Evidence map›Paper›PMID 41277578›Full record

ArticleClinical and translational science2025

Colonic Tissue Expression of MAdCAM-1 Is Not Predictive of Vedolizumab Responsiveness in Inflammatory Bowel Disease.

Nikhil Reddy, Jeremy A Klein, Nikita Thomas, Dejan Micic, Zifeng Deng, David T Rubin, Russell D Cohen, Sushila Dalal, Britt Christensen, Haider I Haider and 5 more

Abstract read
In one paragraph

Article in Clinical and translational science, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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

1 citing paper in PubMed.

  1. Article
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

15 authors.

Nikhil ReddyInflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.ORCID 0000-0002-2009-402X
Jeremy A KleinInflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.ORCID 0000-0001-5229-3413
Nikita ThomasInflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
Dejan MicicLoyola University Medical Center in the Division of Gastroenterology, Chicago, Illinois, USA.
Zifeng DengInflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
David T RubinInflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
Russell D CohenInflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
Sushila DalalInflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.
Britt ChristensenRoyal Melbourne Hospital, and University of Melbourne, Melbourne, Australia.
Haider I HaiderNew York Medical College (NYMC), Valhalla, New York, USA.
Vesta ValuckaiteBayer Pharmaceuticals, New Jersey, USA.
Katherine R MeckelUniversity of Chicago, Section of Gastroenterology, Chicago, Illinois, USA.
Marc BissonnetteUniversity of Chicago, Section of Gastroenterology, Chicago, Illinois, USA.
Christopher R WeberDepartment of Pathology, University of Chicago Medicine, Chicago, Illinois, USA.
Joel PekowInflammatory Bowel Disease Center, University of Chicago Medicine, Chicago, Illinois, USA.ORCID 0000-0002-4790-8994

Funding

Takeda International
6 · The paper itself

Abstract

We assessed the predictive value of MAdCAM-1 expression on response to vedolizumab in patients with inflammatory bowel disease. This was a retrospective, single-center, cohort study including 109 patients with pretreatment inflammation who completed at least three doses of vedolizumab. We described clinical and endoscopic outcomes of patients based on MAdCAM-1 expression. There was no significant difference in MAdCAM-1 expression when stratified by histology. Patients in clinical remission at 14 weeks had significantly lower median baseline MAdCAM-1 expression (37425.3 vs. 46278.9, p < 0.015). There was no difference in pretreatment MAdCAM-1 expression among patients who later achieved endoscopic or biologic response. In the posttreatment cohort, lower MAdCAM-1 expression was associated with an increased likelihood of endoscopic or biologic response (36719.5 vs. 44229.9, p < 0.038). However, posttreatment MAdCAM-1 expression did not significantly differ when stratified for clinical remission at 14 weeks. Ultimately, MAdCAM-1 immunohistochemistry has limited utility as a predictive biomarker but may provide insights into vedolizumab-associated bowel healing.

Indexed as

Antibodies, Monoclonal, HumanizedColonGastrointestinal AgentsInflammatory Bowel DiseasesMucoproteinsAdultAgedBiomarkersCell Adhesion MoleculesFemaleHumansImmunohistochemistryMaleMiddle AgedPredictive Value of TestsRemission InductionAntibodies, Monoclonal, HumanizedBiomarkersCell Adhesion MoleculesGastrointestinal AgentsMADCAM1 protein, humanMucoproteinsvedolizumabimmunologyinflammationmolecular therapeuticsmonoclonal antibodiespharmacologytherapeuticsgastrointestinal

Identifiers

PMID41277578
PMCPMC12641277

What OpenQuestion holds

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LicenceCC BY-NC-ND
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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 OpenQuestion graph.