Evidence map›Paper›PMID 40938864›Full record

ArticlePloS one2025

An interpretable LightGBM model for predicting coronary heart disease: Enhancing clinical decision-making with machine learning.

Lang Deng, Kongjie Lu, Huanhuan Hu

Abstract read
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Article in PloS one, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

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0cells of the map it votes in
4citing 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

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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

4 citing papers in PubMed.

  1. [Development and validation of a machine learning-based prediction model for fatty liver in Wilson disease].Nan fang yi ke da xue xue bao = Journal of Southern Medical University · 2026
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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

3 authors.

Lang DengHuzhou Central Hospital, Fifth School of Clinical Medicine of Zhejiang Chinese Medical University, Huzhou, China.ORCID 0000-0003-3558-7836
Kongjie LuHuzhou Central Hospital, Fifth School of Clinical Medicine of Zhejiang Chinese Medical University, Huzhou, China.
Huanhuan HuHuzhou Central Hospital, Fifth School of Clinical Medicine of Zhejiang Chinese Medical University, Huzhou, China.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

backgroundCoronary Heart Disease (CHD) is one of the major burdens of cardiovascular diseases worldwide. Traditional diagnostic methods, such as coronary angiography and electrocardiogram, face challenges including high costs, subjectivity, and high misdiagnosis rates. To address these issues, this study proposes a prediction framework for CHD based on the LightGBM algorithm, aiming to improve the accuracy and interpretability of CHD risk prediction.

methodsThis study utilized three publicly available datasets: BRFSS_2015, Framingham, and Z-Alizadeh Sani. The BRFSS_2015 dataset was used for model training, while the Framingham and Z-Alizadeh Sani datasets were employed for validation. Data preprocessing included cleaning, feature engineering, and handling missing values. The LightGBM model was selected for its efficiency and performance, and SHAP (SHapley Additive exPlanations) values were used to enhance model interpretability. Model performance was evaluated using metrics such as accuracy, precision, recall, F1-score, and AUROC. A CHD scoring system was developed based on the model's predictions to assist clinicians in risk assessment.

resultsThe LightGBM model demonstrated excellent performance, achieving an accuracy of 90.60% and an AUROC of 81.06% on the BRFSS_2015 dataset. After parameter tuning, the model's accuracy improved to 90.61%, and the AUROC increased to 81.11%. On the Framingham dataset, the accuracy improved from 83.96% to 85.26%, and the AUROC increased from 62.86% to 67.37%. On the Z-Alizadeh Sani dataset, the accuracy improved from 78.69% to 80.33%, and the precision increased from 74.40% to 76.36%.

conclusionsSHAP analysis revealed that age, smoking status, diabetes, hypertension, and high cholesterol were the most influential features in predicting CHD risk. The developed CHD scoring system provided a user-friendly tool for clinicians to assess patient risk levels effectively.

Indexed as

Clinical Decision-MakingCoronary DiseaseMachine LearningAgedAlgorithmsBoosting Machine Learning AlgorithmsFemaleHumansMaleMiddle AgedRisk Assessment

Identifiers

PMID40938864
PMCPMC12431356

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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.