Evidence map›Paper›PMID 40655132›Full record

ArticleTherapeutic advances in gastroenterology2025

Predicting resistance to biological therapy using human leukocyte antigen genes in patients with inflammatory bowel disease.

Ângela Domingues, Ana Carvalho, António Martinho, Caroline Soares, Diana Martins, Paula Sousa, Ricardo Araújo, Eugénia Cancela, Américo Silva, Paula Ministro

Registry-linked trialAbstract read
In one paragraph

Article in Therapeutic advances in gastroenterology, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. It is linked to trial NCT05040854 (Can we Rely on HLA to Predict Resistance to Biological Therapy in IBD Patients), which is not on this map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing 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.

NCT05040854 unknown statusnot on this map

Can we Rely on HLA to Predict Resistance to Biological Therapy in IBD Patients

TypeobservationalSponsorCentro Hospitalar Tondela-ViseuRan2021 to 2024Enrolled600ConditionsInflammatory Bowel DiseasesArmsHLA-DQA1*05 and DRB1
3 · Its place in the literature

Who cites it

2 citing papers in PubMed.

  1. Review
  2. Review
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

10 authors.

Ângela DominguesDepartment of Gastroenterology, ULS Viseu Dão Lafões, Avenida Rei Dom Duarte, Viseu 3504-509, Portugal.ORCID https://orcid.org/0000-0003-0731-1242
Ana CarvalhoDepartment of Gastroenterology, ULS Viseu Dão Lafões, Viseu, Portugal.
António MartinhoMolecular Genetics Laboratory, Coimbra Blood and Transplantation Center, Coimbra, Portugal.
Caroline SoaresDepartment of Gastroenterology, ULS Viseu Dão Lafões, Viseu, Portugal.ORCID https://orcid.org/0009-0005-2994-9054
Diana MartinsDepartment of Gastroenterology, ULS Viseu Dão Lafões, Viseu, Portugal.
Paula SousaDepartment of Gastroenterology, ULS Viseu Dão Lafões, Viseu, Portugal.
Ricardo AraújoDepartment of Gastroenterology, ULS Viseu Dão Lafões, Viseu, Portugal.
Eugénia CancelaDepartment of Gastroenterology, ULS Viseu Dão Lafões, Viseu, Portugal.
Américo SilvaDepartment of Gastroenterology, ULS Viseu Dão Lafões, Viseu, Portugal.
Paula MinistroDepartment of Gastroenterology, ULS Viseu Dão Lafões, Viseu, Portugal.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Background: The efficacy of anti-tumor necrosis factor (TNF) therapy in inflammatory bowel disease (IBD) is often compromised by the development of antidrug antibodies. In this setting, the human leukocyte antigen (HLA)-DQA1*05 allele has been significantly associated with the formation of antidrug antibodies to anti-TNF agents, loss of response, and treatment discontinuation. Objectives: We aimed to determine whether HLA-DQA1*05 genotyping is associated with clinically meaningful outcomes in patients with IBD. Design: A single-center, prospective study was conducted on patients with IBD who were naïve to biological treatment and were initiating therapy with anti-TNF agents, vedolizumab, or ustekinumab. Methods: All patients were genotyped for HLA-DQA1*05. The primary endpoint was the achievement of a composite outcome encompassing clinical, biochemical, and endoscopic remission at week 54, stratified by HLA-DQA1*05 status. The secondary endpoints included the evaluation of therapeutic persistence and the development of antidrug antibodies. Results: One hundred biologic-naïve patients with IBD initiating biological therapy were included in the study (72 on anti-TNF, 18 on vedolizumab, and 10 on ustekinumab); of these, 43% were HLA-DQA1*05 positive. The presence of the HLA-DQA1*05 allele was not associated with worse clinical outcomes, defined as the composite of clinical, biochemical, and endoscopic remission at week 54, in patients treated with anti-TNF agents, vedolizumab, or ustekinumab. In addition, no significant correlation was observed between the HLA-DQA1*05 genotype and reduced therapy persistence or increased immunogenicity. Conclusion: In our cohort of patients with IBD, the HLA-DQA1*05 genotype was not associated with a higher risk of treatment cessation or worse clinical outcomes. Trial registration: Can we rely on HLA to predict resistance to biological therapy in patients with IBD?URL: https://clinicaltrials.gov/study/NCT05040854?cond=Can%20we%20rely%20on%20HLA&rank=1. Registration number: NCT05040854 (clinicaltrials.gov).

Indexed as

biomarkersclinical trialsgenetics and molecular epidemiology

Identifiers

PMID40655132
PMCPMC12254679

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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.