Excess dietary fructose does not alter gut microbiota or permeability in humans: A pilot randomized controlled study.

Fecal microbiome excess dietary fructose fecal metabolome gut permeability non-alcoholic fatty liver disease

Journal

Journal of clinical and translational science
ISSN: 2059-8661
Titre abrégé: J Clin Transl Sci
Pays: England
ID NLM: 101689953

Informations de publication

Date de publication:
2021
Historique:
received: 21 02 2021
revised: 17 05 2021
accepted: 04 06 2021
entrez: 23 8 2021
pubmed: 24 8 2021
medline: 24 8 2021
Statut: epublish

Résumé

Non-alcoholic fatty liver disease (NAFLD) is an increasing cause of chronic liver disease that accompanies obesity and the metabolic syndrome. Excess fructose consumption can initiate or exacerbate NAFLD in part due to a consequence of impaired hepatic fructose metabolism. Preclinical data emphasized that fructose-induced altered gut microbiome, increased gut permeability, and endotoxemia play an important role in NAFLD, but human studies are sparse. The present study aimed to determine if two weeks of excess fructose consumption significantly alters gut microbiota or permeability in humans. We performed a pilot double-blind, cross-over, metabolic unit study in 10 subjects with obesity (body mass index [BMI] 30-40 mg/kg/m Routine blood, uric acid, liver function, and lipid measurements were unaffected by the fructose intervention. The fecal microbiome (including In contrast to rodent preclinical findings, excess fructose did not cause changes in the gut microbiome, metabolome, and permeability as well as endotoxemia in humans with obesity fed fructose for 14 days in amounts known to enhance NAFLD.

Identifiants

pubmed: 34422323
doi: 10.1017/cts.2021.801
pii: S2059866121008013
pmc: PMC8358846
doi:

Types de publication

Journal Article

Langues

eng

Pagination

e143

Subventions

Organisme : NIDDK NIH HHS
ID : K08 DK117064
Pays : United States

Informations de copyright

© The Association for Clinical and Translational Science 2021.

Déclaration de conflit d'intérêts

The authors have no conflicts of interest to declare.

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Auteurs

José O Alemán (JO)

Laboratory of Biochemical Genetics and Metabolism, Rockefeller University, New York, NY, USA.
New York University Langone Health Metabolomics Core Resource Laboratory, New York, NY, USA.

Wendy A Henderson (WA)

Institute for Collaboration on Health, Intervention and Policy, University of Connecticut, Storrs, CT, USA.

Jeanne M Walker (JM)

Clinical Research, The Rockefeller University Hospital, New York, NY, USA.

Andrea Ronning (A)

Bionutrition, The Rockefeller University Hospital, New York, NY, USA.

Drew R Jones (DR)

New York University Langone Health Metabolomics Core Resource Laboratory, New York, NY, USA.

Peter J Walter (PJ)

NIDDK Clinical Mass Spectrometry Core, National Institutes of Health, Bethesda, MD, USA.

Scott G Daniel (SG)

PennCHOP Microbiome Program, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Kyle Bittinger (K)

PennCHOP Microbiome Program, Children's Hospital of Philadelphia, Philadelphia, PA, USA.

Roger Vaughan (R)

Biostatistics, The Rockefeller University, New York, NY, USA.

Robert MacArthur (R)

Research Pharmacy, The Rockefeller University Hospital, New York, NY, USA.

Kun Chen (K)

Institute for Collaboration on Health, Intervention and Policy, University of Connecticut, Storrs, CT, USA.

Jan L Breslow (JL)

Laboratory of Biochemical Genetics and Metabolism, Rockefeller University, New York, NY, USA.

Peter R Holt (PR)

Laboratory of Biochemical Genetics and Metabolism, Rockefeller University, New York, NY, USA.

Classifications MeSH