A Hybrid Risk Assessment Model for Cardiovascular Disease Using Cox Regression Analysis and a 2-means clustering

T Vivekanandan1, Swathi Jamjala Narayanan2

  • 1School of Computing Science and Engineering, VIT University, Vellore, 632014, Tamil Nadu, India; Department of Computer Science and Engineering, SITAMS, Chittoor, 517127, Andhra Pradesh, India.

Insights

This study introduces a hybrid model for cardiovascular disease (CVD) risk assessment, improving prediction accuracy by identifying critical factors. The model effectively predicts individual CVD risk, offering a valuable tool for early detection and prevention.

Area of Science:

  • Biomedical Engineering
  • Data Science
  • Cardiology

Background:

  • Cardiovascular disease (CVD) poses a significant threat, with current prediction methods for presence or absence being insufficient.
  • Accurate assessment of individual CVD risk, including likelihood of cardiac events, is crucial for effective management.
  • Identifying and analyzing controllable and uncontrollable factors contributing to CVD is complex and time-consuming.

Purpose of the Study:

  • To develop and evaluate a hybrid model for precise individual cardiovascular disease risk assessment.
  • To optimize the identification of critical factors influencing CVD using a modified Differential Evolution (DE) algorithm.
  • To predict cumulative prevalence ratios and determine individual CVD risk using Cox regression and 2-means clustering.

Main Methods:

  • Feature optimization using a modified Differential Evolution (DE) algorithm to identify critical CVD-related attributes.
  • Cox regression analysis to evaluate prevalence rates of critical attributes and predict cumulative prevalence ratios.
  • 2-means clustering technique applied to cumulative prevalence ratios for individual CVD risk stratification.

Main Results:

  • The hybrid model achieved 91% prediction accuracy for cardiovascular disease using optimized critical attributes via Cox regression.
  • The 2-means clustering demonstrated effective risk stratification, with Davies-Bouldin (DB) indices of 0.282 (CVD group) and 0.2836 (non-CVD group).
  • The model's performance, particularly the Cox regression accuracy, surpassed other existing models.

Conclusions:

  • The developed hybrid model offers a robust and accurate method for individual cardiovascular disease risk assessment.
  • The integration of optimized feature selection, Cox regression, and 2-means clustering provides a powerful approach to CVD risk stratification.
  • This approach enhances the ability to predict and manage cardiovascular disease risk more effectively.

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