Evidence map›Paper›PMID 39755324›Full record

ArticleJournal of biomedical informatics2025

DOME: Directional medical embedding vectors from Electronic Health Records.

Jun Wen, Hao Xue, Everett Rush, Vidul A Panickan, Tianrun Cai, Doudou Zhou, Yuk-Lam Ho, Lauren Costa, Edmon Begoli, Chuan Hong and 5 more

Abstract read
In one paragraph

Article in Journal of biomedical informatics, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 1 paper.

0numbers the graph read from it
0cells of the map it votes in
1citing 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.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

1 citing paper in PubMed.

  1. Article
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

15 authors.

Jun WenHarvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Boston, MA, USA.
Hao XueDepartment of Computational Biology, Cornell University, Ithaca, NY, USA.
Everett RushDepartment of Energy, Oak Ridge National Laboratory, Oak Ridge, TN, USA.
Vidul A PanickanHarvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Boston, MA, USA.
Tianrun CaiVA Boston Healthcare System, Boston, MA, USA; Brigham and Women's Hospital, Boston, MA, USA.
Doudou ZhouDepartment of Statistics and Data Science, National University of Singapore, Singapore.
Yuk-Lam HoVA Boston Healthcare System, Boston, MA, USA.
Lauren CostaVA Boston Healthcare System, Boston, MA, USA.
Edmon BegoliDepartment of Energy, Oak Ridge National Laboratory, Oak Ridge, TN, USA.
Chuan HongDuke University, Durham, NC, USA.
J Michael GazianoHarvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Boston, MA, USA; Brigham and Women's Hospital, Boston, MA, USA.
Kelly ChoHarvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Boston, MA, USA; Brigham and Women's Hospital, Boston, MA, USA.
Katherine P LiaoHarvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Boston, MA, USA; Brigham and Women's Hospital, Boston, MA, USA.
Junwei LuVA Boston Healthcare System, Boston, MA, USA; Harvard T.H. Chan School of Public Health, Boston, MA, USA. Electronic address: junweilu@hsph.harvard.edu.
Tianxi CaiHarvard Medical School, Boston, MA, USA; VA Boston Healthcare System, Boston, MA, USA; Harvard T.H. Chan School of Public Health, Boston, MA, USA. Electronic address: tcai@hsph.harvard.edu.

Funding

Project-001P50MH129699 · NIMH · MASSACHUSETTS GENERAL HOSPITAL · PI MATTHEW K NOCK, JORDAN W SMOLLER · 2023 to 2026
$16.6M
VERITY: Value and Evidence in Rheumatology using bioInformaTics, and advanced analYticsP30AR072577 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI Daniel Hal Solomon · 2017 to 2026
$9.8M
Unraveling the Complexities of Risk and Mechanism in CancerR35CA220523 · NCI · HARVARD UNIVERSITY D/B/A HARVARD SCHOOL OF PUBLIC HEALTH · PI QUACKENBUSH, JOHN · 2018 to 2024
$6.0M
Leveraging electronic health records to optimize treatment selection and response in multiple sclerosisR01NS098023 · NINDS · UNIVERSITY OF PITTSBURGH AT PITTSBURGH · PI Zongqi Xia · 2016 to 2026
$4.6M
Bridging clinical trial and real-world data via machine learning to advance rheumatoid arthritis treatment strategiesR01AR080193 · NIAMS · BRIGHAM AND WOMEN'S HOSPITAL · PI CAI, TIANXI, LIAO, KATHERINE PHOENIX · 2022 to 2025
$2.7M
NCI NIH HHS R35 CA220523NIAMS NIH HHS P30 AR072577NIAMS NIH HHS R01 AR080193NIMH NIH HHS P50 MH129699NINDS NIH HHS R01 NS098023
6 · The paper itself

Abstract

motivationThe increasing availability of Electronic Health Record (EHR) systems has created enormous potential for translational research. Recent developments in representation learning techniques have led to effective large-scale representations of EHR concepts along with knowledge graphs that empower downstream EHR studies. However, most existing methods require training with patient-level data, limiting their abilities to expand the training with multi-institutional EHR data. On the other hand, scalable approaches that only require summary-level data do not incorporate temporal dependencies between concepts.

methodsWe introduce a DirectiOnal Medical Embedding (DOME) algorithm to encode temporally directional relationships between medical concepts, using summary-level EHR data. Specifically, DOME first aggregates patient-level EHR data into an asymmetric co-occurrence matrix. Then it computes two Positive Pointwise Mutual Information (PPMI) matrices to correspondingly encode the pairwise prior and posterior dependencies between medical concepts. Following that, a joint matrix factorization is performed on the two PPMI matrices, which results in three vectors for each concept: a semantic embedding and two directional context embeddings. They collectively provide a comprehensive depiction of the temporal relationship between EHR concepts.

resultsWe highlight the advantages and translational potential of DOME through three sets of validation studies. First, DOME consistently improves existing direction-agnostic embedding vectors for disease risk prediction in several diseases, for example achieving a relative gain of 5.5% in the area under the receiver operating characteristic (AUROC) for lung cancer. Second, DOME excels in directional drug-disease relationship inference by successfully differentiating between drug side effects and indications, correspondingly achieving relative AUROC gain over the state-of-the-art methods by 10.8% and 6.6%. Finally, DOME effectively constructs directional knowledge graphs, which distinguish disease risk factors from comorbidities, thereby revealing disease progression trajectories. The source codes are provided at https://github.com/celehs/Directional-EHR-embedding.

Indexed as

AlgorithmsElectronic Health RecordsMedical InformaticsHumansDirectional medical embeddingDisease risk predictionDrug-disease relationshipElectronic Health Records

Identifiers

PMID39755324
PMCPMC12040072

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