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Dysbiosis of the intestinal microbiota in neurocritically ill patients and the risk for death

BACKGROUND: Despite the essential functions of the intestinal microbiota in human physiology, little has been reported about the microbiome in neurocritically ill patients. This investigation aimed to evaluate the characteristics of the gut microbiome in neurocritically ill patients and its changes...

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Autores principales: Xu, Ruoting, Tan, Chuhong, Zhu, Jiajia, Zeng, Xiuli, Gao, Xuxuan, Wu, Qiheng, Chen, Qiong, Wang, Huidi, Zhou, Hongwei, He, Yan, Pan, Suyue, Yin, Jia
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2019
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544929/
https://www.ncbi.nlm.nih.gov/pubmed/31151471
http://dx.doi.org/10.1186/s13054-019-2488-4
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author Xu, Ruoting
Tan, Chuhong
Zhu, Jiajia
Zeng, Xiuli
Gao, Xuxuan
Wu, Qiheng
Chen, Qiong
Wang, Huidi
Zhou, Hongwei
He, Yan
Pan, Suyue
Yin, Jia
author_facet Xu, Ruoting
Tan, Chuhong
Zhu, Jiajia
Zeng, Xiuli
Gao, Xuxuan
Wu, Qiheng
Chen, Qiong
Wang, Huidi
Zhou, Hongwei
He, Yan
Pan, Suyue
Yin, Jia
author_sort Xu, Ruoting
collection PubMed
description BACKGROUND: Despite the essential functions of the intestinal microbiota in human physiology, little has been reported about the microbiome in neurocritically ill patients. This investigation aimed to evaluate the characteristics of the gut microbiome in neurocritically ill patients and its changes after admission. Furthermore, we investigated whether the characteristics of the gut microbiome at admission were a risk factor for death within 180 days. METHODS: This prospective observational cohort study included neurocritically ill patients admitted to the neurological intensive care unit of a large university-affiliated academic hospital in Guangzhou. Faecal samples were collected within 72 h after admission (before antibiotic treatment) and serially each week. Healthy volunteers were recruited from a community in Guangzhou. The gut microbiome was monitored via 16S rRNA gene sequence analysis, and the associations with the clinical outcome were evaluated by a Cox proportional hazards model. RESULTS: In total, 98 patients and 84 age- and sex-matched healthy subjects were included in the analysis. Compared with healthy subjects, the neurocritically ill patients exhibited significantly different compositions of intestinal microbiota. During hospitalization, the α-diversity and abundance of Ruminococcaceae and Lachnospiraceae decreased significantly over time in patients followed longitudinally. The abundance of Enterobacteriaceae was positively associated with the modified Rankin Scale at discharge. In the multivariate Cox regression analysis, Christensenellaceae and Erysipelotrichaceae were associated with an increased risk of death. The increases in intestinal Enterobacteriales and Enterobacteriaceae during the first week in the neurological intensive care unit were associated with increases of 92% in the risk of 180-day mortality after adjustments. CONCLUSIONS: This analysis of the gut microbiome in 98 neurocritically ill patients indicates that the gut microbiota composition in these patients differs significantly from that in a healthy population and that the magnitude of this dysbiosis increases during hospitalization in a neurological intensive care unit. The gut microbiota characteristics seem to have an impact on patients’ 180-day mortality. Gut microbiota analysis could hopefully predict outcome in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2488-4) contains supplementary material, which is available to authorized users.
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spelling pubmed-65449292019-06-04 Dysbiosis of the intestinal microbiota in neurocritically ill patients and the risk for death Xu, Ruoting Tan, Chuhong Zhu, Jiajia Zeng, Xiuli Gao, Xuxuan Wu, Qiheng Chen, Qiong Wang, Huidi Zhou, Hongwei He, Yan Pan, Suyue Yin, Jia Crit Care Research BACKGROUND: Despite the essential functions of the intestinal microbiota in human physiology, little has been reported about the microbiome in neurocritically ill patients. This investigation aimed to evaluate the characteristics of the gut microbiome in neurocritically ill patients and its changes after admission. Furthermore, we investigated whether the characteristics of the gut microbiome at admission were a risk factor for death within 180 days. METHODS: This prospective observational cohort study included neurocritically ill patients admitted to the neurological intensive care unit of a large university-affiliated academic hospital in Guangzhou. Faecal samples were collected within 72 h after admission (before antibiotic treatment) and serially each week. Healthy volunteers were recruited from a community in Guangzhou. The gut microbiome was monitored via 16S rRNA gene sequence analysis, and the associations with the clinical outcome were evaluated by a Cox proportional hazards model. RESULTS: In total, 98 patients and 84 age- and sex-matched healthy subjects were included in the analysis. Compared with healthy subjects, the neurocritically ill patients exhibited significantly different compositions of intestinal microbiota. During hospitalization, the α-diversity and abundance of Ruminococcaceae and Lachnospiraceae decreased significantly over time in patients followed longitudinally. The abundance of Enterobacteriaceae was positively associated with the modified Rankin Scale at discharge. In the multivariate Cox regression analysis, Christensenellaceae and Erysipelotrichaceae were associated with an increased risk of death. The increases in intestinal Enterobacteriales and Enterobacteriaceae during the first week in the neurological intensive care unit were associated with increases of 92% in the risk of 180-day mortality after adjustments. CONCLUSIONS: This analysis of the gut microbiome in 98 neurocritically ill patients indicates that the gut microbiota composition in these patients differs significantly from that in a healthy population and that the magnitude of this dysbiosis increases during hospitalization in a neurological intensive care unit. The gut microbiota characteristics seem to have an impact on patients’ 180-day mortality. Gut microbiota analysis could hopefully predict outcome in the future. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s13054-019-2488-4) contains supplementary material, which is available to authorized users. BioMed Central 2019-05-31 /pmc/articles/PMC6544929/ /pubmed/31151471 http://dx.doi.org/10.1186/s13054-019-2488-4 Text en © The Author(s). 2019 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Xu, Ruoting
Tan, Chuhong
Zhu, Jiajia
Zeng, Xiuli
Gao, Xuxuan
Wu, Qiheng
Chen, Qiong
Wang, Huidi
Zhou, Hongwei
He, Yan
Pan, Suyue
Yin, Jia
Dysbiosis of the intestinal microbiota in neurocritically ill patients and the risk for death
title Dysbiosis of the intestinal microbiota in neurocritically ill patients and the risk for death
title_full Dysbiosis of the intestinal microbiota in neurocritically ill patients and the risk for death
title_fullStr Dysbiosis of the intestinal microbiota in neurocritically ill patients and the risk for death
title_full_unstemmed Dysbiosis of the intestinal microbiota in neurocritically ill patients and the risk for death
title_short Dysbiosis of the intestinal microbiota in neurocritically ill patients and the risk for death
title_sort dysbiosis of the intestinal microbiota in neurocritically ill patients and the risk for death
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6544929/
https://www.ncbi.nlm.nih.gov/pubmed/31151471
http://dx.doi.org/10.1186/s13054-019-2488-4
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