Evidence map›Paper›PMID 40749856›Full record

Trial reportGastroenterology2026

Low Fermentable Oligosaccharides, Disaccharides, Monosaccharides, and Polyols Diet Improves Colonic Barrier Function and Mast Cell Activation in Patients With Diarrhea-Predominant Irritable Bowel Syndrome: A Mechanistic Trial.

Jun Gao, Allen A Lee, Shabnam Abtahi, Jerrold R Turner, Madhusudan Grover, Alexander Schmidt, Thomas M Schmidt, Judy W Nee, Johanna Iturrino, Anthony Lembo and 3 more

Erratum issued Registry-linked trialAbstract readClinical TrialMulticenter Study
In one paragraph

Trial report in Gastroenterology, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. An erratum has been issued. It is linked to trial NCT04542018 (Effects of Low FODMAP Diet on Colonic Epithelial Physiology in Diarrhea-predominant Irritable Bowel Syndrome), which is not on this map. Cited by 8 papers, 2 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
8citing papers in PubMed, 2 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.

NCT04542018 nacompletednot on this map

Effects of Low FODMAP Diet on Colonic Epithelial Physiology in Diarrhea-predominant Irritable Bowel Syndrome

TypeinterventionalSponsorUniversity of MichiganRan2020 to 2024Enrolled48ConditionsIrritable Bowel SyndromeArmsa low FODMAP diet for 4 weeks
3 · Its place in the literature

Who cites it

8 citing papers in PubMed, 2 syntheses or guidelines pooled it.

  1. Pooled it
  2. Pooled it
  3. Article
  4. Letter: Low-FODMAP Diet in Irritable Bowel Syndrome-Beyond the Hype!Alimentary pharmacology & therapeutics · 2026
    Article
  5. Critical Review: The Past, Present, and Future of Small Intestinal Bacterial Overgrowth (SIBO).JGH open : an open access journal of gastroenterology and hepatology · 2026
    Review
  6. Irritable bowel syndrome with diarrhea: time to change practice?Current opinion in gastroenterology · 2026
    Review
  7. Review
  8. MicroencapsulatedFrontiers in cellular and infection microbiology · 2026
    Article
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

13 authors.

Jun GaoDivision of Gastroenterology, Department of Internal Medicine, Michigan Medicine, Ann Arbor, Michigan.
Allen A LeeDivision of Gastroenterology, Department of Internal Medicine, Michigan Medicine, Ann Arbor, Michigan.
Shabnam AbtahiLaboratory of Mucosal Barrier Pathobiology, Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Jerrold R TurnerLaboratory of Mucosal Barrier Pathobiology, Department of Pathology, Brigham and Women's Hospital and Harvard Medical School, Boston, Massachusetts.
Madhusudan GroverDivision of Gastroenterology and Hepatology, Enteric Neuroscience Program, Mayo Clinic, Rochester, Minnesota.
Alexander SchmidtDepartment of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan.
Thomas M SchmidtDepartment of Microbiology and Immunology, University of Michigan, Ann Arbor, Michigan; Department of Ecology and Evolutionary Biology, University of Michigan, Ann Arbor, Michigan; Department of Internal Medicine, Division of Infectious Diseases, University of Michigan, Ann Arbor, Michigan.
Judy W NeeDivision of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Johanna IturrinoDivision of Gastroenterology, Beth Israel Deaconess Medical Center, Boston, Massachusetts.
Anthony LemboDigestive Disease and Surgery Institute, Cleveland Clinic, Cleveland, Ohio.
William D CheyDivision of Gastroenterology, Department of Internal Medicine, Michigan Medicine, Ann Arbor, Michigan.
John W WileyDivision of Gastroenterology, Department of Internal Medicine, Michigan Medicine, Ann Arbor, Michigan.
Prashant SinghDivision of Gastroenterology, Department of Internal Medicine, Michigan Medicine, Ann Arbor, Michigan. Electronic address: Singhpr@med.umich.edu.

Funding

ZO-1-MEDIATED PROTEIN INTERACTIONS: REGULATORS AND INTEGRATORS OF DIVERSE EPITHELIAL FUNCTIONS IN HEALTH AND DISEASER01DK061931 · NIDDK · UNIVERSITY OF CHICAGO · PI JERROLD R. TURNER · 2001 to 2026
$15.0M
Therapeutic targeting of protein interactions to reverse MLCK1-mediated intestinal barrier loss and ameliorate disease.R01DK068271 · NIDDK · UNIVERSITY OF CHICAGO · PI JERROLD R. TURNER · 2005 to 2026
$11.3M
NIDDK NIH HHS R01 DK061931NIDDK NIH HHS R01 DK068271
6 · The paper itself

Abstract

BACKGROUND &

aimsA diet low in fermentable oligosaccharides, disaccharides, monosaccharides, and polyols (LFD) is the most efficacious dietary therapy for irritable bowel syndrome (IBS). However, the mechanisms by which fermentable oligosaccharides, disaccharides, monosaccharides, and polyols drive IBS pathophysiology are unclear.

methodsPatients with Rome IV diarrhea-predominant IBS (IBS-D) underwent barrier function evaluation pre- and post-LFD along with assessment of mast cell number and activation profile. Finally, fecal supernatants (FS) were administered intracolonically to wild-type mice with and without pharmacologic inhibition, toll-like receptor 4 (tlr4)

resultsOf 42 patients, 34 responded to the LFD and 8 did not. Patients with IBS-D had significant improvement in colonic barrier structure and function, mast cell number, and levels of mast cell mediators post-LFD. The magnitude of physiological changes did not correlate with the magnitude of clinical response. Humanization of germ-free mice with pre-LFD feces caused barrier dysfunction and post-LFD feces did not. Similarly, pre-LFD FS caused barrier dysfunction in wild-type mice, whereas post-LFD FS did not. Lipopolysaccharide removal and TLR4 antagonism reversed pre-LFD IBS FS-induced barrier dysfunction. Barrier dysfunction was absent in tlr4

conclusionsPatients with IBS-D exhibited improvement in colonic barrier dysfunction, mast cell recruitment, and activation post LFD. Fermentable oligosaccharides, disaccharides, monosaccharides, and polyols-mediated barrier dysfunction in IBS-D is mediated by direct activation of the TLR4 receptor on colonic mast cells by fecal lipopolysaccharide. CLINICALTRIALS: gov, Number: NCT04542018.

Indexed as

ColonDiarrheaDiet, Carbohydrate-RestrictedIrritable Bowel SyndromeMast CellsOligosaccharidesAdultAnimalsDisaccharidesDisease Models, AnimalFecesFemaleFermentationHumansIntestinal MucosaMaleDisaccharidesMonosaccharidesOligosaccharidesPolymerspolyolTLR4 protein, humanTlr4 protein, mouseToll-Like Receptor 4Immune CellsIntestinal PermeabilityMicrobiomePathophysiology

Identifiers

PMID40749856
PMCPMC13123426

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Registered trials

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.