Deep stool microbiome analysis in cirrhosis reveals an association between short-chain fatty acids and hepatic encephalopathy

Introduction and objectives: Hepatic encephalopathy (HE) is a complication of cirrhosis linked to the microbiome. We aimed to characterize the fecal microbiome of patients with prior and future overt HE, and explore the relationship between fecal species, short-chain fatty acids (SCFAs) and ammonia...

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Autores principales: Patricia P. Bloom, Jesús M. Luévano, Jr., Kelsey J. Miller, Raymond T. Chung
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Lenguaje:EN
Publicado: Elsevier 2021
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Acceso en línea:https://doaj.org/article/4630b5c3799a4dec8200a8e84dbd0e1c
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spelling oai:doaj.org-article:4630b5c3799a4dec8200a8e84dbd0e1c2021-11-18T04:45:59ZDeep stool microbiome analysis in cirrhosis reveals an association between short-chain fatty acids and hepatic encephalopathy1665-268110.1016/j.aohep.2021.100333https://doaj.org/article/4630b5c3799a4dec8200a8e84dbd0e1c2021-11-01T00:00:00Zhttp://www.sciencedirect.com/science/article/pii/S1665268121000326https://doaj.org/toc/1665-2681Introduction and objectives: Hepatic encephalopathy (HE) is a complication of cirrhosis linked to the microbiome. We aimed to characterize the fecal microbiome of patients with prior and future overt HE, and explore the relationship between fecal species, short-chain fatty acids (SCFAs) and ammonia on HE pathogenesis. Materials and methods: Consecutive inpatients and outpatients with cirrhosis were recruited. A single stool sample was collected and underwent shallow shotgun sequencing, and SCFA and ammonia quantification. Patients were followed until the end of the study period. Prior and new overt HE was diagnosed by the treating hepatologist. Results: Forty-nine patients with cirrhosis, mean MELD-Na 20 (SD = 9) and 33 (67%) with a history of OHE provided a stool sample. Over a median 85 days of follow up (interquartile range 34–181 days), 16 developed an OHE episode. Eight fecal bacterial species were associated with a history of OHE, and no species predicted future OHE. Bacterial species positively associated with SCFA content were inversely related to cirrhosis disease severity. Patients with a history of OHE had lower concentrations of 6 fecal SCFAs. Fecal ammonia concentrations were similar between those with and without a history of OHE (273 μmol/g ± 214 vs. 327 ± 234, P = 0.43). Conclusions: We found 8 fecal species and 6 SCFAs linked to OHE. Many of the species inversely linked to OHE also have an association with SCFA production. Further work is needed to detail this relationship and to develop targeted interventions to treat HE.Patricia P. BloomJesús M. Luévano, Jr.Kelsey J. MillerRaymond T. ChungElsevierarticleCirrhosisMicrobiomeEncephalopathyShort-chain fatty acidsAmmoniaSpecialties of internal medicineRC581-951ENAnnals of Hepatology, Vol 25, Iss , Pp 100333- (2021)
institution DOAJ
collection DOAJ
language EN
topic Cirrhosis
Microbiome
Encephalopathy
Short-chain fatty acids
Ammonia
Specialties of internal medicine
RC581-951
spellingShingle Cirrhosis
Microbiome
Encephalopathy
Short-chain fatty acids
Ammonia
Specialties of internal medicine
RC581-951
Patricia P. Bloom
Jesús M. Luévano, Jr.
Kelsey J. Miller
Raymond T. Chung
Deep stool microbiome analysis in cirrhosis reveals an association between short-chain fatty acids and hepatic encephalopathy
description Introduction and objectives: Hepatic encephalopathy (HE) is a complication of cirrhosis linked to the microbiome. We aimed to characterize the fecal microbiome of patients with prior and future overt HE, and explore the relationship between fecal species, short-chain fatty acids (SCFAs) and ammonia on HE pathogenesis. Materials and methods: Consecutive inpatients and outpatients with cirrhosis were recruited. A single stool sample was collected and underwent shallow shotgun sequencing, and SCFA and ammonia quantification. Patients were followed until the end of the study period. Prior and new overt HE was diagnosed by the treating hepatologist. Results: Forty-nine patients with cirrhosis, mean MELD-Na 20 (SD = 9) and 33 (67%) with a history of OHE provided a stool sample. Over a median 85 days of follow up (interquartile range 34–181 days), 16 developed an OHE episode. Eight fecal bacterial species were associated with a history of OHE, and no species predicted future OHE. Bacterial species positively associated with SCFA content were inversely related to cirrhosis disease severity. Patients with a history of OHE had lower concentrations of 6 fecal SCFAs. Fecal ammonia concentrations were similar between those with and without a history of OHE (273 μmol/g ± 214 vs. 327 ± 234, P = 0.43). Conclusions: We found 8 fecal species and 6 SCFAs linked to OHE. Many of the species inversely linked to OHE also have an association with SCFA production. Further work is needed to detail this relationship and to develop targeted interventions to treat HE.
format article
author Patricia P. Bloom
Jesús M. Luévano, Jr.
Kelsey J. Miller
Raymond T. Chung
author_facet Patricia P. Bloom
Jesús M. Luévano, Jr.
Kelsey J. Miller
Raymond T. Chung
author_sort Patricia P. Bloom
title Deep stool microbiome analysis in cirrhosis reveals an association between short-chain fatty acids and hepatic encephalopathy
title_short Deep stool microbiome analysis in cirrhosis reveals an association between short-chain fatty acids and hepatic encephalopathy
title_full Deep stool microbiome analysis in cirrhosis reveals an association between short-chain fatty acids and hepatic encephalopathy
title_fullStr Deep stool microbiome analysis in cirrhosis reveals an association between short-chain fatty acids and hepatic encephalopathy
title_full_unstemmed Deep stool microbiome analysis in cirrhosis reveals an association between short-chain fatty acids and hepatic encephalopathy
title_sort deep stool microbiome analysis in cirrhosis reveals an association between short-chain fatty acids and hepatic encephalopathy
publisher Elsevier
publishDate 2021
url https://doaj.org/article/4630b5c3799a4dec8200a8e84dbd0e1c
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AT kelseyjmiller deepstoolmicrobiomeanalysisincirrhosisrevealsanassociationbetweenshortchainfattyacidsandhepaticencephalopathy
AT raymondtchung deepstoolmicrobiomeanalysisincirrhosisrevealsanassociationbetweenshortchainfattyacidsandhepaticencephalopathy
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