ArticleNPJ digital medicine2026
Cohort vs case-control design for transformer-based prediction of asthma exacerbations in mild asthma.
Article in NPJ digital medicine, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.
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.
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.
Who cites it
2 citing papers in PubMed.
- Article
- Asthma Burden in Mild Adult Asthma in the PEARL Survey: Asthma Control and Health Status.The journal of allergy and clinical immunology. In practice · 2026Article
Corrections and comments
PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.
Authors and funding
8 authors.
Funding
Abstract
Acute asthma exacerbation (AAE) is among the most serious outcomes of asthma, and accurate prediction of its risk remains a key challenge. Existing electronic health record-based prediction models have typically adopted either cohort or case-control sampling designs, yet their comparative performance has not been systematically evaluated. To address this gap, we developed transformer-based deep learning models to predict AAE among adults with mild asthma, directly comparing cohort and case-control designs using identical predictors and architecture across two large integrated healthcare systems, Kaiser Permanente Southern California (KPSC) and Kaiser Permanente Northwest (KPNW). Models were trained on retrospective data from KPSC and externally validated in KPNW. Mean area under the receiver operating characteristic curve (AUC) was 0.85 for case-control models and 0.70 (KPSC)/0.71 (KPNW) for cohort models. Both designs generalized well across systems, indicating robust feature learning and population transferability. Although calibration appeared well aligned within each analytical framework, absolute predicted probabilities diverged between designs, reflecting how event-enriched sampling inflates apparent risk and affects interpretability. These findings demonstrate that study design strongly influences model behavior and should be aligned with the intended use when developing predictive models for clinical deployment.
Identifiers
What OpenQuestion holds
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.