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Human Milk Oligosaccharides and Bacterial Profile Modulate Infant Body Composition during Exclusive Breastfeeding
Human milk is a complex and variable ecosystem fundamental to the development of newborns. This study aimed to investigate relationships between human milk oligosaccharides (HMO) and human milk bacterial profiles and infant body composition. Human milk samples (n = 60) were collected at two months p...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911220/ https://www.ncbi.nlm.nih.gov/pubmed/35270006 http://dx.doi.org/10.3390/ijms23052865 |
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author | Cheema, Ali S. Gridneva, Zoya Furst, Annalee J. Roman, Ana S. Trevenen, Michelle L. Turlach, Berwin A. Lai, Ching T. Stinson, Lisa F. Bode, Lars Payne, Matthew S. Geddes, Donna T. |
author_facet | Cheema, Ali S. Gridneva, Zoya Furst, Annalee J. Roman, Ana S. Trevenen, Michelle L. Turlach, Berwin A. Lai, Ching T. Stinson, Lisa F. Bode, Lars Payne, Matthew S. Geddes, Donna T. |
author_sort | Cheema, Ali S. |
collection | PubMed |
description | Human milk is a complex and variable ecosystem fundamental to the development of newborns. This study aimed to investigate relationships between human milk oligosaccharides (HMO) and human milk bacterial profiles and infant body composition. Human milk samples (n = 60) were collected at two months postpartum. Infant and maternal body composition was measured with bioimpedance spectroscopy. Human milk bacterial profiles were assessed using full-length 16S rRNA gene sequencing and 19 HMOs were quantitated using high-performance liquid chromatography. Relative abundance of human milk bacterial taxa were significantly associated with concentrations of several fucosylated and sialylated HMOs. Individual human milk bacteria and HMO intakes and concentrations were also significantly associated with infant anthropometry, fat-free mass, and adiposity. Furthermore, when data were stratified based on maternal secretor status, some of these relationships differed significantly among infants born to secretor vs non-secretor mothers. In conclusion, in this pilot study the human milk bacterial profile and HMO intakes and concentrations were significantly associated with infant body composition, with associations modified by secretor status. Future research designed to increase the understanding of the mechanisms by which HMO and human milk bacteria modulate infant body composition should include intakes in addition to concentrations. |
format | Online Article Text |
id | pubmed-8911220 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-89112202022-03-11 Human Milk Oligosaccharides and Bacterial Profile Modulate Infant Body Composition during Exclusive Breastfeeding Cheema, Ali S. Gridneva, Zoya Furst, Annalee J. Roman, Ana S. Trevenen, Michelle L. Turlach, Berwin A. Lai, Ching T. Stinson, Lisa F. Bode, Lars Payne, Matthew S. Geddes, Donna T. Int J Mol Sci Article Human milk is a complex and variable ecosystem fundamental to the development of newborns. This study aimed to investigate relationships between human milk oligosaccharides (HMO) and human milk bacterial profiles and infant body composition. Human milk samples (n = 60) were collected at two months postpartum. Infant and maternal body composition was measured with bioimpedance spectroscopy. Human milk bacterial profiles were assessed using full-length 16S rRNA gene sequencing and 19 HMOs were quantitated using high-performance liquid chromatography. Relative abundance of human milk bacterial taxa were significantly associated with concentrations of several fucosylated and sialylated HMOs. Individual human milk bacteria and HMO intakes and concentrations were also significantly associated with infant anthropometry, fat-free mass, and adiposity. Furthermore, when data were stratified based on maternal secretor status, some of these relationships differed significantly among infants born to secretor vs non-secretor mothers. In conclusion, in this pilot study the human milk bacterial profile and HMO intakes and concentrations were significantly associated with infant body composition, with associations modified by secretor status. Future research designed to increase the understanding of the mechanisms by which HMO and human milk bacteria modulate infant body composition should include intakes in addition to concentrations. MDPI 2022-03-05 /pmc/articles/PMC8911220/ /pubmed/35270006 http://dx.doi.org/10.3390/ijms23052865 Text en © 2022 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Article Cheema, Ali S. Gridneva, Zoya Furst, Annalee J. Roman, Ana S. Trevenen, Michelle L. Turlach, Berwin A. Lai, Ching T. Stinson, Lisa F. Bode, Lars Payne, Matthew S. Geddes, Donna T. Human Milk Oligosaccharides and Bacterial Profile Modulate Infant Body Composition during Exclusive Breastfeeding |
title | Human Milk Oligosaccharides and Bacterial Profile Modulate Infant Body Composition during Exclusive Breastfeeding |
title_full | Human Milk Oligosaccharides and Bacterial Profile Modulate Infant Body Composition during Exclusive Breastfeeding |
title_fullStr | Human Milk Oligosaccharides and Bacterial Profile Modulate Infant Body Composition during Exclusive Breastfeeding |
title_full_unstemmed | Human Milk Oligosaccharides and Bacterial Profile Modulate Infant Body Composition during Exclusive Breastfeeding |
title_short | Human Milk Oligosaccharides and Bacterial Profile Modulate Infant Body Composition during Exclusive Breastfeeding |
title_sort | human milk oligosaccharides and bacterial profile modulate infant body composition during exclusive breastfeeding |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8911220/ https://www.ncbi.nlm.nih.gov/pubmed/35270006 http://dx.doi.org/10.3390/ijms23052865 |
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