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Impaired Gut-Liver-Brain Axis in Patients with Cirrhosis

Cirrhosis is associated with brain dysfunction known as hepatic encephalopathy (HE). The mechanisms behind HE are unclear although hyperammonemia and systemic inflammation through gut dysbiosis have been proposed. We aimed to define the individual contribution of specific gut bacterial taxa towards...

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Autores principales: Ahluwalia, Vishwadeep, Betrapally, Naga S, Hylemon, Phillip B, White, Melanie B, Gillevet, Patrick M, Unser, Ariel B, Fagan, Andrew, Daita, Kalyani, Heuman, Douglas M, Zhou, Huiping, Sikaroodi, Masoumeh, Bajaj, Jasmohan S
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Nature Publishing Group 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880966/
https://www.ncbi.nlm.nih.gov/pubmed/27225869
http://dx.doi.org/10.1038/srep26800
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author Ahluwalia, Vishwadeep
Betrapally, Naga S
Hylemon, Phillip B
White, Melanie B
Gillevet, Patrick M
Unser, Ariel B
Fagan, Andrew
Daita, Kalyani
Heuman, Douglas M
Zhou, Huiping
Sikaroodi, Masoumeh
Bajaj, Jasmohan S
author_facet Ahluwalia, Vishwadeep
Betrapally, Naga S
Hylemon, Phillip B
White, Melanie B
Gillevet, Patrick M
Unser, Ariel B
Fagan, Andrew
Daita, Kalyani
Heuman, Douglas M
Zhou, Huiping
Sikaroodi, Masoumeh
Bajaj, Jasmohan S
author_sort Ahluwalia, Vishwadeep
collection PubMed
description Cirrhosis is associated with brain dysfunction known as hepatic encephalopathy (HE). The mechanisms behind HE are unclear although hyperammonemia and systemic inflammation through gut dysbiosis have been proposed. We aimed to define the individual contribution of specific gut bacterial taxa towards astrocytic and neuronal changes in brain function using multi-modal MRI in patients with cirrhosis. 187 subjects (40 controls, 147 cirrhotic; 87 with HE) underwent systemic inflammatory assessment, cognitive testing, stool microbiota analysis and brain MRI analysis. MR spectroscopy (MRS) changes of increased Glutamate/glutamine, reduced myo-inositol and choline are hyperammonemia-associated astrocytic changes, while diffusion tensor imaging (DTI) demonstrates changes in neuronal integrity and edema. Linkages between cognition, MRI parameters and gut microbiota were compared between groups. We found that HE patients had a significantly worse cognitive performance, systemic inflammation, dysbiosis and hyperammonemia compared to controls and cirrhotics without HE. Specific microbial families (autochthonous taxa negatively and Enterobacteriaceae positively) correlated with MR spectroscopy and hyperammonemia-associated astrocytic changes. On the other hand Porphyromonadaceae, were only correlated with neuronal changes on DTI without linkages with ammonia. We conclude that specific gut microbial taxa are related to neuronal and astrocytic consequences of cirrhosis-associated brain dysfunction.
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spelling pubmed-48809662016-06-08 Impaired Gut-Liver-Brain Axis in Patients with Cirrhosis Ahluwalia, Vishwadeep Betrapally, Naga S Hylemon, Phillip B White, Melanie B Gillevet, Patrick M Unser, Ariel B Fagan, Andrew Daita, Kalyani Heuman, Douglas M Zhou, Huiping Sikaroodi, Masoumeh Bajaj, Jasmohan S Sci Rep Article Cirrhosis is associated with brain dysfunction known as hepatic encephalopathy (HE). The mechanisms behind HE are unclear although hyperammonemia and systemic inflammation through gut dysbiosis have been proposed. We aimed to define the individual contribution of specific gut bacterial taxa towards astrocytic and neuronal changes in brain function using multi-modal MRI in patients with cirrhosis. 187 subjects (40 controls, 147 cirrhotic; 87 with HE) underwent systemic inflammatory assessment, cognitive testing, stool microbiota analysis and brain MRI analysis. MR spectroscopy (MRS) changes of increased Glutamate/glutamine, reduced myo-inositol and choline are hyperammonemia-associated astrocytic changes, while diffusion tensor imaging (DTI) demonstrates changes in neuronal integrity and edema. Linkages between cognition, MRI parameters and gut microbiota were compared between groups. We found that HE patients had a significantly worse cognitive performance, systemic inflammation, dysbiosis and hyperammonemia compared to controls and cirrhotics without HE. Specific microbial families (autochthonous taxa negatively and Enterobacteriaceae positively) correlated with MR spectroscopy and hyperammonemia-associated astrocytic changes. On the other hand Porphyromonadaceae, were only correlated with neuronal changes on DTI without linkages with ammonia. We conclude that specific gut microbial taxa are related to neuronal and astrocytic consequences of cirrhosis-associated brain dysfunction. Nature Publishing Group 2016-05-26 /pmc/articles/PMC4880966/ /pubmed/27225869 http://dx.doi.org/10.1038/srep26800 Text en Copyright © 2016, Macmillan Publishers Limited http://creativecommons.org/licenses/by/4.0/ This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/
spellingShingle Article
Ahluwalia, Vishwadeep
Betrapally, Naga S
Hylemon, Phillip B
White, Melanie B
Gillevet, Patrick M
Unser, Ariel B
Fagan, Andrew
Daita, Kalyani
Heuman, Douglas M
Zhou, Huiping
Sikaroodi, Masoumeh
Bajaj, Jasmohan S
Impaired Gut-Liver-Brain Axis in Patients with Cirrhosis
title Impaired Gut-Liver-Brain Axis in Patients with Cirrhosis
title_full Impaired Gut-Liver-Brain Axis in Patients with Cirrhosis
title_fullStr Impaired Gut-Liver-Brain Axis in Patients with Cirrhosis
title_full_unstemmed Impaired Gut-Liver-Brain Axis in Patients with Cirrhosis
title_short Impaired Gut-Liver-Brain Axis in Patients with Cirrhosis
title_sort impaired gut-liver-brain axis in patients with cirrhosis
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4880966/
https://www.ncbi.nlm.nih.gov/pubmed/27225869
http://dx.doi.org/10.1038/srep26800
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