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ArticlePeer ReviewedOpen AccessPlagiarism Passed
Paper ID:IJSREM66021

Explainable AI for Early Disease Risk Prediction

Stream/Area:

-

Subject:

-

Paper ID:

IJSREM66021

Volume:

10 |

7 |

Jul 2026

Pages:

1-6

Publication Frequency:

Monthly (12 issues per year)

DOI
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Not assigned

License:International Journal of Scientific Research in Engineering and Management follows the Creative Commons Attribution 4.0 (CC BY 4.0) License, allowing free use and distribution with proper attribution.

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Authors

Santosh Kumar Panda

Santosh Kumar Panda

Department of Data Science

Symbiosis Skills And Professional University

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Abstract

Heart disease is the foremost cause of global mortality, claiming nearly 17.9 million lives every year. Early and accurate risk prediction using routine clinical data has the potential to fundamentally change this picture, yet most machine learning models proposed for this task remain locked behind algorithmic opacity that prevents physicians from trusting their predictions. This paper presents a complete, end-to-end Explainable AI (XAI) framework for heart disease risk prediction that couples strong classification performance with clinician-friendly interpretability. Working from a multi-source dataset of 1,190 patient records covering 11 clinical features, we perform thorough data cleaning — removing physiologically implausible cholesterol values and applying IQR-based outlier elimination — yielding 1020 analysis-ready records. Four classifiers are systematically trained and compared: LightGBM, XGBoost, Random Forest, and a soft-voting Voting Ensemble. Random Forest achieves the highest test accuracy of 0.9510 (AUC = 0.9812, Recall = 0.9583), with a confusion matrix showing only 6 false positives and 4 false negatives on 204 test samples. SHAP (SHapley Additive exPlanations) decomposition identifies ST slope, chest pain type, and exercise angina as the three dominant predictors, and generates per-patient waterfall explanations that clinicians can directly inspect alongside every prediction. The result is a framework where predictive accuracy and clinical transparency are achieved simultaneously.

KEYWORDS

Heart disease prediction explainable artificial intelligence SHAP gradient boosting LightGBM XGBoost Random Forest voting ensemble clinical decision support feature importance risk stratification.

Cite This Article

Santosh Kumar Panda, "Explainable AI for Early Disease Risk Prediction," International Journal of Scientific Research in Engineering and Management, vol. 10, no. 7, pp. 1-6, Jul 2026.

Full Article/Conclusion

This paper presented a complete, reproducible XAI pipeline for heart disease risk prediction, from raw data through cleaning, EDA, multi-model training, and SHAP-based interpretability. Four classifiers were evaluated on 1020 cleaned patient records: Random Forest achieved the best standalone accuracy of 0.9510 with AUC 0.9812 and recall 0.9583, verified by 5-fold CV (mean 0.9242 ± 0.0075). SHAP decomposition revealed that ST slope, chest pain type, and exercise angina dominate global predictions — in full agreement with established cardiology. Per-patient waterfall plots make individual predictions readable and challengeable by clinicians. The central finding of this work is that strong classification accuracy and genuine clinical transparency are not competing goals: with SHAP-augmented ensemble learning, both can be achieved simultaneously — and that combination is what will ultimately allow AI-powered risk screening to move from research publication into clinical practice.

References

[1]   G. A. Roth et al., "Global burden of cardiovascular diseases and risk factors, 1990–2019: Update from the GBD 2019 study," J. Am. Coll. Cardiol., vol. 76, no. 25, pp. 2982–3021, Dec. 2020. doi: 10.1016/j.jacc.2020.11.010 [2]   S. Mohan, C. Thirumalai, and G. Srivastava, "Effective heart disease prediction using hybrid machine learning techniques," IEEE Access, vol. 7, pp. 81542–81554, 2019. doi: 10.1109/ACCESS.2019.2923707 [3]   K. G. Nair and M. Soni, "Heart disease prediction using machine learning algorithms: A review," Int. J. Comput. Appl., vol. 180, no. 40, pp. 1–7, 2018. [4]   A. Holzinger, G. Langs, H. Denk, K. Zatloukal, and H. Müller, "Causability and explainability of artificial intelligence in medicine," WIREs Data Mining Knowl. Discov., vol. 9, no. 4, p. e1312, Jul. 2019. doi: 10.1002/widm.1312 [5]   S. M. Lundberg and S.-I. Lee, "A unified approach to interpreting model predictions," in Proc. 31st Conf. Neural Inf. Process. Syst. (NeurIPS), Long Beach, CA, USA, Dec. 2017, pp. 4765–4774. [6]   A. Javaid et al., "Explainability of machine learning-based cardiovascular risk prediction models: A systematic review," Front. Cardiovasc. Med., vol. 9, p. 884033, May 2022. doi: 10.3389/fcvm.2022.884033 [7]   T. Chen and C. Guestrin, "XGBoost: A scalable tree boosting system," in Proc. 22nd ACM SIGKDD Int. Conf. Knowledge Discovery and Data Mining, San Francisco, CA, USA, Aug. 2016, pp. 785–794. doi: 10.1145/2939672.2939785 [8]   L. Breiman, "Random forests," Mach. Learn., vol. 45, no. 1, pp. 5–32, Oct. 2001. doi: 10.1023/A:1010933404324 [9]   R. Detrano et al., "International application of a new probability algorithm for the diagnosis of coronary artery disease," Am. J. Cardiol., vol. 64, no. 5, pp. 304–310, Aug. 1989. doi: 10.1016/0002-9149(89)90524-9 [10]U. R. Acharya et al., "Application of deep convolutional neural network for automated detection of myocardial infarction using ECG signals," Inf. Sci., vol. 415–416, pp. 190–198, Nov. 2017. doi: 10.1016/j.ins.2017.06.027

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Publication Date

7/13/2026

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Double-Blind Peer Review

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