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Human Gut Microbiota Changes Reveal the Progression of Glucose Intolerance
To explore the relationship of gut microbiota with the development of type 2 diabetes (T2DM), we analyzed 121 subjects who were divided into 3 groups based on their glucose intolerance status: normal glucose tolerance (NGT; n = 44), prediabetes (Pre-DM; n = 64), or newly diagnosed T2DM (n = 13). Gut...
Autores principales: | , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Public Library of Science
2013
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3754967/ https://www.ncbi.nlm.nih.gov/pubmed/24013136 http://dx.doi.org/10.1371/journal.pone.0071108 |
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author | Zhang, Xiuying Shen, Dongqian Fang, Zhiwei Jie, Zhuye Qiu, Xinmin Zhang, Chunfang Chen, Yingli Ji, Linong |
author_facet | Zhang, Xiuying Shen, Dongqian Fang, Zhiwei Jie, Zhuye Qiu, Xinmin Zhang, Chunfang Chen, Yingli Ji, Linong |
author_sort | Zhang, Xiuying |
collection | PubMed |
description | To explore the relationship of gut microbiota with the development of type 2 diabetes (T2DM), we analyzed 121 subjects who were divided into 3 groups based on their glucose intolerance status: normal glucose tolerance (NGT; n = 44), prediabetes (Pre-DM; n = 64), or newly diagnosed T2DM (n = 13). Gut microbiota characterizations were determined with 16S rDNA-based high-throughput sequencing. T2DM-related dysbiosis was observed, including the separation of microbial communities and a change of alpha diversity between the different glucose intolerance statuses. To assess the correlation between metabolic parameters and microbiota diversity, clinical characteristics were also measured and a significant association between metabolic parameters (FPG, CRP) and gut microbiota was found. In addition, a total of 28 operational taxonomic units (OTUs) were found to be related to T2DM status by the Kruskal-Wallis H test, most of which were enriched in the T2DM group. Butyrate-producing bacteria (e.g. Akkermansia muciniphila ATCCBAA-835, and Faecalibacterium prausnitzii L2-6) had a higher abundance in the NGT group than in the pre-DM group. At genus level, the abundance of Bacteroides in the T2DM group was only half that of the NGT and Pre-DM groups. Previously reported T2DM-related markers were also compared with the data in this study, and some inconsistencies were noted. We found that Verrucomicrobiae may be a potential marker of T2DM as it had a significantly lower abundance in both the pre-DM and T2DM groups. In conclusion, this research provides further evidence of the structural modulation of gut microbiota in the pathogenesis of diabetes. |
format | Online Article Text |
id | pubmed-3754967 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2013 |
publisher | Public Library of Science |
record_format | MEDLINE/PubMed |
spelling | pubmed-37549672013-09-06 Human Gut Microbiota Changes Reveal the Progression of Glucose Intolerance Zhang, Xiuying Shen, Dongqian Fang, Zhiwei Jie, Zhuye Qiu, Xinmin Zhang, Chunfang Chen, Yingli Ji, Linong PLoS One Research Article To explore the relationship of gut microbiota with the development of type 2 diabetes (T2DM), we analyzed 121 subjects who were divided into 3 groups based on their glucose intolerance status: normal glucose tolerance (NGT; n = 44), prediabetes (Pre-DM; n = 64), or newly diagnosed T2DM (n = 13). Gut microbiota characterizations were determined with 16S rDNA-based high-throughput sequencing. T2DM-related dysbiosis was observed, including the separation of microbial communities and a change of alpha diversity between the different glucose intolerance statuses. To assess the correlation between metabolic parameters and microbiota diversity, clinical characteristics were also measured and a significant association between metabolic parameters (FPG, CRP) and gut microbiota was found. In addition, a total of 28 operational taxonomic units (OTUs) were found to be related to T2DM status by the Kruskal-Wallis H test, most of which were enriched in the T2DM group. Butyrate-producing bacteria (e.g. Akkermansia muciniphila ATCCBAA-835, and Faecalibacterium prausnitzii L2-6) had a higher abundance in the NGT group than in the pre-DM group. At genus level, the abundance of Bacteroides in the T2DM group was only half that of the NGT and Pre-DM groups. Previously reported T2DM-related markers were also compared with the data in this study, and some inconsistencies were noted. We found that Verrucomicrobiae may be a potential marker of T2DM as it had a significantly lower abundance in both the pre-DM and T2DM groups. In conclusion, this research provides further evidence of the structural modulation of gut microbiota in the pathogenesis of diabetes. Public Library of Science 2013-08-27 /pmc/articles/PMC3754967/ /pubmed/24013136 http://dx.doi.org/10.1371/journal.pone.0071108 Text en © 2013 Zhang et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited. |
spellingShingle | Research Article Zhang, Xiuying Shen, Dongqian Fang, Zhiwei Jie, Zhuye Qiu, Xinmin Zhang, Chunfang Chen, Yingli Ji, Linong Human Gut Microbiota Changes Reveal the Progression of Glucose Intolerance |
title | Human Gut Microbiota Changes Reveal the Progression of Glucose Intolerance |
title_full | Human Gut Microbiota Changes Reveal the Progression of Glucose Intolerance |
title_fullStr | Human Gut Microbiota Changes Reveal the Progression of Glucose Intolerance |
title_full_unstemmed | Human Gut Microbiota Changes Reveal the Progression of Glucose Intolerance |
title_short | Human Gut Microbiota Changes Reveal the Progression of Glucose Intolerance |
title_sort | human gut microbiota changes reveal the progression of glucose intolerance |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3754967/ https://www.ncbi.nlm.nih.gov/pubmed/24013136 http://dx.doi.org/10.1371/journal.pone.0071108 |
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