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The role of microbiota in hepatic encephalopathy

Journal

GUT MICROBES
Volume 5, Issue 3, Pages 397-403

Publisher

TAYLOR & FRANCIS INC
DOI: 10.4161/gmic.28684

Keywords

covert hepatic encephalopathy; minimal hepatic encephalopathy; cirrhosis; rifaximin; lactulose; correlation network; dysbiosis; probiotic; endotoxin; systemic inflammation

Funding

  1. National Institute on Alcohol Abuse and Alcoholism [RO1AA020203]
  2. National Institute of Diabetes and Digestive and Kidney Diseases [RO1DK087913]

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Hepatic encephalopathy (HE), which consists of minimal (MHE) and overt (OHE) stages, is a model for impaired gut-liver-brain axis in cirrhosis. Microbiota changes in both stages have been associated with impaired cognition, endotoxemia, and inflammation. There is dysbiosis (reduced autochthonous taxa [Lachnospiraceae, Ruminococcaceae, and Clostridiales XIV] and increased Enterobacteriaceae and Streptococcaceae) with disease progression. In MHE, there is an increased abundance of Streptococcus salivarius linked to cognition and ammonia. In OHE, stool Alcaligenaceae and Porphyromonadaceae are associated with poor cognition. Colonic mucosal microbiome in cirrhosis is significantly different compared with stool and independently related to cognition. HE treatment can affect microbial composition and function; cognitive improvement in MHE after rifaximin, a non-absorbable antibiotic, occurred without significant stool microbiota composition change but improved metabolic linkages. Similarly, there are only modest lactulose and rifaximin-associated changes on microbiota composition in OHE. HE represents an important model to study microbiome-brain interactions.

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