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Table 3 Allele and genotype distribution of HPA polymorphisms in CAD patients and healthy controls

From: Association of human platelet alloantigens encoding gene polymorphisms with the risk of Coronary artery disease in Iranian patients

dbSNP

Alleles/genotypes

CAD (n = 200)

N (%)

Control (n = 100)

N (%)

χ2

P value

OR (95% CI)

HPA1

T (a)

363 (90.7)

178 (89)

0.460

0.497

1.212 (0.69–2.11)

C (b)

37 (9.3)

22 (11)

–

–

0.824 (0.47–1.43)

TT (aa)

163 (81.5)

79 (78)

0.516

0.472

1.242 (0.68–2.24)

CT (ab)

37 (18.5)

22 (22)

–

–

0.804 (0.44–1.45)

CC (bb)

0 (0)

0 (0)

–

–

–

HWE

  

P = 0.216

   

HPA2

C (a)

350 (87.5)

178 (89)

0.284

0.594

0.865 (0.50–1.47)

T (b)

50 (12.5)

22 (11)

–

–

1.155 (0.67–1.96)

CC (aa)

153(76.5)

79 (79)

0.303

0.859

0.865 (0.48–1.54)

CT (ab)

44 (22)

20 (20)

–

–

1.128 (0.62–2.04)

TT (bb)

3 (1.5)

1 (1)

–

–

1.507 (0.15–14.68)

HWE

  

P = 0.830

   

HPA3

T (a)

235 (58.8)

118 (59)

0.003

0.953

0.989 (0.70–1.39)

G (b)

165 (41.2)

82 (41)

–

–

1.010 (0.71–1.42)

TT (aa)

74 (37)

38 (38)

0.061

0.969

0.958 (0.58–1.57)

GT (ab)

87 (43.5)

42 (42)

–

–

1.063 (0.65–1.72)

GG (bb)

39 (19.5)

20 (20)

–

–

0.968 (0.53–1.76)

HWE

  

P = 0.187

   

HPA4

G (a)

400 (100)

200 (100)

–

–

–

A (b)

0 (0)

0 (0)

–

–

–

GG (aa)

200 (100)

100

–

–

–

GA (ab)

0 (0)

0

–

–

–

AA (bb)

0 (0)

0

–

–

–

HWE

  

P = 0

   

HPA5

G (a)

363 (90.7)

183 (91.5)

0.091

0.762

0.911 (0.49–1.66)

A (b)

37 (9.2)

17 (8.5)

–

–

1.097 (0.60–2.00)

GG (aa)

167 (83.5)

85 (85)

0.125

0.939

0.893 (0.45–1.73)

AG (ab)

29 (14.5)

13 (13)

–

–

1.135 (0.56–2.29)

AA (bb)

4 (2)

2 (2)

–

–

0.951 (0.17–5.28)

HWE

  

P = 0.1

   

HPA6

G (a)

400 (100)

200 (100)

–

–

–

A (b)

0 (0)

0 (0)

–

–

–

GG (aa)

200 (100)

100

–

–

–

GA (ab)

0 (0)

0

–

–

–

AA (bb)

0 (0)

0

–

–

–

HWE

  

P = 0

   

HPA9

G (a)

400 (100)

200 (100)

–

–

–

A (b)

0 (0)

0 (0)

–

–

–

GG (aa)

200 (100)

100

–

–

–

GA (ab)

0 (0)

0

–

–

–

AA (bb)

0 (0)

0

–

–

–

HWE

  

P = 0

   

HPA15

C (a)

188 (47)

88 (44)

0.483

0.487

1.128 (0.80–1.58)

A (b)

212 (53)

112 (56)

–

–

0.886 (0.62–1.24)

CC (aa)

43 (21.5)

21 (21)

1.033

0.596

1.030 (0.57–1.85)

AC (ab)

102 (51)

46 (46)

–

–

1.221 (0.75–1.97)

AA (bb)

55 (27.5)

33 (33)

–

–

0.770 (0.45–1.29)

HWE

  

P = 0.505

   
  1. SNP single nucleotide polymorphism, CAD coronary arthery disease, HWE Hardy–Weinberg equilibrium