An office-based cardiovascular prediction model developed and validated in cohort studies of a middle-income country

Noushin Fahimfar1, Reza Malekzadeh2, Akbar Fotouhi3

  • 1Department of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran; Osteoporosis Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran.

Insights

A new, low-cost cardiovascular disease (CVD) mortality prediction model was developed for middle-income countries. This non-laboratory model effectively identifies high-risk individuals for targeted screening and intervention.

Area of Science:

  • Cardiovascular epidemiology
  • Public health
  • Health economics

Background:

  • Existing cardiovascular disease (CVD) mortality prediction models often rely on laboratory measurements, limiting their applicability in resource-limited settings.
  • There is a critical need for accessible and cost-effective tools to predict CVD mortality in low- and middle-income countries (LMICs).

Purpose of the Study:

  • To develop and validate a non-laboratory-based model for predicting cardiovascular disease mortality.
  • To assess the model's performance in a middle-income population, ensuring its suitability for resource-constrained environments.

Main Methods:

  • Utilized data from three large cohort studies in Iran (Tehran Lipid and Glucose Study, Isfahan Cohort Study, Golestan Cohort Study) involving 40-80 year olds.
  • Developed separate Cox proportional hazard models for men and women, employing cross-validation and bootstrapping for robust validation.
  • Assessed model discrimination using the concordance statistic (C-index) and calibration via calibration plots, sensitivity, specificity, and net benefit fraction.

Main Results:

  • The 10-year CVD mortality risk was estimated at 5.1% for men and 3.1% for women.
  • The developed models demonstrated good discrimination, with optimism-corrected C-indices of 0.774 for men and 0.798 for women.
  • Models showed favorable calibration (predicted-to-observed ratios of 1.07 for men, 1.09 for women) and acceptable sensitivity (0.76 men, 0.66 women).

Conclusions:

  • A low-cost, non-laboratory prediction model effectively discriminates between individuals at low and high risk of CVD mortality.
  • This model is suitable for implementation in screening programs within low- and middle-income countries, addressing a significant public health need.
Abstract

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