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. Author manuscript; available in PMC: 2024 Mar 1.
Published in final edited form as: Clin Pharmacol Ther. 2022 Nov 19;113(3):615–623. doi: 10.1002/cpt.2776

Table 2.

CYP2C19 metabolizer phenotype and P2Y12 inhibitor at time of event or last follow-up by race and phenotype

Patient Group Total No. No. (%) IM/PMs No. (%) NM/RM/UMs IM/PM NM/RM/UM
Clopidogrel Alternative Therapy Clopidogrel Alternative Therapy
All Patients 3342 1032 (30.9) 2310 (69.1) 461 (44.7) 571 (55.3) 1932 (83.6) 378 (16.4)
White 2448 728 (29.7) 1720 (70.3) 315 (43.3) 413 (56.7) 1433 (83.3) 287 (16.7)
Black 659 226 (34.3) 433 (65.7) 109 (48.2) 117 (51.8) 371 (85.7) 62 (14.3)
Asian, Native Hawaiian or Pacific Islander* 43 20 (46.5) 23 (53.5) 10 (50) 10 (50) 19 (82.6) 4 (17.4)
American Indian or Alaska Native 36 17 (47.2) 19 (52.8) 11 (64.7) 6 (35.3) 13 (68.4) 6 (31.6)
Multiracial 32 9 (28.1) 23 (71.9) 5 (55.6) 4 (44.4) 20 (87.0) 3 (13.0)
Unknown race 124 32 (25.8) 92 (74.2) 11 (34.4) 21 (65.6) 76 (82.6) 16 (17.4)

Data are presented as number (%)

*

Combined because of the small number of Native Hawaiian or Pacific Islander patients (n=5)

p,0.001 for comparison of alternative therapy in IM/PMs versus NM/RM/UMs.

IM, intermediate metabolizer; NM, normal metabolizer; PM, poor metabolizer; RM, rapid metabolizer; UM, ultra-rapid metabolizer