Metabolomics and microbial composition increase insight into the impact of dietary differences in cirrhosis.

Mediterranean diet Western diet cirrhosis fermented milk products gut microbial function metabolomics

Journal

Liver international : official journal of the International Association for the Study of the Liver
ISSN: 1478-3231
Titre abrégé: Liver Int
Pays: United States
ID NLM: 101160857

Informations de publication

Date de publication:
02 2020
Historique:
received: 09 07 2019
revised: 04 09 2019
accepted: 17 09 2019
pubmed: 24 9 2019
medline: 22 6 2021
entrez: 24 9 2019
Statut: ppublish

Résumé

Dietary changes can modulate gut microbiota and interact with cirrhosis. Our prior study demonstrated that microbial diversity was higher in cirrhotics from Turkish vs the USA, which was associated with lower risk of 90-day hospitalizations. We aimed to define gut microbial functional and metabolomic changes to increase insight into benefits of the Mediterranean compared to Western diets. In all, 139 Turkish (46 controls/50 compensated/43 decompensated) and 157 American subjects (48 controls/59 compensated/50 decompensated) were studied. Turkish subjects consumed a modified Mediterranean diet with daily fermented milk intake, whereas Americans consumed a Western diet. Predicted gut microbial functionalities and plasma metabolomics were compared between/within countries. Correlation network differences between microbiota and metabolites in cirrhotics from Turkey vs the USA were evaluated. Predicted microbial function showed lower amino acid, bioenergetics and lipid pathways, with functions related to vitamin B, glycan, xenobiotic metabolism, DNA/RNA synthesis, in cirrhotics from Turkey compared to the USA. Plasma metabolomics demonstrated higher relative lactate levels in Turkey vs the USA. The metabolite changes in decompensated cirrhosis, compared to controls, showed similar trends in Turkey and the USA, with reduced lipids and phosphocholines. Phosphocholines were significantly lower in patients hospitalized in 90 days (P = .03). Correlation networks in cirrhotics demonstrated linkage differences between beneficial taxa, Blautia and Oscillispira, and lactate and unsaturated lipids, in Turkey compared to American patients. A modified Mediterranean diet was associated with altered plasma metabolomics and beneficially alters microbiota functionality and correlations compared to Western diet in cirrhosis. These altered diet-microbial interactions could potentially affect the 90-day hospitalization risk.

Sections du résumé

BACKGROUND & AIMS
Dietary changes can modulate gut microbiota and interact with cirrhosis. Our prior study demonstrated that microbial diversity was higher in cirrhotics from Turkish vs the USA, which was associated with lower risk of 90-day hospitalizations. We aimed to define gut microbial functional and metabolomic changes to increase insight into benefits of the Mediterranean compared to Western diets.
METHODS
In all, 139 Turkish (46 controls/50 compensated/43 decompensated) and 157 American subjects (48 controls/59 compensated/50 decompensated) were studied. Turkish subjects consumed a modified Mediterranean diet with daily fermented milk intake, whereas Americans consumed a Western diet. Predicted gut microbial functionalities and plasma metabolomics were compared between/within countries. Correlation network differences between microbiota and metabolites in cirrhotics from Turkey vs the USA were evaluated.
RESULTS
Predicted microbial function showed lower amino acid, bioenergetics and lipid pathways, with functions related to vitamin B, glycan, xenobiotic metabolism, DNA/RNA synthesis, in cirrhotics from Turkey compared to the USA. Plasma metabolomics demonstrated higher relative lactate levels in Turkey vs the USA. The metabolite changes in decompensated cirrhosis, compared to controls, showed similar trends in Turkey and the USA, with reduced lipids and phosphocholines. Phosphocholines were significantly lower in patients hospitalized in 90 days (P = .03). Correlation networks in cirrhotics demonstrated linkage differences between beneficial taxa, Blautia and Oscillispira, and lactate and unsaturated lipids, in Turkey compared to American patients.
CONCLUSIONS
A modified Mediterranean diet was associated with altered plasma metabolomics and beneficially alters microbiota functionality and correlations compared to Western diet in cirrhosis. These altered diet-microbial interactions could potentially affect the 90-day hospitalization risk.

Identifiants

pubmed: 31544308
doi: 10.1111/liv.14256
pmc: PMC6980909
mid: NIHMS1051590
doi:

Types de publication

Journal Article Research Support, N.I.H., Extramural Research Support, Non-U.S. Gov't Research Support, U.S. Gov't, Non-P.H.S.

Langues

eng

Sous-ensembles de citation

IM

Pagination

416-427

Subventions

Organisme : Wellcome Trust
Pays : United Kingdom
Organisme : CSRD VA
ID : I01 CX001076
Pays : United States
Organisme : NCATS NIH HHS
ID : R21 TR002024
Pays : United States

Informations de copyright

© 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.

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Auteurs

I Jane Cox (IJ)

Institute for Hepatology London, Foundation for Liver Research, London, UK.
Faculty of Life Sciences & Medicine, King's College Hospital, London, UK.

Ramazan Idilman (R)

University of Ankara, Ankara, Turkey.

Andrew Fagan (A)

Virginia Commonwealth University and McGuire Veterans Affairs Medical Center, Richmond, VA, USA.

Dilara Turan (D)

University of Ankara, Ankara, Turkey.

Lola Ajayi (L)

Institute for Hepatology London, Foundation for Liver Research, London, UK.
Faculty of Life Sciences & Medicine, King's College Hospital, London, UK.

Adrien D Le Guennec (AD)

Randall Centre for Cell & Molecular Biophysics and Centre for Biomolecular Spectroscopy, King's College London, London, UK.

Simon D Taylor-Robinson (SD)

Department of Surgery and Cancer, Imperial College London, London, UK.

Fatih Karakaya (F)

University of Ankara, Ankara, Turkey.

Edith Gavis (E)

Virginia Commonwealth University and McGuire Veterans Affairs Medical Center, Richmond, VA, USA.

R Andrew Atkinson (R)

Randall Centre for Cell & Molecular Biophysics and Centre for Biomolecular Spectroscopy, King's College London, London, UK.

Roger Williams (R)

Institute for Hepatology London, Foundation for Liver Research, London, UK.
Faculty of Life Sciences & Medicine, King's College Hospital, London, UK.

Masoumeh Sikaroodi (M)

George Mason University, Manassas, VA, USA.

Shahzor Nizam (S)

George Mason University, Manassas, VA, USA.

Patrick M Gillevet (PM)

George Mason University, Manassas, VA, USA.

Jasmohan S Bajaj (JS)

Virginia Commonwealth University and McGuire Veterans Affairs Medical Center, Richmond, VA, USA.

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