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. 2021 Oct 4;2(12):100364. doi: 10.1016/j.patter.2021.100364

Table 1.

Baseline characteristics and predicted 10-year risk of cardiovascular events in UK Biobank

Development (N = 138,619) Holdout (N = 34,655)
Age (years) 56.2 (8.1) 56.1 (8.1)
Males 70,896 (51.1%) 17,606 (50.9%)

Ethnicity

White 132,610 (95.7%) 33,092 (95.5%)
Black 1,945 (1.4%) 499 (1.4%)
East Asian 1,095 (0.8%) 290 (0.8%)
South Asian 1,614 (1.2%) 402 (1.2%)
Other 1,355 (1.0%) 372 (1.1%)
Current smoker 14,501 (10.5%) 3,604 (10.4%)
Diabetes 6,568 (4.7%) 1,635 (4.7%)
Cholesterol (mg/dL) 217.5 (37.8) 217.4 (37.6)
HDL-C (mg/dL) 55.4 (13.9) 55.3 (13.9)
LDL-C (mg/dL) 136.3 (29.2) 136.2 (29.0)
SBP (mm Hg) 137.5 (18.4) 137.3 (18.3)
Antihypertensive 26,100 (18.8%) 6,501 (18.8%)
Genome-wide polygenic score for CAD(GPSCAD) −0.03 (0.99) −0.03 (0.99)
Incident CAD events over median 11-year follow-up 4,103 (3.0%) 1,037 (3.0%)

Predicted 10-year risk (%)

FRS 6.9 (6.4) 6.9 (6.4)
PCE 8.3 (7.7) 8.2 (7.7)
QRISK3-2017 (QRISK3) 10.0 (8.4) 9.9 (8.4)

The development cohort was used for a 5-fold cross-validation procedure to build ML4HEN-COX, while the holdout cohort was used to test performance in unseen data (Figure 1). GPSCAD was adjusted for the first four PCs of genetic ancestry and scaled to mean 0 and standard deviation 1. None of the above variables were significantly different between groups at the p < 0.05 level. HDL-C, high-density lipoprotein cholesterol; LDL-C, low-density lipoprotein cholesterol; SBP, systolic blood pressure.