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. 2018 Jan 19;8:1229. doi: 10.1038/s41598-017-18134-y

Table 1.

Prevalence of genetic variants and their risk analysis for high OPR.

N (%) Adjusted OR (95% CI)* p-value
CYP2C19 *1/*1 1682 (36.7) Reference
*1/*17 56 (1.2) 1.71 (0.906–3.245) 0.10
*1/*2 1610 (35.1) 2.01 (1.675–2.418) <0.01
*1/*3 561 (12.2) 2.31 (1.818–2.933) <0.01
*1/*R 2227 (48.6) 2.08 (1.749–2.466) <0.01
*2/*17 33 (0.7) 2.43 (1.094–5.396) 0.03
*2/*2 342 (7.5) 3.86 (2.943–5.062) <0.01
*2/*3 245 (5.3) 4.43 (3.265–6.022) <0.01
*3/*17 9 (0.2) 1.90 (0.375–9.646) 0.44
*3/*3 49 (1.1) 7.59 (4.135–13.935) <0.01
*R/*R 678 (14.8) 4.14 (3.339–5.141) <0.01
CYP2C9 *1/*1 4226 (92.1) Reference
*1/*3 356 (7.8) 0.76 (0.574–1.005) 0.80
*3/*3 5 (0.1) 0.78 (0.083–7.217) 0.90
PON1 RR 552 (12.0) Reference
QR 2172 (47.4) 0.83 (0.659–1.035) 0.08
QQ 1863 (40.6) 0.90 (0.719–1.136) 0.95
ABCB1 CC 1865 (40.7) Reference
CT 2101 (45.8) 1.05 (0.898–1.220) 0.36
TT 621 (13.5) 0.95 (0.758–1.189) 0.49
P2Y12 GG 3483 (75.9) Reference
GT 1007 (22.0) 1.00 (0.837–1.183) 0.52
TT 97 (2.1) 1.19 (0.746–1.900) 0.46

*Odd ratio (OR) with 95% confidence interval (CI) was adjusted for age, sex, body mass index, current smoker, diabetes mellitus, prior coronary artery bypass graft, acute coronary syndrome, multivessel involvement, haemoglobin level, and creatinine level.