MétaCan
Menu
← Back to cohort
Record W4407288127 · doi:10.1093/jcag/gwae059.218

A218 INFLAMMATORY PHENOTYPE AS A PREDICTOR OF TREATMENT RESPONSE IN ULCERATIVE COLITIS

2025· article· en· W4407288127 on OpenAlexaff
Abdullah Al-Darwish, Aze Wilson

Bibliographic record

VenueJournal of the Canadian Association of Gastroenterology · 2025
Typearticle
Languageen
FieldBiochemistry, Genetics and Molecular Biology
TopicInflammatory Bowel Disease
Canadian institutionsWestern University
Fundersnot available
KeywordsUlcerative colitisPhenotypeMedicineInternal medicineBiologyGeneticsDiseaseGene

Abstract

fetched live from OpenAlex

Abstract Background A variety of immune pathways contribute to the propagation of inflammation in ulcerative colitis (UC). Both, Th1- and Th2-associated cytokines and cells, have been implicated in the pathogenesis of the disease. Eosinophils, which are elicited by Th2 immune response, are increasingly recognized to have a pivotal role in the pathogenesis of UC, however, the exact link between eosinophils and UC disease outcomes and treatment responses over time is still incompletely defined. Aims We aim to evaluate the association between pre-treatment peripheral eosinophil counts and treatment response in patients with ulcerative colitis. Methods In this retrospective cohort study, data from 150 treatment naïve adult patients who were diagnosed with ulcerative colitis between 2005 and 2020 were reviewed. White blood count differential was collected at diagnosis and following exposure to one or more of the following treatments: corticosteroids, TNFa antagonists, or vedolizumab. Patients were stratified into two cohorts for analysis: “high-eosinophil” cohort (>=0.2x109cells/L) and “low-eosinophil” cohort (<0.2x109cells/L). The partial and endoscopic Mayo scores were evaluated at baseline and following treatment. Patients’ data were collected until their last gastroenterology follow-up or until surgical intervention. Demogoraphic data were summarized using descriptive statistics. Fisher’s Exact test was used to evaluate the association between eosinophil count and drug response as well as other outcomes. Results A total of 150 patients were included. 92 patients (63.3%) were included in the high-eosinophil cohort, while 58 patients (38.6%) were included in the low-eosinophil cohort. The median duration of follow-up was 78 months (IQR42.5) and 74 months (IQR45) in the high-eosinophil group and low-eosinophil group, respectively. Between the high-eosinophil group and low eosinophil group, there was no statistically significant difference in terms of steroid response (71.3%, 78.6% respectively, p=0.330), achieving steroid-free remission with TNFa antagonist (76%, 72.2% respectively, p=0.662), achieving steroid-free remission with vedolizumab (54.1%, 65.2% respectively, p=0.394), or disease refractoriness requiring more than 2 drug changes (15.4%, 8.8% respectively, p = 0.106). Conclusions This study did not show a correlation between baseline eosinophil count and response to therapy - corticosteroids, TNFa antagonist, and vedolizumab. Larger prospective studies are warranted to assess disease outcomes and treatment response to eosinophil-targeted therapy. Funding Agencies None

Fetched live from OpenAlex and de-inverted. Abstracts are not stored in this database: the inverted indexes are 8.6 GB of the frame’s 9.3 GB of text, and the host has 13 GB free.

How this classification was reachedexpand

Full frame machine prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. The Gemma side is a direct model label for every work in the frame, read from the title-only record. The Codex side is a classifier learned from the 10,348 direct Codex labels and calibrated to design-weighted sample rates; fields without enough sample support carry no Codex call. Candidate is the union of the two sides; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels.

metaresearch head score (Codex)0.001
metaresearch head score (Gemma)0.002
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: Observational
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.003
Threshold uncertainty score0.010

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0010.002
Meta-epidemiology (narrow)0.0000.000
Meta-epidemiology (broad)0.0000.000
Bibliometrics0.0010.001
Science and technology studies0.0000.000
Scholarly communication0.0000.000
Open science0.0000.000
Research integrity0.0000.000
Insufficient payload (model declined to judge)0.0030.000

Machine scores (provisional)

The two teacher heads of the student model, read on this work. A score orders the frame for review; it never asserts a category, and the validation status ships verbatim with every row.

Baseline scores from an immature model (maturity gate not passed, 7 training rounds). Scores rank; they never assert a category.

Opus teacher head0.004
GPT teacher head0.221
Teacher spread0.217 · how far apart the two teachers sit on this one work
Validation statusscore_only:v0-immature-baseline · verbatim from the scoring run: score_only means the number may rank works, and no category label ships from it

Classification

machine, unvalidated

Machine predicted; a candidate call from one source (direct Gemma or distilled Codex), not a consensus.

The models applied no category: nothing in the taxonomy fit this work.
Study designObservational
Domainnot available
GenreEmpirical

How this classification was reached, model by model and score by score, is at the end of the page under "How this classification was reached".

Quick stats

Citations0
Published2025
Admission routes1
Has abstractyes

Explore more

Same venueJournal of the Canadian Association of Gastroenterology→Same topicInflammatory Bowel Disease→French-language works237,207→