Skip to main content

Table 3 Distribution of CYP2C19 polymorphisms in MACE, no-MACE, bleeding, and no-bleeding patients

From: Association between cytochrome P450 2C19 polymorphism and clinical outcomes in clopidogrel-treated Uygur population with acute coronary syndrome: a retrospective study

Variables

Overall (n = 351)

MACE

(n = 101)

No-MACE (n = 250)

P value

Bleeding

(n = 18)

No-bleeding

(n = 333)

P value

Polymorphisms, n (%)

CYP2C19*2

       

 GG

251 (71.5)

58 (57.4)

193 (77.2)

0.001*

16 (88.9)

235 (70.6)

0.273

 GA

90 (25.6)

38 (37.6)

52 (20.8)

2 (11.1)

88 (26.4)

 AA

10 (2.9)

5 (5.0)

5 (2.0)

/

10 (3.0)

 A allele

110 (15.7)

48 (23.8)

62 (12.4)

 < 0.001*

2 (5.6)

108 (16.2)

0.139

 G allele

692 (84.3)

154 (76.2)

438 (87.6)

34 (94.4)

558 (83.8)

CYP2C19*3

       

 GG

328 (93.4)

91 (90.1)

237 (94.8)

0.107

16 (88.9)

312 (93.7)

0.333

 GA

23 (6.6)

10 (9.9)

13 (5.2)

2 (11.1)

21 (6.3)

 AA

/

/

/

/

/

 

 A allele

23 (3.3)

10 (5.0)

13 (2.6)

0.113

2 (5.6)

21 (3.2)

0.332

 G allele

679 (96.7)

192 (95.0)

487 (97.4)

34 (94.4)

645 (96.8)

CYP2C19*17

       

 CC

252 (71.8)

81 (80.2)

171 (68.4)

0.08

10 (55.6)

242 (72.7)

0.139

 CT

91 (25.9)

18 (17.8)

73 (29.2)

7 (38.9)

84 (25.2)

 TT

8 (2.3)

2 (2.0)

6 (2.4)

1 (5.6)

7 (2.1)

 T allele

107 (15.2)

22 (10.9)

85 (17.0)

0.041*

9 (25.0)

98 (14.7)

0.094

 C allele

595 (84.8)

180 (89.1)

415 (83.0)

27 (75.0)

568 (85.3)

Metabolizer Phenotype, n (%)

 EMs

147 (41.9)

37 (36.6)

110 (41.6)

0.205

7 (38.9)

140 (42.0)

0.792

 IMs

107 (30.5)

43 (42.6)

64 (25.6)

0.002*

4 (22.2)

103 (30.9)

0.601

 PMs

12 (3.4)

7 (6.9)

5 (2.0)

0.021*

/

12 (3.6)

1.0

 UMs

85 (24.2)

14 (13.9)

71 (28.4)

0.004*

7 (38.9)

78 (23.4)

0.158

  1. MACE major adverse cardiac events, EMs extensive metabolizers, IMs intermediate metabolizers, PMs poor metabolizers, UMs ultra-metabolizers; *P < 0.05,* the difference of MACE vs. no-MACE by χ2 test at 0.05