Evidence mapPaperPMID 41917007Full record

ArticleNature communications2026

Small intestinal microbial fiber metabolism dysfunction in celiac disease.

Mark Wulczynski, Marco Constante, Heather J Galipeau, JedidJah Blom, Gaston H Rueda, Nancy El-Chaar, Dorothy K Superdock, Sharon Jiang, Lawrence A David, Joseph A Murray and 6 more

Abstract read
In one paragraph

Article in Nature communications, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing papers in PubMed
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

4 citing papers in PubMed.

  1. Gut microbes · 2026
    Article
  2. Article
  3. Article
  4. Review
4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

16 authors.

Mark WulczynskiFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.
Marco ConstanteFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.
Heather J GalipeauFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.
JedidJah BlomFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.
Gaston H RuedaFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.
Nancy El-ChaarFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.ORCID 0009-0002-2573-9509
Dorothy K SuperdockDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0001-5348-3307
Sharon JiangDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC, USA.
Lawrence A DavidDepartment of Molecular Genetics and Microbiology, Duke University School of Medicine, Durham, NC, USA.ORCID 0000-0002-3570-4767
Joseph A MurrayDivision of Gastroenterology and Hepatology, Mayo Clinic, Rochester, MN, USA.
Michael G SuretteFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.ORCID 0000-0003-0086-4995
David ArmstrongFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.ORCID 0000-0003-2487-1479
Maria Ines Pinto-SanchezFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.
Premysl BercikFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada.ORCID 0000-0001-8707-1781
Alberto CamineroFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada. Acamine@mcmaster.ca.ORCID 0000-0001-9555-7167
Elena F VerduFarncombe Family Digestive Health Research Institute - McMaster University, Hamilton, ON, Canada. Verdue@mcmaster.ca.ORCID 0000-0001-6346-2665

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Celiac disease (CeD) is an immune-mediated condition driven by dietary gluten resulting in small intestinal mucosal inflammation and injury, along with myriads of symptoms. The only treatment is a lifelong gluten-free diet (GFD) and although most patients improve, the restriction can lead to nutrient deficiencies including fiber. Duodenal microbiota is known to be altered in CeD, but whether and how the microbial fiber metabolism may be affected is unknown. Here we show that CeD patients had impaired microbial fiber metabolism in the small intestine which associated with depletion of the fiber degrading taxa, Prevotella spp, independent of treatment with the GFD. Colonization of germ-free mice with Prevotella spp increased small intestinal short chain fatty acids (SCFA). In gluten-sensitized mice expressing the celiac risk gene, HLA-DQ8, an inulin-supplemented diet facilitated microbial saccharolytic function and SCFA production to accelerate mucosal healing in the small intestine during the GFD. The results support clinical investigations of dietary fiber supplementation and microbial fiber degradation to enhance responses to the GFD in CeD.

Indexed as

Celiac DiseaseDietary FiberGastrointestinal MicrobiomeIntestine, SmallAnimalsDiet, Gluten-FreeDuodenumFatty Acids, VolatileFemaleGlutensHLA-DQ AntigensHumansIntestinal MucosaInulinMaleMiceDietary FiberFatty Acids, VolatileGlutensHLA-DQ8 antigenHLA-DQ AntigensInulin

Identifiers

PMID41917007
PMCPMC13039995

What Socratic holds

Textmetadata
LicenceCC BY-NC-ND
Read underepoch 390

Registered trials

None linked

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 Socratic graph.