Evidence map›Paper›PMID 42050589›Full record

ArticleBMC medical informatics and decision making2026

PhenoNMF: A novel multi-layer matrix factorization framework for age-stratified comprehensive phenotypic similarity analysis.

Yutong Dai, Wanzhe Xu, Yitao Yang, Weihang Zhang, Martin Loza, Kenta Nakai

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Article in BMC medical informatics and decision making, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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5 · Who and what money

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6 authors.

Yutong DaiDepartment of Computational Biology and Medical Science, The University of Tokyo, Kashiwa, Japan.
Wanzhe XuDepartment of Computational Biology and Medical Science, The University of Tokyo, Kashiwa, Japan.
Yitao YangDepartment of Computational Biology and Medical Science, The University of Tokyo, Kashiwa, Japan.
Weihang ZhangDepartment of Computational Biology and Medical Science, The University of Tokyo, Kashiwa, Japan.
Martin LozaThe Institute of Medical Science, The University of Tokyo, Tokyo, Japan.
Kenta NakaiDepartment of Computational Biology and Medical Science, The University of Tokyo, Kashiwa, Japan. knakai@ims.u-tokyo.ac.jp.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundElectronic health record (EHR) data enable deep phenotyping for risk prediction and treatment evaluation; however, many existing approaches lack interpretability and are difficult to interpret and validate. Methods that rely on a single modality and disregard age stratification may obscure differences across life stages and weaken model traceability and generalizability.

methodWe developed PhenoNMF, a multimodal EHR phenotyping framework based on joint nonnegative matrix factorization. PhenoNMF learns sparse multimodal patterns from diagnoses, laboratory tests, and medications using modality-specific sparsity penalties. By excluding age from the decomposition and reintroducing it through age-weighted contribution projections, PhenoNMF captures multimodal co-occurrence within each common pattern module and compares these patterns across age groups. Within each common pattern module (CPM), we define an Age Network Coupling Score (ANCS) to rank diagnosis, laboratory, and medication triads supported by both age-weighted contribution and cross-modality association evidence.

resultsIn a large critical-care cohort, PhenoNMF showed improved clustering stability and stronger cross-modal structure than multiple unsupervised baselines, yielding CPMs with coherent clinical themes across the lifespan. High-scoring triads prioritized by the ANCS highlighted age-specific multimodal patterns and were used to construct age-stratified survival analyses. These analyses revealed patient subgroups in which laboratory abnormalities modified drug-associated survival associations, summarized using hazard ratios and absolute risk differences.

conclusionPhenoNMF provides an interpretable framework for multimodal EHR phenotyping that separates phenotype learning from age effects and reconnects them through ANCS. By linking age-stratified CPMs and multimodal triads to outcome-based risk measures, the framework supports more precise characterization of patient subgroups and age-specific treatment and risk interactions. CLINICAL TRIAL NUMBER: Not applicable.

Indexed as

Electronic Health RecordsPhenotypeAge FactorsClustering AlgorithmsHumansComorbidity networkElectronic health records (EHRs)Multimodal phenotypingPrecision medicineTreatment effect heterogeneity

Identifiers

PMID42050589
PMCPMC13267728

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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.