Evidence map›Paper›PMID 41640879›Full record

ArticleFrontiers in genetics2025

Coronary heart disease risk prediction based on GAIN imputation and interpretable machine learning.

Shulin Zhao, Baoyun Nan, Jun Guo, Wenkai Xu, Zhen Li

Abstract read
In one paragraph

Article in Frontiers in genetics, 2025. 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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1 · What the graph read from it

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2 · The registry

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Shulin ZhaoThe Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, China.
Baoyun NanThe Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, China.
Jun GuoThe Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, China.
Wenkai XuThe Quzhou Affiliated Hospital of Wenzhou Medical University, Quzhou People's Hospital, Quzhou, China.
Zhen LiSchool of Artificial Intelligence, Shenzhen University of Information Technology, Shenzhen, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Introduction: Coronary atherosclerotic heart disease (CHD) is a leading cause of morbidity and mortality worldwide, making timely identification critical for improving patient prognosis. However, traditional imaging examinations are limited by high costs and patient selection bias, while existing prediction models often lack interpretability and generalization ability. This study aimed to develop a robust, interpretable machine learning approach to address these challenges. Methods: This retrospective study analyzed hospitalized patients at Quzhou People's Hospital from July 2021 to March 2025. Patients diagnosed with CHD were categorized as positive samples, while those without cardiovascular disease served as negative controls. The dataset integrated demographic data, blood biomarkers, and vital signs. A Generative Adversarial Imputation Network (GAIN) was utilized to handle missing values, and multiple machine learning models were constructed and compared for prediction performance. Results: Among the evaluated algorithms, the XGBoost model achieved superior performance on the test set with an Area Under the Curve (AUC) of 0.9053. To enhance clinical utility, the integration of SHAP (SHapley Additive exPlanations) values enabled both global and local interpretation of model decisions. Key predictive factors identified included mean respiratory rate during hospitalization, age, high-sensitivity troponin I (hs-cTnI), and hypertension. Discussion: The developed model demonstrates robust prediction performance combined with high clinical interpretability. Unlike traditional "black box" models, this approach clarifies the contribution of specific risk factors. Crucially, the tool is well-suited for dual deployment: serving as an automated screening tool integrated into hospital electronic health records (EHRs) and as a self-monitoring aid for individuals with underlying health conditions via mobile health applications.

Indexed as

coronary heart diseasedisease predictionexplainable machine learningfeature fusionGAIN

Identifiers

PMID41640879
PMCPMC12867338

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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.