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Record W4415157028 · doi:10.1186/s13023-025-03966-z

Feasibility of machine learning analysis for the identification of patients with possible primary ciliary dyskinesia

2025· article· en· W4415157028 on OpenAlexaff
Gully Burns, Carey Kauffman, Michele Manion, Ruth-Anne Langan Pai, Carlos Milla, Michael G. O’Connor, Adam J. Shapiro, Heidi Bjornson-Pennell

Bibliographic record

VenueOrphanet Journal of Rare Diseases · 2025
Typearticle
Languageen
FieldMedicine
TopicCystic Fibrosis Research Advances
Canadian institutionsMcGill University Health Centre
FundersNational Center for Advancing Translational SciencesNational Heart, Lung, and Blood InstituteNHLBI Division of Intramural ResearchNational Institutes of Health
KeywordsPrimary ciliary dyskinesiaIdentification (biology)DiseaseDyskinesiaHuman geneticsDiagnostic test

Abstract

fetched live from OpenAlex

BACKGROUND: Significant diagnostic delays are common in primary ciliary dyskinesia (PCD), a rare disease that is significantly underdiagnosed. Scalable screening methods could improve early identification and health outcomes. RESEARCH QUESTION: Can machine learning (ML) be used to screen for PCD in pediatric patients? STUDY DESIGN AND METHODS: We evaluated the feasibility of a random forest model to screen for PCD using data from the PCD Foundation Registry and a national claims database. We identified a cohort of pediatric patients (< 18 years of age) with diagnostic codes indicative of conditions potentially associated with PCD, and studied diagnostic, procedural, and pharmaceutical codes associated with PCD to develop ML features. Models were trained on composite claims data from confirmed patients with PCD, patients with Q34.8 (Specific Congenital Malformation of the Respiratory System) diagnosed within 6 months of an Electron Microscopy procedure (Q34.8 + EM), and a randomly-selected, matched control group. Model performance was tested through fivefold cross-validation. RESULTS: Using 82 confirmed pediatric PCD cases and 4161 matched controls, the model demonstrated variable performance (positive predictive value 0.45-0.73, sensitivity 0.75-0.94). Synthetic data augmentation did not improve results (positive predictive value 0.45-0.67, sensitivity 0.71-1.00). Expanding the dataset to include 319 Q34.8 + EM patients and 8214 controls improved performance (positive predictive value 0.51-0.54, sensitivity 0.82-0.90), suitable for screening. In a cohort of 1.32 million pediatric patients, 7705 were classified as positive, consistent with the estimated prevalence of PCD (1:7554). INTERPRETATION: This study demonstrates the feasibility of using ML to screen for PCD using claims data, even in the absence of a specific International Classification of Disease (ICD) code. While unvalidated, this work may serve as the basis for future ML efforts in rare disease detection. Such screening approaches may aid in the identification of individuals who may benefit from timely diagnostic testing and targeted interventions.

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)0.022
metaresearch head score (Gemma)0.039
Version: metacan-v3-hybrid-931329e0061cValidation status: machine_predicted_unvalidated
Candidate categoriesnone
Consensus categoriesnone
DomainCandidate signal: none · Consensus signal: none
Study designCandidate signal: Simulation or modeling · Consensus signal: none
GenreCandidate signal: Empirical · Consensus signal: Empirical
Teacher disagreement score0.022
Threshold uncertainty score0.114

Distilled classifier scores by category (both heads)

CategoryCodexGemma
Metaresearch0.0220.039
Meta-epidemiology (narrow)0.0010.000
Meta-epidemiology (broad)0.0010.002
Bibliometrics0.0020.001
Science and technology studies0.0000.001
Scholarly communication0.0010.001
Open science0.0010.001
Research integrity0.0010.001
Insufficient payload (model declined to judge)0.0010.001

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 head0.012
GPT teacher head0.301
Teacher spread0.289 · 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 designSimulation or modeling
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

Citations1
Published2025
Admission routes1
Has abstractyes

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