TABLE 3.
Biomarker combination |
N | Predicted events | C (old) | C (new) | P | NRI | P | IDI | P | |||
Ischemia-associated |
Bleeding-associated |
|||||||||||
biomarker |
biomarker |
|||||||||||
Name | Value | Name | Value | |||||||||
AST | 1 (> ULN) 0 (≤ ULN and ≥ LLN) -1 (< LLN) |
RDW-CV | 1 (> ULN) 0 (≤ ULN and ≥ LLN) -1 (< LLN) | 3,558 | Ischemia | 0.590 (0.560–0.610) | 0.600 (0.580–0.620) | 0.040 | 0.118 (0.028–0.175) | 0.016 | 0.005 (0–0.011) | 0.048 |
Bleeding | 0.560 (0.530–0.590) | 0.580 (0.550–0.610) | 0.030 | 0.090 (0.004–0.150) | 0.032 | 0.004 (0.001–0.009) | <0.001 |
Reported P-values were corrected using Benjamini-Hochberg method to account for multiple hypothesis testing. N, sample size; C (old), C statistic of DAPT score; C (new), C statistic of DAPT score plus incorporated biomarker combination. NRI, net reclassification improvement; IDI, integrated discrimination improvement; ULN, upper limit of reference range; LLN, lower limit of reference range; AST, aspartate aminotransferase; RDW-CV, red cell distribution width coefficient of variation.