Prognostic Modelling Studies of Coronary Heart Disease-A Systematic Review of Conventional and Genetic Risk Factor

Nayla Nasr1,2, Beáta Soltész3, János Sándor2

  • 1Doctoral School of Health Sciences, University of Debrecen, 4032 Debrecen, Hungary.

Insights

This review of coronary heart disease (CHD) models found many studies but limited clinical evidence. More validation is needed for prognostic models predicting CHD risk using conventional and genetic factors.

Area of Science:

  • Cardiovascular Disease Epidemiology
  • Biostatistics and Health Informatics
  • Genomic Medicine

Background:

  • Multivariable prognostic models are crucial for predicting coronary heart disease (CHD) risk in the general population.
  • Existing models often use conventional risk factors, with emerging interest in incorporating genomic data.
  • A comprehensive overview and performance comparison of these models are lacking.

Purpose of the Study:

  • To systematically review and compare multivariable prognostic models for CHD in the general population.
  • To assess the performance of existing models based on discrimination, reclassification, and calibration.
  • To identify gaps and provide recommendations for future prognostic modeling research in CHD.

Main Methods:

  • Systematic literature review conducted across Embase, PubMed, Cochrane, Web of Science, and Scopus databases up to November 2019.
  • Inclusion criteria focused on prognostic studies of multivariable models for CHD using conventional and/or genomic risk factors.
  • Eligible studies (72 out of 4021 screened) were evaluated using CHARM and GRIPS statements for consistency and reliability.

Main Results:

  • Most identified models were developed in North America and targeted the general population.
  • Common predictors included age, sex, smoking, cholesterol, blood pressure, BMI, and diabetes.
  • Significant heterogeneity in CHD event definitions was noted, and the clinical utility of most models remains undemonstrated.

Conclusions:

  • While incorporating genetic risk scores shows potential for improved CHD incidence prediction, the generalizability of current models is uncertain.
  • There is a critical need for robust validation studies to enhance the quality, transparency, and clinical applicability of CHD prognostic models.
  • Further research should address heterogeneity in outcome definitions and rigorously validate models before widespread clinical adoption.

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