The figure shows reclassification results when protein risk score and polygenic risk scores are added on top of clinical risk factors (age, sex, statin use, hypertension treatment, type 2 diabetes, body mass index [calculated as weight in kilograms divided by height in meters squared], and smoking status at the time of plasma collection) in the primary event population test set (4018 participants; 465 events; 284 events within 10 years). The results are shown for predicted 10-year risk using a 7.5% risk threshold to separate between low and intermediate risk. Three groups are considered: (i) those with an atherosclerotic cardiovascular disease (ASCVD) event within 10 years; (ii) those who die of causes other than ASCVD within 10 years; and (iii) those who survive 10 years without an ASCVD event.
Panel A shows a reclassification table for the addition of protein risk score on top of the clinical risk factors. The total categorical net reclassification improvement is 0.040 (95% CI, −0.009 to 0.094) and 0.044 (95% CI, −0.013 to 0.096) when excluding those who die from non-ASCVD causes. Net reclassification improvement for ASCVD events is −0.007 (95% CI, −0.056 to 0.046), 0.047 (95% CI, 0.035 to 0.059) for ASCVD nonevents (groups [ii] and [iii]), and 0.052 (95% CI, 0.039 to 0.064) for those who survive 10 years without ASCVD event (group [iii]).
Panel B shows a reclassification table when both protein risk score and polygenic risk scores are added on top of the clinical risk factors. The total net reclassification improvement is 0.053 (95% CI, −0.006 to 0.110) and 0.056 (95% CI, −0.001 to 0.114) when excluding those who die from non-ASCVD causes. Net reclassification improvement for ASCVD events is 0.004 (95% CI, −0.054 to 0.058), 0.049 (95% CI, 0.037 to 0.061) for ASCVD nonevents (groups [ii] and [iii]), and 0.053 (95% CI, 0.039 to 0.066) for those who survive 10 years without ASCVD event (group [iii]).