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Association of suboptimal health status with intestinal microbiota in Chinese youths
Suboptimal health status (SHS), a physical state between health and disease, is a subclinical and reversible stage of chronic disease. Previous studies have shown alterations in the intestinal microbiota in patients with some chronic diseases. This study aimed to investigate the association between...
Autores principales: | , , , , , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
John Wiley and Sons Inc.
2019
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6991644/ https://www.ncbi.nlm.nih.gov/pubmed/31808612 http://dx.doi.org/10.1111/jcmm.14880 |
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author | Sun, Qi Xu, Xizhu Zhang, Jie Sun, Ming Tian, Qiuyue Li, Qihuan Cao, Weijie Zhang, Xiaoyu Wang, Hao Liu, Jiaonan Zhang, Jinxia Meng, Xiaoni Wu, Lijuan Song, Manshu Liu, Hongqi Wang, Wei Wang, Youxin |
author_facet | Sun, Qi Xu, Xizhu Zhang, Jie Sun, Ming Tian, Qiuyue Li, Qihuan Cao, Weijie Zhang, Xiaoyu Wang, Hao Liu, Jiaonan Zhang, Jinxia Meng, Xiaoni Wu, Lijuan Song, Manshu Liu, Hongqi Wang, Wei Wang, Youxin |
author_sort | Sun, Qi |
collection | PubMed |
description | Suboptimal health status (SHS), a physical state between health and disease, is a subclinical and reversible stage of chronic disease. Previous studies have shown alterations in the intestinal microbiota in patients with some chronic diseases. This study aimed to investigate the association between SHS and intestinal microbiota in a case‐control study with 50 SHS individuals and 50 matched healthy controls. Intestinal microbiota was analysed by MiSeq 250PE. Alpha diversity of intestinal microbiota in SHS individuals was higher compared with that of healthy controls (Simpson index, W = 2238, P = .048). Beta diversity was different between SHS and healthy controls (P = .018). At the phylum level, the relative abundance of Verrucomicrobia was higher in the SHS group than that in the controls (W = 2201, P = .049). Compared with that of the control group, nine genera were significantly higher and five genera were lower in abundance in the SHS group (all P < .05). The intestinal microbiota, analysed by a random forest model, was able to distinguish individuals with SHS from the controls, with an area under the curve of 0.79 (95% confidence interval: 0.77‐0.81). We demonstrated that the alteration of intestinal microbiota occurs with SHS, an early stage of disease, which might shed light on the importance of intestinal microbiota in the primary prevention of noncommunicable chronic diseases. |
format | Online Article Text |
id | pubmed-6991644 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2019 |
publisher | John Wiley and Sons Inc. |
record_format | MEDLINE/PubMed |
spelling | pubmed-69916442020-02-03 Association of suboptimal health status with intestinal microbiota in Chinese youths Sun, Qi Xu, Xizhu Zhang, Jie Sun, Ming Tian, Qiuyue Li, Qihuan Cao, Weijie Zhang, Xiaoyu Wang, Hao Liu, Jiaonan Zhang, Jinxia Meng, Xiaoni Wu, Lijuan Song, Manshu Liu, Hongqi Wang, Wei Wang, Youxin J Cell Mol Med Original Articles Suboptimal health status (SHS), a physical state between health and disease, is a subclinical and reversible stage of chronic disease. Previous studies have shown alterations in the intestinal microbiota in patients with some chronic diseases. This study aimed to investigate the association between SHS and intestinal microbiota in a case‐control study with 50 SHS individuals and 50 matched healthy controls. Intestinal microbiota was analysed by MiSeq 250PE. Alpha diversity of intestinal microbiota in SHS individuals was higher compared with that of healthy controls (Simpson index, W = 2238, P = .048). Beta diversity was different between SHS and healthy controls (P = .018). At the phylum level, the relative abundance of Verrucomicrobia was higher in the SHS group than that in the controls (W = 2201, P = .049). Compared with that of the control group, nine genera were significantly higher and five genera were lower in abundance in the SHS group (all P < .05). The intestinal microbiota, analysed by a random forest model, was able to distinguish individuals with SHS from the controls, with an area under the curve of 0.79 (95% confidence interval: 0.77‐0.81). We demonstrated that the alteration of intestinal microbiota occurs with SHS, an early stage of disease, which might shed light on the importance of intestinal microbiota in the primary prevention of noncommunicable chronic diseases. John Wiley and Sons Inc. 2019-12-06 2020-01 /pmc/articles/PMC6991644/ /pubmed/31808612 http://dx.doi.org/10.1111/jcmm.14880 Text en © 2019 The Authors. Journal of Cellular and Molecular Medicine published by Foundation for Cellular and Molecular Medicine and John Wiley & Sons Ltd This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited. |
spellingShingle | Original Articles Sun, Qi Xu, Xizhu Zhang, Jie Sun, Ming Tian, Qiuyue Li, Qihuan Cao, Weijie Zhang, Xiaoyu Wang, Hao Liu, Jiaonan Zhang, Jinxia Meng, Xiaoni Wu, Lijuan Song, Manshu Liu, Hongqi Wang, Wei Wang, Youxin Association of suboptimal health status with intestinal microbiota in Chinese youths |
title | Association of suboptimal health status with intestinal microbiota in Chinese youths |
title_full | Association of suboptimal health status with intestinal microbiota in Chinese youths |
title_fullStr | Association of suboptimal health status with intestinal microbiota in Chinese youths |
title_full_unstemmed | Association of suboptimal health status with intestinal microbiota in Chinese youths |
title_short | Association of suboptimal health status with intestinal microbiota in Chinese youths |
title_sort | association of suboptimal health status with intestinal microbiota in chinese youths |
topic | Original Articles |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6991644/ https://www.ncbi.nlm.nih.gov/pubmed/31808612 http://dx.doi.org/10.1111/jcmm.14880 |
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