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Insight Into the Potential Value of Gut Microbial Signatures for Prediction of Gestational Anemia

The gut microbiota alternations are associated with gestational anemia (GA); however, limited predictive value for the subsequent incidence of anemia in normal gestational women has been obtained. We sought to rigorously characterise gut dysbiosis in subjects with GA and explored the potential predi...

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Autores principales: Wei, Hongcheng, Deng, Siting, Qin, Yufeng, Yang, Xu, Chen, Ting, Wang, Xu, Xia, Yankai
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Frontiers Media S.A. 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8437374/
https://www.ncbi.nlm.nih.gov/pubmed/34527605
http://dx.doi.org/10.3389/fcimb.2021.734561
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author Wei, Hongcheng
Deng, Siting
Qin, Yufeng
Yang, Xu
Chen, Ting
Wang, Xu
Xia, Yankai
author_facet Wei, Hongcheng
Deng, Siting
Qin, Yufeng
Yang, Xu
Chen, Ting
Wang, Xu
Xia, Yankai
author_sort Wei, Hongcheng
collection PubMed
description The gut microbiota alternations are associated with gestational anemia (GA); however, limited predictive value for the subsequent incidence of anemia in normal gestational women has been obtained. We sought to rigorously characterise gut dysbiosis in subjects with GA and explored the potential predictive value of novel microbial signatures for the risk of developing GA. A prospective cohort of subjects with GA (n = 156) and healthy control (n = 402), all of whom were free of GA in the second trimester, by 16S rRNA gene sequencing was conducted. Microbial signatures altered dramatically in GA compared with healthy control in the second trimester. Megamonas, Veillonella, and Haemophilus were confirmed to show differential abundances in GA after adjusting for covariates. On the contrary, Lachnospiraceae and Blautia were enriched in control. Microbial co-abundance group (CAG) network was constructed. Prospectively, CAG network relatively accurately predicted upcoming GA in normal pregnant women with an AUC of 0.7738 (95%CI: 0.7171, 0.8306) and the performance was further validated in Validation set (0.8223, 95%CI: 0.7573, 0.8874). Overall, our study demonstrated that alterations in the gut microbial community were associated with anemia in pregnancy and microbial signatures could accurately predict the subsequent incidence of anemia in normal pregnant women. Our findings provided new insights into understanding the role of gut microbiota in GA, identifying high-risk individuals, and modulating gut microbiota as a therapeutic target, thus improving quality of life and well-being of women and children.
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spelling pubmed-84373742021-09-14 Insight Into the Potential Value of Gut Microbial Signatures for Prediction of Gestational Anemia Wei, Hongcheng Deng, Siting Qin, Yufeng Yang, Xu Chen, Ting Wang, Xu Xia, Yankai Front Cell Infect Microbiol Cellular and Infection Microbiology The gut microbiota alternations are associated with gestational anemia (GA); however, limited predictive value for the subsequent incidence of anemia in normal gestational women has been obtained. We sought to rigorously characterise gut dysbiosis in subjects with GA and explored the potential predictive value of novel microbial signatures for the risk of developing GA. A prospective cohort of subjects with GA (n = 156) and healthy control (n = 402), all of whom were free of GA in the second trimester, by 16S rRNA gene sequencing was conducted. Microbial signatures altered dramatically in GA compared with healthy control in the second trimester. Megamonas, Veillonella, and Haemophilus were confirmed to show differential abundances in GA after adjusting for covariates. On the contrary, Lachnospiraceae and Blautia were enriched in control. Microbial co-abundance group (CAG) network was constructed. Prospectively, CAG network relatively accurately predicted upcoming GA in normal pregnant women with an AUC of 0.7738 (95%CI: 0.7171, 0.8306) and the performance was further validated in Validation set (0.8223, 95%CI: 0.7573, 0.8874). Overall, our study demonstrated that alterations in the gut microbial community were associated with anemia in pregnancy and microbial signatures could accurately predict the subsequent incidence of anemia in normal pregnant women. Our findings provided new insights into understanding the role of gut microbiota in GA, identifying high-risk individuals, and modulating gut microbiota as a therapeutic target, thus improving quality of life and well-being of women and children. Frontiers Media S.A. 2021-08-30 /pmc/articles/PMC8437374/ /pubmed/34527605 http://dx.doi.org/10.3389/fcimb.2021.734561 Text en Copyright © 2021 Wei, Deng, Qin, Yang, Chen, Wang and Xia https://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 Cellular and Infection Microbiology
Wei, Hongcheng
Deng, Siting
Qin, Yufeng
Yang, Xu
Chen, Ting
Wang, Xu
Xia, Yankai
Insight Into the Potential Value of Gut Microbial Signatures for Prediction of Gestational Anemia
title Insight Into the Potential Value of Gut Microbial Signatures for Prediction of Gestational Anemia
title_full Insight Into the Potential Value of Gut Microbial Signatures for Prediction of Gestational Anemia
title_fullStr Insight Into the Potential Value of Gut Microbial Signatures for Prediction of Gestational Anemia
title_full_unstemmed Insight Into the Potential Value of Gut Microbial Signatures for Prediction of Gestational Anemia
title_short Insight Into the Potential Value of Gut Microbial Signatures for Prediction of Gestational Anemia
title_sort insight into the potential value of gut microbial signatures for prediction of gestational anemia
topic Cellular and Infection Microbiology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8437374/
https://www.ncbi.nlm.nih.gov/pubmed/34527605
http://dx.doi.org/10.3389/fcimb.2021.734561
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