Evidence map›Paper›PMID 40954286›Full record

ArticleNature metabolism2025

Dietary fibre-adapted gut microbiome clears dietary fructose and reverses hepatic steatosis.

Sunhee Jung, Hosung Bae, Won-Suk Song, Yujin Chun, Johnny Le, Yasmine Alam, Amandine Verlande, Sung Kook Chun, Joohwan Kim, Miranda E Kelly and 10 more

Abstract read
In one paragraph

Article in Nature metabolism, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 16 papers, 1 of them a synthesis that pooled it.

0numbers the graph read from it
0cells of the map it votes in
16citing papers in PubMed, 1 pooled it
–field-weighted citation impact
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

16 citing papers in PubMed, 1 synthesis or guideline pooled it.

  1. Pooled it
  2. Review
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  5. Reframing obesity through the gut microbiota: functional dysbiosis and metabolic disease.Current opinion in clinical nutrition and metabolic care · 2026
    Review
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  10. Foods (Basel, Switzerland) · 2026
    Article
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4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

20 authors.

Sunhee Jung *Department of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Hosung Bae *Department of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.ORCID http://orcid.org/0000-0001-5848-7972
Won-Suk Song *Department of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Yujin ChunDepartment of Microbiology and Molecular Genetics, School of Medicine, University of California Irvine, Irvine, CA, USA.
Johnny LeDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Yasmine AlamDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Amandine VerlandeDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Sung Kook ChunDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.ORCID http://orcid.org/0000-0001-8207-0034
Joohwan KimDepartment of Microbiology and Molecular Genetics, School of Medicine, University of California Irvine, Irvine, CA, USA.
Miranda E KellyDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.ORCID http://orcid.org/0009-0003-2451-7207
Miranda L LopezDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Sang Hee ParkDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Daniel OnofreDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Jongwon BaekDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Ki-Hong JangDepartment of Microbiology and Molecular Genetics, School of Medicine, University of California Irvine, Irvine, CA, USA.
Varvara I RubtsovaDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Alexis AnicaDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.
Selma MasriDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA.ORCID http://orcid.org/0000-0002-8619-8331
Gina LeeDepartment of Microbiology and Molecular Genetics, School of Medicine, University of California Irvine, Irvine, CA, USA.
Cholsoon JangDepartment of Biological Chemistry, School of Medicine, University of California Irvine, Irvine, CA, USA. choljang@uci.edu.ORCID http://orcid.org/0000-0001-6651-4213

Funding

Univ.of Calif., Irvine Cancer Center Support GrantP30CA062203 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Melanie Funes · 1994 to 2026
$57.9M
MEDICAL SCIENTIST TRAINING PROGRAMT32GM008620 · NIGMS · UNIVERSITY OF CALIFORNIA-IRVINE · PI GOLDIN, ALAN L · 1999 to 2023
$8.1M
Circadian Clock and Myc-dependent Regulation of Cellular TransformationR01CA259370 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Selma Masri · 2022 to 2026
$3.0M
Circadian Clock Disruption and Colorectal CancerR01CA244519 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI Selma Masri · 2020 to 2026
$3.0M
Elucidating dietary fructose and alcohol interactions during liver cancer developmentR01AA029124 · NIAAA · UNIVERSITY OF CALIFORNIA-IRVINE · PI JANG, CHOLSOON · 2021 to 2025
$2.0M
Elucidating the regulation of RNA methylation by mTOR signaling in cancerK22CA234399 · NCI · UNIVERSITY OF CALIFORNIA-IRVINE · PI LEE, GINA · 2022 to 2023
$440k
Elucidating alcohol-induced metabolic remodeling of critical organsR21AA030358 · NIAAA · UNIVERSITY OF CALIFORNIA-IRVINE · PI JANG, CHOLSOON, SELDIN, MARCUS MICHAEL · 2023 to 2023
$412k
Elucidating the role of nonessential amino acid metabolism in diabetic skin woundsF31DK134173 · NIDDK · UNIVERSITY OF CALIFORNIA-IRVINE · PI Johnny Le · 2023 to 2026
$197k
American Diabetes Association (ADA) 11-23-PDF-03Ministry of Health and Welfare (Ministry of Health, Welfare and Family Affairs) HI19C1352National Research Foundation of Korea (NRF) 021R1A6A3A14039132National Research Foundation of Korea (NRF) 2021R1A6A3A-14039681National Research Foundation of Korea (NRF) RS-2024-00411784NCI NIH HHS K22 CA234399NCI NIH HHS P30 CA062203NCI NIH HHS R01 CA244519NCI NIH HHS R01 CA259370NIAAA NIH HHS R01 AA029124NIAAA NIH HHS R21 AA030358NIDDK NIH HHS F31 DK134173NIGMS NIH HHS T32 GM008620UC | UC Irvine | Chao Family Comprehensive Cancer Center (CFCCC) P30CA062203U.S. Department of Health & Human Services | National Institutes of Health (NIH) F31DK134173U.S. Department of Health & Human Services | National Institutes of Health (NIH) K22-CA234399U.S. Department of Health & Human Services | National Institutes of Health (NIH) R01-AA029124U.S. Department of Health & Human Services | National Institutes of Health (NIH) R21-AA030358U.S. Department of Health & Human Services | National Institutes of Health (NIH) T32GM008620U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01CA244519U.S. Department of Health & Human Services | NIH | National Cancer Institute (NCI) R01CA259370
6 · The paper itself

Abstract

Excessive consumption of the simple sugar fructose, which induces excessive hepatic lipogenesis and gut dysbiosis, is a risk factor for cardiometabolic diseases. Here we show in male mice that the gut microbiome, when adapted to dietary fibre inulin, catabolizes dietary fructose and mitigates or reverses insulin resistance, hepatic steatosis and fibrosis. Specifically, inulin supplementation, without affecting the host's small intestinal fructose catabolism, promotes the small intestinal microbiome to break down incoming fructose, thereby decreasing hepatic lipogenesis and fructose spillover to the colonic microbiome. Inulin also activates hepatic de novo serine synthesis and cystine uptake, augmenting glutathione production and protecting the liver from fructose-induced lipid peroxidation. These multi-modal effects of inulin are transmittable by the gut microbiome, where Bacteroides acidifaciens acts as a key player. Thus, the gut microbiome, adapted to use inulin (a fructose polymer), efficiently catabolizes dietary monomeric fructose, thereby protecting the host. These findings provide a mechanism for how fibre can facilitate the gut microbiome to mitigate the host's exposure to harmful nutrients and disease progression.

Indexed as

Dietary FiberFatty LiverFructoseGastrointestinal MicrobiomeAnimalsInsulin ResistanceInulinLiverMaleMiceMice, Inbred C57BLDietary FiberFructoseInulin

Identifiers

PMID40954286
PMCPMC12460171

What OpenQuestion holds

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Registered trials

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.