Cardiology Research, ISSN 1923-2829 print, 1923-2837 online, Open Access
Article copyright, the authors; Journal compilation copyright, Cardiol Res and Elmer Press Inc
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Review

Volume 17, Number 5, October 2026, pages 406-415


Prediction of Risk of Cardiovascular Events in Patients With Stable Angina Using Artificial Intelligence: A Systematic Review

Figure

↓  Figure 1. The PRISMA flow diagram for this systematic review. PRISMA: Preferred Reporting Items for Systematic Reviews and Meta-Analyses.
Figure 1.

Tables

↓  Table 1. Inclusion and Exclusion Criteria
 
CategoryInclusion criteriaExclusion criteria
MI: myocardial infarction; EHR: electronic health record; ECG: electrocardiogram; MACE: major adverse cardiovascular events.
PopulationAdult patients (≥ 18 years) diagnosed with stable angina or chronic coronary syndromePatients with acute coronary syndrome, unstable angina, post-MI only cohorts, pediatric populations
Intervention/exposureStudies applying artificial intelligence, machine learning, or deep learning modelsStudies using only traditional statistical risk scores without AI/ML components
OutcomesPrediction of cardiovascular events (e.g., MACE, MI, mortality, heart failure, stroke, revascularization)Studies not reporting cardiovascular outcomes or focused only on diagnostic accuracy without outcome prediction
Study designObservational studies (retrospective or prospective), cohort studies, registry-based studiesCase reports, editorials, letters, commentaries, conference abstracts, posters, dissertations
Data typeUse of clinical data, ECG, imaging, EHR, laboratory data, or multimodal datasetsAnimal studies, simulation-only studies, non-clinical datasets
Publication typePeer-reviewed journal articlesPreprints without peer review, short communications, reviews
Time framePublished within the last 10 yearsPublications which were prior to the specified time window
LanguageArticles published in EnglishNon-English publications

 

↓  Table 2. Summarized Literature for the Systematic Review
 
ReferenceTargetVariableArchitecturePre-processingDatasetSelection Criteria and OutcomeResult
ACS: acute coronary syndrome; AHA: American Heart Association; BMI: body mass index; CAD: coronary artery disease; CCTA: coronary computed tomography angiography; CHD: coronary heart disease; CI: confidence interval; CNN: convolutional neural network; CV: cardiovascular; CVE: cardiovascular events; D-F: Diamond–Forrester; DM: diabetes mellitus; ECG: electrocardiogram; EHR: electronic health records; ExtCAD: extensive coronary artery disease; FHx: family history; HF: heart failure; HTN: hypertension; MI: myocardial infarction; ObstCAD: obstructive coronary artery disease; QCG: quantitative electrocardiography; QC: quality control; UA: unstable angina; vars: variables; WHO: World Health Organization.
[17]AI-ECG detection of obstructive CAD in stable anginaAge, sex, BMI, symptom type, HTN, DM, dyslipidemia, smoking, stroke, FHx + QCG scores + ECG deep featuresResNet-CNN (16 layers, SE blocks, nonlocal); task layers (Adam + focal loss; temp scaling). XGBoost on extracted vectors (80/20; 5-fold CV)Signal extraction, feature vectors, probability calibration, CV for tuningSNUBH, 2018–2020, n = 723Outpatients with stable angina symptoms undergoing invasive angiography. Excluded: asymptomatic, prior CAD/revascularization, and emergency ACS cases.AUROC: 0.827
Outcome: any obstructive CAD
[18]Obstructive + extensive CAD in suspected stable anginaClinical risk factors + QCG scoresModified ResNet encoderPatient-level split (90/10), bootstrap CI (2000)SNUBH, 2011–2019, n = 21,866Outpatients evaluated via invasive angiography/CCTA for chest pain. External validation: independent multi-cohort sample. Excluded: emergency ACS admissions.AUC: ObstCAD 0.781; severe 0.780; ExtCAD 0.689
Outcome: obstructive CAD
[13]Obstructive CAD and assess prognosis in suspected stable anginaAge, sex, angina typicality, dyspnoa; risk factors (DM, dyslipidemia, FHx); Charlson indexStatistical models: logistic regression (basic + clinical); Cox regression for prognosisSymptom classification (typical/atypical/non-cardiac), D-F pre-test probability, registry linkage, 30-day blanking periodSingle-center, Denmark, n = 3,903Consecutive single-center outpatient referrals. Baseline status: verified free of baseline CAD and heart failure at entry.AUC: 0.88
Outcome: obstructive CAD
Composite outcome (death, MI, UA, HF, stroke)
[19]12-month CVE in stable angina + CHDPhysical activity, Antiplatelet use, Traditional Chinese medicine, Gensini score, SAQ Exertional capacity, SAQ Anginal stabilityML models: XGBoost, LightGBM, RF, AdaBoost, MLP, SVM, KNN, GNB) + logistic regression,Prospective cohort, random split 7:3, 10-fold CV, missing MICE imputation, SHAP for interpretabilitySingle-center, n = 827Prospective cohort with established WHO/AHA-defined stable coronary disease. Excluded: advanced systemic illness, heart failure, or cognitive barriers.AUC: train 1.00, validation 0.98, test 0.98 (95% CI 0.97–1.00)
Best = LightGBM; also kept multivariable logistic regression (nomogram + online calculator)
Outcome: composite CVE: nonfatal MI, revascularization, all-cause death, readmission (angina/HF/malignant arrhythmia), stroke
[20]ACS risk in stable CHDEHR vars → QC → 34 clinical vars (labs + diagnoses + utilization + sociodemographics)T2G-Former + MLP: build feature-relation graph → transformer embeddings → MLP outputs ACS baselines: CatBoost, LightGBM, XGBoost, RF, SVM, FT-TransformerConvert heterogeneous variables, imputation, patient-level longitudinal mean, MICE (checked vs k-NN), multicollinearity check 5-fold stratified CV, repeated across 12 seedsRaw: 268,876 CHD records from 165 institutions, n = 12,336Outpatients with stable angina symptoms undergoing invasive angiography.The F1 scores were 0.666, 0.757, and 0.886 at 6, 12, and 24 months, respectively.
Outcome: progression from stable CHD → ACS within 6/12/24 months