Evidence map›Paper›PMID 40121395›Full record

ArticleBMC cardiovascular disorders2025

Optimizing heart disease diagnosis with advanced machine learning models: a comparison of predictive performance.

M Darshan Teja, G Mokesh Rayalu

Abstract readComparative Study
In one paragraph

Article in BMC cardiovascular disorders, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.

0numbers the graph read from it
0cells of the map it votes in
7citing 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

7 citing papers in PubMed.

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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

2 authors.

M Darshan TejaDepartment of Mathematics, School of Advanced Sciences, Vellore Institute of Technology, Vellore, India.
G Mokesh RayaluDepartment of Mathematics, School of Advanced Sciences, Vellore Institute of Technology, Vellore, India. mokesh.g@vit.ac.in.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Cardiovascular disease is the leading cause of mortality globally, necessitating precise and prompt predictive instruments to enhance patient outcomes. In recent years, machine learning methodologies have demonstrated significant potential in enhancing the precision and efficacy of health-related predictions, especially in the identification of heart disease. The dataset used in this study came from the UC Irvine Machine Learning Repository and included data from Cleveland, Switzerland, Hungary, Long Beach, and Statlog. We selected seven of the 1,190 cases, each with 12 attributes, for analysis. We used different machine learning models, like Random Forest, K-Nearest Neighbors, Logistic Regression, Naïve Bayes, Gradient Boosting, AdaBoost, XGBoost, and Bagged Trees, to check performance using accuracy, precision, recall, F1-score, and ROC-AUC. K-fold cross-validation (K = 10, K = 5) was conducted to guarantee the robustness and generalizability of these models. Random Forest exhibited remarkable stability, attaining 94% accuracy with K = 10 and 92% with K = 5, whereas XGBoost had a minor decrease during cross-validation (90% for K = 10, 89% for K = 5). KNN demonstrated possible overfitting, evidenced by a notable decline in accuracy (71% for K = 10, 72% for K = 5). XGBoost and Bagged Trees achieved the highest accuracy of 93%, followed by Random Forest and KNN at 91%. Furthermore, Random Forest and Bagged Trees exhibited the highest ROC-AUC values at 95%, and XGBoost demonstrated a ROC-AUC of 94%. The results demonstrate the effectiveness of ensemble methods in predicting cardiac diseases, along with the potential for future advancement through the incorporation of hybrid models and advanced survival analysis techniques.

Indexed as

Decision Support TechniquesDiagnosis, Computer-AssistedHeart DiseasesMachine LearningAgedDatabases, FactualFemaleHumansMaleMiddle AgedPredictive Value of TestsPrognosisReproducibility of ResultsRisk AssessmentConfusion matrixHeart diseasesMachine learning modelsMetricsROC-AUC

Identifiers

PMID40121395
PMCPMC11929227

What Socratic holds

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LicenceCC BY
Read underepoch 390

Registered trials

None linked

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 Socratic graph.