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Gestational Diabetes Is Uniquely Associated With Altered Early Seeding of the Infant Gut Microbiota

Gestational diabetes mellitus (GDM) is a worldwide public health problem affecting up to 27% of pregnancies with high predictive values for childhood obesity and inflammatory diseases. Compromised seeding of the infant gut microbiota is a risk factor for immunologic and metabolic diseases in the off...

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Autores principales: Soderborg, Taylor K., Carpenter, Charles M., Janssen, Rachel C., Weir, Tiffany L., Robertson, Charles E., Ir, Diana, Young, Bridget E., Krebs, Nancy F., Hernandez, Teri L., Barbour, Linda A., Frank, Daniel N., Kroehl, Miranda, Friedman, Jacob E.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729132/
https://www.ncbi.nlm.nih.gov/pubmed/33329403
http://dx.doi.org/10.3389/fendo.2020.603021
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author Soderborg, Taylor K.
Carpenter, Charles M.
Janssen, Rachel C.
Weir, Tiffany L.
Robertson, Charles E.
Ir, Diana
Young, Bridget E.
Krebs, Nancy F.
Hernandez, Teri L.
Barbour, Linda A.
Frank, Daniel N.
Kroehl, Miranda
Friedman, Jacob E.
author_facet Soderborg, Taylor K.
Carpenter, Charles M.
Janssen, Rachel C.
Weir, Tiffany L.
Robertson, Charles E.
Ir, Diana
Young, Bridget E.
Krebs, Nancy F.
Hernandez, Teri L.
Barbour, Linda A.
Frank, Daniel N.
Kroehl, Miranda
Friedman, Jacob E.
author_sort Soderborg, Taylor K.
collection PubMed
description Gestational diabetes mellitus (GDM) is a worldwide public health problem affecting up to 27% of pregnancies with high predictive values for childhood obesity and inflammatory diseases. Compromised seeding of the infant gut microbiota is a risk factor for immunologic and metabolic diseases in the offspring; however, how GDM along with maternal obesity interact to alter colonization remains unknown. We hypothesized that GDM individually and in combination with maternal overweight/obesity would alter gut microbial composition, diversity, and short-chain fatty acid (SCFA) levels in neonates. We investigated 46 full-term neonates born to normal-weight or overweight/obese mothers with and without GDM, accounting for confounders including cesarean delivery, lack of breastfeeding, and exposure to antibiotics. Gut microbiota in 2-week-old neonates born to mothers with GDM exhibited differences in abundance of 26 microbial taxa; 14 of which showed persistent differential abundance after adjusting for pre-pregnancy BMI. Key pioneering gut taxa, including potentially important taxa for establishing neonatal immunity, were reduced. Lactobacillus, Flavonifractor, Erysipelotrichaceae, and unspecified families in Gammaproteobacteria were significantly reduced in neonates from mothers with GDM. GDM was associated with an increase in microbes involved in suppressing early immune cell function (Phascolarctobacterium). No differences in infant stool SCFA levels by maternal phenotype were noted; however, significant correlations were found between microbial abundances and SCFA levels in neonates. Our results suggest that GDM alone and together with maternal overweight/obesity uniquely influences seeding of specific infant microbiota in patterns that set the stage for future risk of inflammatory and metabolic disease.
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spelling pubmed-77291322020-12-15 Gestational Diabetes Is Uniquely Associated With Altered Early Seeding of the Infant Gut Microbiota Soderborg, Taylor K. Carpenter, Charles M. Janssen, Rachel C. Weir, Tiffany L. Robertson, Charles E. Ir, Diana Young, Bridget E. Krebs, Nancy F. Hernandez, Teri L. Barbour, Linda A. Frank, Daniel N. Kroehl, Miranda Friedman, Jacob E. Front Endocrinol (Lausanne) Endocrinology Gestational diabetes mellitus (GDM) is a worldwide public health problem affecting up to 27% of pregnancies with high predictive values for childhood obesity and inflammatory diseases. Compromised seeding of the infant gut microbiota is a risk factor for immunologic and metabolic diseases in the offspring; however, how GDM along with maternal obesity interact to alter colonization remains unknown. We hypothesized that GDM individually and in combination with maternal overweight/obesity would alter gut microbial composition, diversity, and short-chain fatty acid (SCFA) levels in neonates. We investigated 46 full-term neonates born to normal-weight or overweight/obese mothers with and without GDM, accounting for confounders including cesarean delivery, lack of breastfeeding, and exposure to antibiotics. Gut microbiota in 2-week-old neonates born to mothers with GDM exhibited differences in abundance of 26 microbial taxa; 14 of which showed persistent differential abundance after adjusting for pre-pregnancy BMI. Key pioneering gut taxa, including potentially important taxa for establishing neonatal immunity, were reduced. Lactobacillus, Flavonifractor, Erysipelotrichaceae, and unspecified families in Gammaproteobacteria were significantly reduced in neonates from mothers with GDM. GDM was associated with an increase in microbes involved in suppressing early immune cell function (Phascolarctobacterium). No differences in infant stool SCFA levels by maternal phenotype were noted; however, significant correlations were found between microbial abundances and SCFA levels in neonates. Our results suggest that GDM alone and together with maternal overweight/obesity uniquely influences seeding of specific infant microbiota in patterns that set the stage for future risk of inflammatory and metabolic disease. Frontiers Media S.A. 2020-11-27 /pmc/articles/PMC7729132/ /pubmed/33329403 http://dx.doi.org/10.3389/fendo.2020.603021 Text en Copyright © 2020 Soderborg, Carpenter, Janssen, Weir, Robertson, Ir, Young, Krebs, Hernandez, Barbour, Frank, Kroehl and Friedman http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) and the copyright owner(s) are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.
spellingShingle Endocrinology
Soderborg, Taylor K.
Carpenter, Charles M.
Janssen, Rachel C.
Weir, Tiffany L.
Robertson, Charles E.
Ir, Diana
Young, Bridget E.
Krebs, Nancy F.
Hernandez, Teri L.
Barbour, Linda A.
Frank, Daniel N.
Kroehl, Miranda
Friedman, Jacob E.
Gestational Diabetes Is Uniquely Associated With Altered Early Seeding of the Infant Gut Microbiota
title Gestational Diabetes Is Uniquely Associated With Altered Early Seeding of the Infant Gut Microbiota
title_full Gestational Diabetes Is Uniquely Associated With Altered Early Seeding of the Infant Gut Microbiota
title_fullStr Gestational Diabetes Is Uniquely Associated With Altered Early Seeding of the Infant Gut Microbiota
title_full_unstemmed Gestational Diabetes Is Uniquely Associated With Altered Early Seeding of the Infant Gut Microbiota
title_short Gestational Diabetes Is Uniquely Associated With Altered Early Seeding of the Infant Gut Microbiota
title_sort gestational diabetes is uniquely associated with altered early seeding of the infant gut microbiota
topic Endocrinology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7729132/
https://www.ncbi.nlm.nih.gov/pubmed/33329403
http://dx.doi.org/10.3389/fendo.2020.603021
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