Aims The European Systematic Coronary Risk Evaluation 2 (SCORE2) and SCORE2-Older Persons (OP) models are recommended to identify individuals at high 10-year risk for cardiovascular disease (CVD). Independent validation and assessment of clinical utility is needed. This study aims to assess discrimination, calibration, and clinical utility of low-risk SCORE2 and SCORE2-OP.Methods and results Validation in individuals aged 40-69 years (SCORE2) and 70-79 years (SCORE2-OP) without baseline CVD or diabetes from the European Prospective Investigation of Cancer (EPIC) Norfolk prospective population study. We compared 10-year CVD risk estimates with observed outcomes (cardiovascular mortality, non-fatal myocardial infarction, and stroke). For SCORE2, 19 560 individuals (57% women) had 10-year CVD risk estimates of 3.7% [95% confidence interval (CI) 3.6-3.7] vs. observed 3.8% (95% CI 3.6-4.1) [observed (O)/expected (E) ratio 1.0 (95% CI 1.0-1.1)]. The area under the curve (AUC) was 0.75 (95% CI 0.74-0.77), with underestimation of risk in men [O/E 1.4 (95% CI 1.3-1.6)] and overestimation in women [O/E 0.7 (95% CI 0.6-0.8)]. Decision curve analysis (DCA) showed clinical benefit. Systematic Coronary Risk Evaluation 2-Older Persons in 3113 individuals (58% women) predicted 10-year CVD events in 10.2% (95% CI 10.1-10.3) vs. observed 15.3% (95% CI 14.0-16.5) [O/E ratio 1.6 (95% CI 1.5-1.7)]. The AUC was 0.63 (95% CI 0.60-0.65) with underestimation of risk across sex and risk ranges. Decision curve analysis showed limited clinical benefit.Conclusion In a UK population cohort, the SCORE2 low-risk model showed fair discrimination and calibration, with clinical benefit for preventive treatment initiation decisions. In contrast, in individuals aged 70-79 years, SCORE2-OP demonstrated poor discrimination, underestimated risk in both sexes, and limited clinical utility.
机构:
Univ Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Natl Univ Hlth Syst, Dept Med, Singapore, SingaporeUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Lahiri, M.
Morgan, C.
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Univ Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, EnglandUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Morgan, C.
Luben, R. N.
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Univ Cambridge, Sch Clin Med, Dept Publ Hlth & Primary Care, Cambridge, EnglandUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Luben, R. N.
Bunn, D. K.
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Univ Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Univ E Anglia, Norfolk Arthrit Register, Norwich NR4 7TJ, Norfolk, EnglandUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Bunn, D. K.
Lunt, M.
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Univ Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, EnglandUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Lunt, M.
Verstappen, S. M.
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Univ Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, EnglandUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Verstappen, S. M.
Symmons, D. P.
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Univ Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, EnglandUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Symmons, D. P.
Khaw, K. -T.
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Univ Cambridge, Sch Clin Med, Dept Publ Hlth & Primary Care, Cambridge, EnglandUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Khaw, K. -T.
Wareham, N. J.
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Univ Cambridge, Sch Clin Med, Dept Publ Hlth & Primary Care, Cambridge, EnglandUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England
Wareham, N. J.
Bruce, I. N.
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Univ Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, EnglandUniv Manchester, Arthrit Res UK Epidemiol Unit, Manchester, Lancs, England