy and at 1-month post-partum to investigate the relationship between the pregnancy gut microbiome and infant gestational age, birth weight, 1-month length-, and weight-for-age z-scores using extreme gradient boosting machines. FINDINGS: Pregnancy gut microbiome taxa and metabolic functions predicted birth weight and WAZ at 1 month more accurately than gestational age and LAZ. Blastoscystis sp, Brachyspira sp and Treponeme carriage were high compared to Western populations. Resistant starch-degraders were important predictors of birth outcomes. Microbiome capacity for environmental sensing, vitamin B metabolism, and signalling predicted increased infant birth weight and neonatal growth; while functions involved in biofilm formation in response to nutrient starvation predicted reduced birth weight and growth. INTERPRETATION: The pregnancy gut microbiome in rural Zimbabwe is characterized by resistant starch-degraders and may be an important metabolic target to improve birth weight. FUNDING: Bill and Melinda Gates Foundation, UK Department for International Development, Wellcome Trust, Swiss Agency for Development and Cooperation, US National Institutes of Health, and UNICEF. Elsevier 2021-06-15 /pmc/articles/PMC8217692/ /pubmed/34139432 http://dx.doi.org/10.1016/j.ebiom.2021.103421 Text en © 2021 The Author(s) https://creativecommons.org/licenses/by/4.0/This is an open access article under the CC BY license (http://creativecommons.org/licenses/by/4.0/).
spellingShingle Research paper
Gough, Ethan K.
Edens, Thaddeus J.
Geum, Hyun Min
Baharmand, Iman
Gill, Sandeep K.
Robertson, Ruairi C.
Mutasa, Kuda
Ntozini, Robert
Smith, Laura E
Chasekwa, Bernard
Majo, Florence D.
Tavengwa, Naume V.
Mutasa, Batsirai
Francis, Freddy
Carr, Lynnea
Tome, Joice
Stoltzfus, Rebecca J.
Moulton, Lawrence H.
Prendergast, Andrew J.
Humphrey, Jean H.
Manges, Amee R.
Team, SHINE Trial
Maternal fecal microbiome predicts gestational age, birth weight and neonatal growth in rural Zimbabwe.
title Maternal fecal microbiome predicts gestational age, birth weight and neonatal growth in rural Zimbabwe.
title_full Maternal fecal microbiome predicts gestational age, birth weight and neonatal growth in rural Zimbabwe.
title_fullStr Maternal fecal microbiome predicts gestational age, birth weight and neonatal growth in rural Zimbabwe.
title_full_unstemmed Maternal fecal microbiome predicts gestational age, birth weight and neonatal growth in rural Zimbabwe.
title_short Maternal fecal microbiome predicts gestational age, birth weight and neonatal growth in rural Zimbabwe.
title_sort maternal fecal microbiome predicts gestational age, birth weight and neonatal growth in rural zimbabwe.
topic Research paper
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8217692/
https://www.ncbi.nlm.nih.gov/pubmed/34139432
http://dx.doi.org/10.1016/j.ebiom.2021.103421
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