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Gut Microbiota and Liver Fibrosis: One Potential Biomarker for Predicting Liver Fibrosis

PURPOSE: To investigate the relationship between gut microbiota and liver fibrosis and establish a microbiota biomarker for detecting and staging liver fibrosis. METHODS: 131 Wistar rats were used in our study, and liver fibrosis was induced by carbon tetrachloride. Stool samples were collected with...

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Autores principales: Li, Zhiming, Ni, Ming, Yu, Haiyang, Wang, Lili, Zhou, Xiaoming, Chen, Tao, Liu, Guangzhen, Gao, Yuanxiang
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi 2020
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322594/
https://www.ncbi.nlm.nih.gov/pubmed/32685479
http://dx.doi.org/10.1155/2020/3905130
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author Li, Zhiming
Ni, Ming
Yu, Haiyang
Wang, Lili
Zhou, Xiaoming
Chen, Tao
Liu, Guangzhen
Gao, Yuanxiang
author_facet Li, Zhiming
Ni, Ming
Yu, Haiyang
Wang, Lili
Zhou, Xiaoming
Chen, Tao
Liu, Guangzhen
Gao, Yuanxiang
author_sort Li, Zhiming
collection PubMed
description PURPOSE: To investigate the relationship between gut microbiota and liver fibrosis and establish a microbiota biomarker for detecting and staging liver fibrosis. METHODS: 131 Wistar rats were used in our study, and liver fibrosis was induced by carbon tetrachloride. Stool samples were collected within 72 hours after the last administration. The V4 regions of 16S rRNA gene were amplified. The sequencing data was processed using the Quantitative Insights Into Microbial Ecology (QIIME version 1.9). The diversity, principal coordinate analysis (PCoA), nonmetric multidimensional scaling (NMDS), and linear discriminant analysis (LDA) effect size (LEfSe) were performed. Random-Forest classification was performed for discriminating the samples from different groups. Microbial function was assessed using the PICRUST. RESULTS: The Simpson in the control group was lower than that in the liver fibrosis group (p = 0.048) and differed significantly among different fibrosis stages (p = 0.047). The Chao1 index in the control group was higher than that in the liver fibrosis group (p < 0.001). NMDS analysis showed a marked difference between the control and liver fibrosis groups (p < 0.001). PCoA analysis indicated the different community composition between the control and liver fibrosis groups with variances of PC1 13.76% and PC2 5.89% and between different liver fibrosis stages with variances of PC1 10.51% and PC2 7.78%. LEfSe analysis showed alteration of gut microbiota in the liver fibrosis group. Biomarkers obtained from Random-Forest classification showed excellent diagnostic accuracy in prediction of liver fibrosis with AUROCs of 0.99. The AUROCs were 0.77~0.84 in prediction of stage F4. There were six increased and 17 decreased metabolic functions in the liver fibrosis group and 6 metabolic functions significantly differed among four liver fibrosis stages. CONCLUSION: Gut microbiota is a potential biomarker for detecting and staging liver fibrosis with high diagnostic accuracies.
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spelling pubmed-73225942020-07-17 Gut Microbiota and Liver Fibrosis: One Potential Biomarker for Predicting Liver Fibrosis Li, Zhiming Ni, Ming Yu, Haiyang Wang, Lili Zhou, Xiaoming Chen, Tao Liu, Guangzhen Gao, Yuanxiang Biomed Res Int Research Article PURPOSE: To investigate the relationship between gut microbiota and liver fibrosis and establish a microbiota biomarker for detecting and staging liver fibrosis. METHODS: 131 Wistar rats were used in our study, and liver fibrosis was induced by carbon tetrachloride. Stool samples were collected within 72 hours after the last administration. The V4 regions of 16S rRNA gene were amplified. The sequencing data was processed using the Quantitative Insights Into Microbial Ecology (QIIME version 1.9). The diversity, principal coordinate analysis (PCoA), nonmetric multidimensional scaling (NMDS), and linear discriminant analysis (LDA) effect size (LEfSe) were performed. Random-Forest classification was performed for discriminating the samples from different groups. Microbial function was assessed using the PICRUST. RESULTS: The Simpson in the control group was lower than that in the liver fibrosis group (p = 0.048) and differed significantly among different fibrosis stages (p = 0.047). The Chao1 index in the control group was higher than that in the liver fibrosis group (p < 0.001). NMDS analysis showed a marked difference between the control and liver fibrosis groups (p < 0.001). PCoA analysis indicated the different community composition between the control and liver fibrosis groups with variances of PC1 13.76% and PC2 5.89% and between different liver fibrosis stages with variances of PC1 10.51% and PC2 7.78%. LEfSe analysis showed alteration of gut microbiota in the liver fibrosis group. Biomarkers obtained from Random-Forest classification showed excellent diagnostic accuracy in prediction of liver fibrosis with AUROCs of 0.99. The AUROCs were 0.77~0.84 in prediction of stage F4. There were six increased and 17 decreased metabolic functions in the liver fibrosis group and 6 metabolic functions significantly differed among four liver fibrosis stages. CONCLUSION: Gut microbiota is a potential biomarker for detecting and staging liver fibrosis with high diagnostic accuracies. Hindawi 2020-06-19 /pmc/articles/PMC7322594/ /pubmed/32685479 http://dx.doi.org/10.1155/2020/3905130 Text en Copyright © 2020 Zhiming Li et al. http://creativecommons.org/licenses/by/4.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Li, Zhiming
Ni, Ming
Yu, Haiyang
Wang, Lili
Zhou, Xiaoming
Chen, Tao
Liu, Guangzhen
Gao, Yuanxiang
Gut Microbiota and Liver Fibrosis: One Potential Biomarker for Predicting Liver Fibrosis
title Gut Microbiota and Liver Fibrosis: One Potential Biomarker for Predicting Liver Fibrosis
title_full Gut Microbiota and Liver Fibrosis: One Potential Biomarker for Predicting Liver Fibrosis
title_fullStr Gut Microbiota and Liver Fibrosis: One Potential Biomarker for Predicting Liver Fibrosis
title_full_unstemmed Gut Microbiota and Liver Fibrosis: One Potential Biomarker for Predicting Liver Fibrosis
title_short Gut Microbiota and Liver Fibrosis: One Potential Biomarker for Predicting Liver Fibrosis
title_sort gut microbiota and liver fibrosis: one potential biomarker for predicting liver fibrosis
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7322594/
https://www.ncbi.nlm.nih.gov/pubmed/32685479
http://dx.doi.org/10.1155/2020/3905130
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