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Correlation of placental microbiota with fetal macrosomia and clinical characteristics in mothers and newborns
Substantial studies indicated that fetal macrosomia was associated with detrimental pregnancy outcomes, and increased susceptibility to metabolic diseases in later life. However, investigations into the association between placental microbiota and fetal macrosomia are limited. We aimed to profile th...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Impact Journals LLC
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669892/ https://www.ncbi.nlm.nih.gov/pubmed/29137266 http://dx.doi.org/10.18632/oncotarget.19319 |
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author | Zheng, Jia Xiao, Xin-Hua Zhang, Qian Mao, Li-Li Yu, Miao Xu, Jian-Ping Wang, Tong |
author_facet | Zheng, Jia Xiao, Xin-Hua Zhang, Qian Mao, Li-Li Yu, Miao Xu, Jian-Ping Wang, Tong |
author_sort | Zheng, Jia |
collection | PubMed |
description | Substantial studies indicated that fetal macrosomia was associated with detrimental pregnancy outcomes, and increased susceptibility to metabolic diseases in later life. However, investigations into the association between placental microbiota and fetal macrosomia are limited. We aimed to profile the placental microbiota of fetal macrosomia and study whether they relate to clinical characteristics. Placenta samples were collected from fetal macrosomias and newborns with normal birth weight. The clinical characteristics, umbilical cord blood parameters were measured, and placental microbiota were sequenced and further analysed. The clinical characteristics of infants and mothers and umbilical cord blood parameters were significantly different between macrosomias and controls. The relative abundance of microbiota sequences revealed that microbial structures of the placenta differed significantly between macrosomia and controls. Regression analysis showed a cluster of key operational taxonomic unit (OTUs), phyla and genera were significantly correlated with body length, ponderal index and placenta weight, body weight increase during pregnancy of mothers, and cord blood IGF-1 and leptin concentrations. In conclusion, our study for the first time explored the relationship between placental microbiota profile and fetal macrosomia. It is novel in showing that a distinct placental microbiota profile is present in fetal macrosomia, and is associated with clinical characteristics of mothers and newborns. |
format | Online Article Text |
id | pubmed-5669892 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Impact Journals LLC |
record_format | MEDLINE/PubMed |
spelling | pubmed-56698922017-11-09 Correlation of placental microbiota with fetal macrosomia and clinical characteristics in mothers and newborns Zheng, Jia Xiao, Xin-Hua Zhang, Qian Mao, Li-Li Yu, Miao Xu, Jian-Ping Wang, Tong Oncotarget Research Paper Substantial studies indicated that fetal macrosomia was associated with detrimental pregnancy outcomes, and increased susceptibility to metabolic diseases in later life. However, investigations into the association between placental microbiota and fetal macrosomia are limited. We aimed to profile the placental microbiota of fetal macrosomia and study whether they relate to clinical characteristics. Placenta samples were collected from fetal macrosomias and newborns with normal birth weight. The clinical characteristics, umbilical cord blood parameters were measured, and placental microbiota were sequenced and further analysed. The clinical characteristics of infants and mothers and umbilical cord blood parameters were significantly different between macrosomias and controls. The relative abundance of microbiota sequences revealed that microbial structures of the placenta differed significantly between macrosomia and controls. Regression analysis showed a cluster of key operational taxonomic unit (OTUs), phyla and genera were significantly correlated with body length, ponderal index and placenta weight, body weight increase during pregnancy of mothers, and cord blood IGF-1 and leptin concentrations. In conclusion, our study for the first time explored the relationship between placental microbiota profile and fetal macrosomia. It is novel in showing that a distinct placental microbiota profile is present in fetal macrosomia, and is associated with clinical characteristics of mothers and newborns. Impact Journals LLC 2017-07-18 /pmc/articles/PMC5669892/ /pubmed/29137266 http://dx.doi.org/10.18632/oncotarget.19319 Text en Copyright: © 2017 Zheng et al. http://creativecommons.org/licenses/by/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by/3.0/) 3.0 (CC BY 3.0), which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are credited. |
spellingShingle | Research Paper Zheng, Jia Xiao, Xin-Hua Zhang, Qian Mao, Li-Li Yu, Miao Xu, Jian-Ping Wang, Tong Correlation of placental microbiota with fetal macrosomia and clinical characteristics in mothers and newborns |
title | Correlation of placental microbiota with fetal macrosomia and clinical characteristics in mothers and newborns |
title_full | Correlation of placental microbiota with fetal macrosomia and clinical characteristics in mothers and newborns |
title_fullStr | Correlation of placental microbiota with fetal macrosomia and clinical characteristics in mothers and newborns |
title_full_unstemmed | Correlation of placental microbiota with fetal macrosomia and clinical characteristics in mothers and newborns |
title_short | Correlation of placental microbiota with fetal macrosomia and clinical characteristics in mothers and newborns |
title_sort | correlation of placental microbiota with fetal macrosomia and clinical characteristics in mothers and newborns |
topic | Research Paper |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5669892/ https://www.ncbi.nlm.nih.gov/pubmed/29137266 http://dx.doi.org/10.18632/oncotarget.19319 |
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