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An Office-Based Cardiovascular Prediction Model Developed and Validated in Cohort Studies of a Middle-Income Country Publisher Pubmed



Fahimfar N1, 2 ; Malekzadeh R3 ; Fotouhi A1 ; Mansournia MA1 ; Sarrafzadegan N4, 5 ; Azizi F6 ; Sepanlou SG3 ; Mansourian M4 ; Hadaegh F7 ; Emamian MH8 ; Poustchi H3 ; Talaei M4, 9 ; Pourshams A3 ; Roohafza H10 Show All Authors
Authors
  1. Fahimfar N1, 2
  2. Malekzadeh R3
  3. Fotouhi A1
  4. Mansournia MA1
  5. Sarrafzadegan N4, 5
  6. Azizi F6
  7. Sepanlou SG3
  8. Mansourian M4
  9. Hadaegh F7
  10. Emamian MH8
  11. Poustchi H3
  12. Talaei M4, 9
  13. Pourshams A3
  14. Roohafza H10
  15. Sharafkhah M3
  16. Samavat T11
  17. Lotfaliany M12
  18. Steyerberg EW13, 14
  19. Khalili D7, 15
Show Affiliations
Authors Affiliations
  1. 1. Department of Epidemiology and Biostatistics, School of Public Health, Tehran University of Medical Sciences, Tehran, Iran
  2. 2. Osteoporosis Research Center, Endocrinology and Metabolism Clinical Sciences Institute, Tehran University of Medical Sciences, Tehran, Iran
  3. 3. Digestive Diseases Research Center, Digestive Diseases Research Institute, Tehran University of Medical Sciences, Tehran, Iran
  4. 4. Isfahan Cardiovascular Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
  5. 5. School of Population and Public Health, Faculty of Medicine, University of British Columbia, Vancouver, BC, Canada
  6. 6. Endocrine Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  7. 7. Prevention of Metabolic Disorders Research Center, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran
  8. 8. Ophthalmic Epidemiology Research Center, Shahroud University of Medical Sciences, Shahroud, Iran
  9. 9. Institute of Population Health Sciences, Barts and The London School of Medicine and Dentistry, Queen Mary University of London, UK, London, United Kingdom
  10. 10. Cardiac Rehabilitation Research Center, Cardiovascular Research Institute, Isfahan University of Medical Sciences, Isfahan, Iran
  11. 11. Office for Prevention & Control of Heart Diseases, Center for Non-communicable Diseases Control, Ministry of Health, Iran
  12. 12. Biostatistics Unit, Deakin University, Geelong, VIC, Australia
  13. 13. Department of Biomedical Data Sciences, sections Medical Statistics and Medical Decision Making, Leiden University Medical Centre, Leiden, Netherlands
  14. 14. Department of Public Health, Erasmus University Medical Center, Rotterdam, Netherlands
  15. 15. Department of Biostatistics and Epidemiology, Research Institute for Endocrine Sciences, Shahid Beheshti University of Medical Sciences, Tehran, Iran

Source: Journal of Clinical Epidemiology Published:2022


Abstract

Objective: Prediction models for cardiovascular disease (CVD) mortality come from high-income countries, comprising laboratory measurements, not suitable for resource-limited countries. This study aims to develop and validate a non-laboratory model to predict CVD mortality in a middle-income setting. Study design and setting: We used data of population aged 40-80 years from three cohort studies: Tehran Lipid and Glucose Study (n = 5160), Isfahan Cohort Study (n = 4350), and Golestan Cohort Study (n = 45,500). Using Cox proportional hazard models, we developed prediction models for men and women, separately. Cross-validation and bootstrapping procedures were applied. The models’ discrimination and calibration were assessed by concordance statistic (C-index) and calibration plot, respectively. We calculated the models' sensitivity, specificity and net benefit fraction in a threshold probability of 5%. Results: The 10-year CVD mortality risks were 5.1% (95%CI: 4.8-5.5) in men and 3.1% (95%CI: 2.9%-3.3%) in women. The optimism-corrected performance of the model was c = 0.774 in men and c = 0.798 in women. The models showed good calibration in both sexes, with a predicted-to-observed ratio of 1.07 in men and 1.09 in women. The sensitivity was 0.76 in men and 0.66 in women. The net benefit fraction was higher in men compared to women (0.46 vs. 0.35). Conclusion: A low-cost model can discriminate well between low- and high-risk individuals, and can be used for screening in low-middle income countries. © 2021 Elsevier Inc.
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