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Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults

BACKGROUND: Recent evidence suggests that there is a link between metabolic diseases and bacterial populations in the gut. The aim of this study was to assess the differences between the composition of the intestinal microbiota in humans with type 2 diabetes and non-diabetic persons as control. METH...

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Autores principales: Larsen, Nadja, Vogensen, Finn K., van den Berg, Frans W. J., Nielsen, Dennis Sandris, Andreasen, Anne Sofie, Pedersen, Bente K., Al-Soud, Waleed Abu, Sørensen, Søren J., Hansen, Lars H., Jakobsen, Mogens
Formato: Texto
Lenguaje:English
Publicado: Public Library of Science 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816710/
https://www.ncbi.nlm.nih.gov/pubmed/20140211
http://dx.doi.org/10.1371/journal.pone.0009085
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author Larsen, Nadja
Vogensen, Finn K.
van den Berg, Frans W. J.
Nielsen, Dennis Sandris
Andreasen, Anne Sofie
Pedersen, Bente K.
Al-Soud, Waleed Abu
Sørensen, Søren J.
Hansen, Lars H.
Jakobsen, Mogens
author_facet Larsen, Nadja
Vogensen, Finn K.
van den Berg, Frans W. J.
Nielsen, Dennis Sandris
Andreasen, Anne Sofie
Pedersen, Bente K.
Al-Soud, Waleed Abu
Sørensen, Søren J.
Hansen, Lars H.
Jakobsen, Mogens
author_sort Larsen, Nadja
collection PubMed
description BACKGROUND: Recent evidence suggests that there is a link between metabolic diseases and bacterial populations in the gut. The aim of this study was to assess the differences between the composition of the intestinal microbiota in humans with type 2 diabetes and non-diabetic persons as control. METHODS AND FINDINGS: The study included 36 male adults with a broad range of age and body-mass indices (BMIs), among which 18 subjects were diagnosed with diabetes type 2. The fecal bacterial composition was investigated by real-time quantitative PCR (qPCR) and in a subgroup of subjects (N = 20) by tag-encoded amplicon pyrosequencing of the V4 region of the 16S rRNA gene. The proportions of phylum Firmicutes and class Clostridia were significantly reduced in the diabetic group compared to the control group (P = 0.03). Furthermore, the ratios of Bacteroidetes to Firmicutes as well as the ratios of Bacteroides-Prevotella group to C. coccoides-E. rectale group correlated positively and significantly with plasma glucose concentration (P = 0.04) but not with BMIs. Similarly, class Betaproteobacteria was highly enriched in diabetic compared to non-diabetic persons (P = 0.02) and positively correlated with plasma glucose (P = 0.04). CONCLUSIONS: The results of this study indicate that type 2 diabetes in humans is associated with compositional changes in intestinal microbiota. The level of glucose tolerance should be considered when linking microbiota with metabolic diseases such as obesity and developing strategies to control metabolic diseases by modifying the gut microbiota.
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spelling pubmed-28167102010-02-07 Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults Larsen, Nadja Vogensen, Finn K. van den Berg, Frans W. J. Nielsen, Dennis Sandris Andreasen, Anne Sofie Pedersen, Bente K. Al-Soud, Waleed Abu Sørensen, Søren J. Hansen, Lars H. Jakobsen, Mogens PLoS One Research Article BACKGROUND: Recent evidence suggests that there is a link between metabolic diseases and bacterial populations in the gut. The aim of this study was to assess the differences between the composition of the intestinal microbiota in humans with type 2 diabetes and non-diabetic persons as control. METHODS AND FINDINGS: The study included 36 male adults with a broad range of age and body-mass indices (BMIs), among which 18 subjects were diagnosed with diabetes type 2. The fecal bacterial composition was investigated by real-time quantitative PCR (qPCR) and in a subgroup of subjects (N = 20) by tag-encoded amplicon pyrosequencing of the V4 region of the 16S rRNA gene. The proportions of phylum Firmicutes and class Clostridia were significantly reduced in the diabetic group compared to the control group (P = 0.03). Furthermore, the ratios of Bacteroidetes to Firmicutes as well as the ratios of Bacteroides-Prevotella group to C. coccoides-E. rectale group correlated positively and significantly with plasma glucose concentration (P = 0.04) but not with BMIs. Similarly, class Betaproteobacteria was highly enriched in diabetic compared to non-diabetic persons (P = 0.02) and positively correlated with plasma glucose (P = 0.04). CONCLUSIONS: The results of this study indicate that type 2 diabetes in humans is associated with compositional changes in intestinal microbiota. The level of glucose tolerance should be considered when linking microbiota with metabolic diseases such as obesity and developing strategies to control metabolic diseases by modifying the gut microbiota. Public Library of Science 2010-02-05 /pmc/articles/PMC2816710/ /pubmed/20140211 http://dx.doi.org/10.1371/journal.pone.0009085 Text en Larsen 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
Larsen, Nadja
Vogensen, Finn K.
van den Berg, Frans W. J.
Nielsen, Dennis Sandris
Andreasen, Anne Sofie
Pedersen, Bente K.
Al-Soud, Waleed Abu
Sørensen, Søren J.
Hansen, Lars H.
Jakobsen, Mogens
Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults
title Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults
title_full Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults
title_fullStr Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults
title_full_unstemmed Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults
title_short Gut Microbiota in Human Adults with Type 2 Diabetes Differs from Non-Diabetic Adults
title_sort gut microbiota in human adults with type 2 diabetes differs from non-diabetic adults
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC2816710/
https://www.ncbi.nlm.nih.gov/pubmed/20140211
http://dx.doi.org/10.1371/journal.pone.0009085
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