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Metabolic reprogramming of the intestinal microbiome with functional bile acid changes underlie the development of NAFLD.
Smirnova, Ekaterina; Muthiah, Mark D; Narayan, Nicole; Siddiqui, Mohamad S; Puri, Puneet; Luketic, Velimir A; Contos, Melissa J; Idowu, Michael; Chuang, Jen-Chieh; Billin, Andrew N; Huss, Ryan S; Myers, Robert P; Boyett, Sherry; Seneshaw, Mulugeta; Min, Hae-Ki; Mirshahi, Faridodin; Sanyal, Arun J.
Afiliação
  • Smirnova E; Department of BiostatisticsVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
  • Muthiah MD; Division of Gastroenterology and HepatologyNational University Health SystemSingapore.
  • Narayan N; Yong Loo Lin School of MedicineNational University of SingaporeSingapore.
  • Siddiqui MS; Second Genome Inc.South San FranciscoCaliforniaUSA.
  • Puri P; Division of Gastroenterology, Hepatology and NutritionDepartment of Internal MedicineVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
  • Luketic VA; Division of Gastroenterology, Hepatology and NutritionDepartment of Internal MedicineVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
  • Contos MJ; Division of Gastroenterology, Hepatology and NutritionDepartment of Internal MedicineVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
  • Idowu M; Department of PathologyVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
  • Chuang JC; Department of PathologyVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
  • Billin AN; Gilead Sciences Inc.Foster CityCaliforniaUSA.
  • Huss RS; Gilead Sciences Inc.Foster CityCaliforniaUSA.
  • Myers RP; Gilead Sciences Inc.Foster CityCaliforniaUSA.
  • Boyett S; Gilead Sciences Inc.Foster CityCaliforniaUSA.
  • Seneshaw M; Division of Gastroenterology, Hepatology and NutritionDepartment of Internal MedicineVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
  • Min HK; Division of Gastroenterology, Hepatology and NutritionDepartment of Internal MedicineVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
  • Mirshahi F; Division of Gastroenterology, Hepatology and NutritionDepartment of Internal MedicineVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
  • Sanyal AJ; Division of Gastroenterology, Hepatology and NutritionDepartment of Internal MedicineVirginia Commonwealth University School of MedicineRichmondVirginiaUSA.
Hepatology ; 76(6): 1811-1824, 2022 12.
Article em En | MEDLINE | ID: mdl-35561146
ABSTRACT
BACKGROUND AND

AIMS:

Bile acids are hepatic metabolites and have many properties considered to be relevant to the pathophysiology of NAFLD. Circulating levels of the intestinal microbiome-modified bile acid deoxycholate are increased in cirrhosis. APPROACH AND

RESULTS:

To further elucidate the role of bile acids and intestinal microbiota linked to bile acids in progressively severe NAFLD, a multiomic study of feces including 16S rRNA sequencing, microbial transcriptomics and metabolomics was performed in a cohort with varying phenotypes of NAFLD. Several bile acids of microbial origin derived from deoxycholic acid (DCA) (glycodeoxycholate, 7-ketodeoxycholic acid, dehydrocholic acid) increased with disease activity and fibrosis stage. These were linked to increased expression of microbial bile salt hydrolase, bile acid operon (BaiCD) and hydroxysteroid dehydrogenases (hdhA) required for DCA and downstream metabolite synthesis providing a mechanistic basis for altered bile acid profiles with disease progression. Bacteroidetes and several genera of Lachnospiraceae family containing DCA generating genes increased with increasing disease severity, whereas several potentially beneficial microbes sensitive to antibacterial effects of DCA e.g., Ruminococcaceae were decreased. The clinical relevance of these data was confirmed in an independent cohort enrolled in a clinical trial for NASH where at entry DCA and its conjugates were associated with advanced fibrosis. In patients treated with placebo, DCA declined in those with fibrosis regression and increased in those with fibrosis progression. DCA rose further in those with compensated cirrhosis when they experienced decompensation.

CONCLUSIONS:

These findings demonstrate a role for bile acids and the bile acid dependent microbiome in the development and progression of NAFLD and set the stage to leverage these findings for NASH biomarker development and for therapeutics.
Assuntos

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatopatia Gordurosa não Alcoólica / Microbioma Gastrointestinal Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Hepatology Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Hepatopatia Gordurosa não Alcoólica / Microbioma Gastrointestinal Tipo de estudo: Clinical_trials Limite: Humans Idioma: En Revista: Hepatology Ano de publicação: 2022 Tipo de documento: Article