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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Autores principales: Jiyeon Si, Giljae Lee, Hyun Ju You, Sae Kyung Joo, Dong Hyeon Lee, Bon Jeong Ku, Seoyeon Park, Won Kim, GwangPyo Ko
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/7dc37f161f82414cabf7744c06602cd3
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spelling oai:doaj.org-article:7dc37f161f82414cabf7744c06602cd32021-11-10T04:23:02ZGut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease2001-037010.1016/j.csbj.2021.10.032https://doaj.org/article/7dc37f161f82414cabf7744c06602cd32021-01-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S2001037021004542https://doaj.org/toc/2001-0370Non-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.Jiyeon SiGiljae LeeHyun Ju YouSae Kyung JooDong Hyeon LeeBon Jeong KuSeoyeon ParkWon KimGwangPyo KoElsevierarticleType 2 diabetes mellitusNon-alcoholic fatty liver disease (NAFLD)Gut microbiomeBiomarkerEnterotypeBiotechnologyTP248.13-248.65ENComputational and Structural Biotechnology Journal, Vol 19, Iss , Pp 5920-5930 (2021)
institution DOAJ
collection DOAJ
language EN
topic Type 2 diabetes mellitus
Non-alcoholic fatty liver disease (NAFLD)
Gut microbiome
Biomarker
Enterotype
Biotechnology
TP248.13-248.65
spellingShingle Type 2 diabetes mellitus
Non-alcoholic fatty liver disease (NAFLD)
Gut microbiome
Biomarker
Enterotype
Biotechnology
TP248.13-248.65
Jiyeon Si
Giljae Lee
Hyun Ju You
Sae Kyung Joo
Dong Hyeon Lee
Bon Jeong Ku
Seoyeon Park
Won Kim
GwangPyo Ko
Gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease
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.
format article
author Jiyeon Si
Giljae Lee
Hyun Ju You
Sae Kyung Joo
Dong Hyeon Lee
Bon Jeong Ku
Seoyeon Park
Won Kim
GwangPyo Ko
author_facet Jiyeon Si
Giljae Lee
Hyun Ju You
Sae Kyung Joo
Dong Hyeon Lee
Bon Jeong Ku
Seoyeon Park
Won Kim
GwangPyo Ko
author_sort Jiyeon Si
title 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_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_sort gut microbiome signatures distinguish type 2 diabetes mellitus from non-alcoholic fatty liver disease
publisher Elsevier
publishDate 2021
url https://doaj.org/article/7dc37f161f82414cabf7744c06602cd3
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