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Gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease

Non-alcoholic fatty liver disease (NAFLD) is closely associated with type 2 diabetes mellitus (T2D), and these two metabolic diseases demonstrate bidirectional influences. The identification of microbiome profiles that are specific to liver injury or impaired glucose metabolism may assist understand...

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Detalles Bibliográficos
Autores principales: Si, Jiyeon, Lee, Giljae, You, Hyun Ju, Joo, Sae Kyung, Lee, Dong Hyeon, Ku, Bon Jeong, Park, Seoyeon, Kim, Won, Ko, GwangPyo
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Research Network of Computational and Structural Biotechnology 2021
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591343/
https://www.ncbi.nlm.nih.gov/pubmed/34849196
http://dx.doi.org/10.1016/j.csbj.2021.10.032
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author Si, Jiyeon
Lee, Giljae
You, Hyun Ju
Joo, Sae Kyung
Lee, Dong Hyeon
Ku, Bon Jeong
Park, Seoyeon
Kim, Won
Ko, GwangPyo
author_facet Si, Jiyeon
Lee, Giljae
You, Hyun Ju
Joo, Sae Kyung
Lee, Dong Hyeon
Ku, Bon Jeong
Park, Seoyeon
Kim, Won
Ko, GwangPyo
author_sort Si, Jiyeon
collection PubMed
description Non-alcoholic fatty liver disease (NAFLD) is closely associated with type 2 diabetes mellitus (T2D), and these two metabolic diseases demonstrate bidirectional influences. The identification of microbiome profiles that are specific to liver injury or impaired glucose metabolism may assist understanding of the role of the gut microbiota in the relationship between NAFLD and T2D. Here, we studied a biopsy-proven Asian NAFLD cohort (n = 329; 187 participants with NAFLD, 101 with NAFLD and T2D, and 41 with neither) and identified Enterobacter, Romboutsia, and Clostridium sensu stricto as the principal taxa associated with the severity of NAFLD and T2D, whereas Ruminococcus and Megamonas were specific to NAFLD. In particular, the taxa that were associated with both severe liver pathology and T2D were also significantly associated with markers of diabetes, such as fasting blood glucose and Hb1Ac. Enterotype analysis demonstrated that participants with NAFLD had a significantly higher proportion of Bacteroides and a lower proportion of Ruminococcus than a Korean healthy twin cohort (n = 756). However, T2D could not be clearly distinguished from NAFLD. Analysis of an independent T2D cohort (n = 185) permitted us to validate the T2D-specific bacterial signature identified in the NAFLD cohort. Functional inference analysis revealed that endotoxin biosynthesis pathways were significantly enriched in participants with NAFLD and T2D, compared with those with NAFLD alone. These findings may assist with the development of effective therapeutic approaches for metabolic diseases that are associated with specific bacterial signatures.
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spelling pubmed-85913432021-11-29 Gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease Si, Jiyeon Lee, Giljae You, Hyun Ju Joo, Sae Kyung Lee, Dong Hyeon Ku, Bon Jeong Park, Seoyeon Kim, Won Ko, GwangPyo Comput Struct Biotechnol J Research Article Non-alcoholic fatty liver disease (NAFLD) is closely associated with type 2 diabetes mellitus (T2D), and these two metabolic diseases demonstrate bidirectional influences. The identification of microbiome profiles that are specific to liver injury or impaired glucose metabolism may assist understanding of the role of the gut microbiota in the relationship between NAFLD and T2D. Here, we studied a biopsy-proven Asian NAFLD cohort (n = 329; 187 participants with NAFLD, 101 with NAFLD and T2D, and 41 with neither) and identified Enterobacter, Romboutsia, and Clostridium sensu stricto as the principal taxa associated with the severity of NAFLD and T2D, whereas Ruminococcus and Megamonas were specific to NAFLD. In particular, the taxa that were associated with both severe liver pathology and T2D were also significantly associated with markers of diabetes, such as fasting blood glucose and Hb1Ac. Enterotype analysis demonstrated that participants with NAFLD had a significantly higher proportion of Bacteroides and a lower proportion of Ruminococcus than a Korean healthy twin cohort (n = 756). However, T2D could not be clearly distinguished from NAFLD. Analysis of an independent T2D cohort (n = 185) permitted us to validate the T2D-specific bacterial signature identified in the NAFLD cohort. Functional inference analysis revealed that endotoxin biosynthesis pathways were significantly enriched in participants with NAFLD and T2D, compared with those with NAFLD alone. These findings may assist with the development of effective therapeutic approaches for metabolic diseases that are associated with specific bacterial signatures. Research Network of Computational and Structural Biotechnology 2021-10-28 /pmc/articles/PMC8591343/ /pubmed/34849196 http://dx.doi.org/10.1016/j.csbj.2021.10.032 Text en © 2021 The Authors https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Research Article
Si, Jiyeon
Lee, Giljae
You, Hyun Ju
Joo, Sae Kyung
Lee, Dong Hyeon
Ku, Bon Jeong
Park, Seoyeon
Kim, Won
Ko, GwangPyo
Gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease
title Gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease
title_full Gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease
title_fullStr Gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease
title_full_unstemmed Gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease
title_short Gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease
title_sort gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC8591343/
https://www.ncbi.nlm.nih.gov/pubmed/34849196
http://dx.doi.org/10.1016/j.csbj.2021.10.032
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