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Record W4410488951 · doi:10.1016/j.bneo.2025.100118

Replication of a GWAS signal near HLA-DQA2 with AML using a disease-only cohort and external population-based controls

2025· article· en· W4410488951 on OpenAlexafffund
Rose Laflamme, Véronique Lisi, Josée Hébert, Guy Sauvageau, Sébastien Lemieux, Vincent‐Philippe Lavallée, Guillaume Lettre

Bibliographic record

VenueBlood Neoplasia · 2025
Typearticle
Languageen
FieldImmunology and Microbiology
TopicT-cell and B-cell Immunology
Canadian institutionsInstitute for Research in Immunology and CancerCentre Hospitalier Universitaire Sainte-JustineHôpital Maisonneuve-RosemontUniversité de MontréalMontreal Heart Institute
FundersFondation Charles-BruneauFondation Institut de Cardiologie de MontréalCentre hospitalier universitaire Sainte-JustineCanada Research ChairsFonds de Recherche du Québec - SantéCole FoundationMinistère de l'Économie, de l’Innovation et des Exportations du QuébecGénome QuébecCanadian Institutes of Health ResearchAlliance de recherche numérique du CanadaGenome Canada
KeywordsReplication (statistics)Human leukocyte antigenCohortGenome-wide association studyPopulationDiseaseMedicineBiologyImmunologyGeneticsVirologyInternal medicineEnvironmental healthGeneSingle-nucleotide polymorphismAntigen

Abstract

fetched live from OpenAlex

ABSTRACT Acute myeloid leukemia (AML) is the most common type of acute leukemia in adults. Genome-wide association studies (GWAS) have identified four common inherited variants associated with AML risk, but these findings have not yet been confirmed in many independent datasets. Here, we performed a replication study with 567 AML cases from the Leucegene cohort and 1,865 controls from the population-based cohort CARTaGENE (CaG). Because genotypes were generated using different technologies in the two datasets (e.g. low- vs. high-coverage whole-genome sequencing), we applied stringent quality-control filters to minimize type I errors. We showed using data reduction methods (e.g. principal component analysis [PCA] and uniform manifold approximation and projection [UMAP]) that our approach successfully integrated the Leucegene and CaG genetic data. We replicated the association between cytogenetically normal (CN)-AML and rs3916765, a variant located near HLA-DQA2 (odds ratio [95% confidence interval] = 1.96 [1.26-3.06], P-value=0.003). The effect size of this association was stronger when we restricted the analyses to AML patients with NPM1 mutations (odds ratios >2.25). We also found that rs3916765 is a whole-blood expression quantitative trait locus (eQTL) for HLA-DOB (P-value=1.05x10 -14 ) and HLA-DQA2 (P-value=2.23x10 -4 ). Our results confirm that a common genetic variant at the HLA locus associates with AML risk and the expression of HLA class II genes, providing new opportunities to improve disease prognosis and treatment.

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 distilled prediction

Teacher imitation

Not calibrated prevalence, not ground truth. Human validation pending. Learned from the 10,348 direct Codex labels and 10,348 direct Gemma labels. Candidate is the union of thresholded teacher heads; consensus is their intersection. These outputs are machine_predicted_unvalidated and are not human labels or direct frontier model labels.

metaresearch head score (Codex)0.000
metaresearch head score (Gemma)0.000
Version: codex-gemma-dda1882f352aValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Observational · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.351
Threshold uncertainty score0.656

Codex and Gemma teacher scores by category

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

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 head0.007
GPT teacher head0.225
Teacher spread0.218 · 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 teacher head, 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 routes2
Has abstractyes

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