Skip to main content

Table 2 Analysis of association between ischemic stroke risk and ten APOD and SIGMAR1 SNPs

From: Variations in apolipoprotein D and sigma non-opioid intracellular receptor 1 genes with relation to risk, severity and outcome of ischemic stroke

SNP*

Allele pair

Control subj. number of genotypes

IS patients number of genotypes

Crude OR (95% CI)

Multiple LR** OR (95% CI)

SIGMAR1:

     

rs11559048

CC

1530

2695

0.51 (0.21-1.26)

0.58 (0.91-1.20)

 

CT

8

9

P = 0.145

P = 0.491

 

TT

1

-

  

rs1800866

TT

1128

2141

1.03 (0.92-1.16)

1.02 (0.90-1.16)

 

TG

401

795

P = 0.615

P = 0.768

 

GG

46

88

  

rs12001648

CC

1393

2420

0.95 (0.79-1.15)

0.85 (0.70-1.04)

 

CT

165

286

P = 0.595

P = 0.120

 

TT

9

8

  

rs7036351

GG

1130

1944

1.03 (0.91-1.16)

1.02 (0.89-1.16)

 

GA

399

693

P = 0.675

P = 0.789

 

AA

40

77

  

rs3808873

GG

833

1475

1.00 (0.89-1.11)

0.98 (0.88-1.10)

 

GA

491

887

P = 0.950

P = 0.779

 

AA

91

153

  

APOD :***

     

rs76929107

CC

1540

2943

1.06 (0.74-1.51)

1.10 (0.75-1.59)

 

CT

44

91

P = 0.761

P = 0.634

 

TT

1

1

  

rs5952

TT

1548

2710

1.90 (0.52-6.92)

2.23 (0.57-8.75)

 

TC

3

10

P = 0.329

P = 0.251

 

CC

-

-

  

rs34697430

GG

435

769

1.00 (0.92-1.09)

1.01 (0.92-1.11)

 

GA

784

1317

P = 0.966

P = 0.895

 

AA

349

623

  

rs7659

AA

803

1306

1.11 (1.01-1.22)

1.12 (1.01-1.25)

 

AG

617

1177

P = 0.038

P = 0.029

 

GG

130

240

  

rs823510

TT

880

1576

0.99 (0.89-1.09)

0.99 (0.89-1.11)

 

TG

590

981

P = 0.805

P = 0.884

 

GG

82

164

  
  1. *)All genotypes were conforming to the Hardy-Weinberg equilibrium criterion (with P = 0.093 or more when using a chi-square test on the control subjects), except for rs11559048 that showed a significant Hardy-Weinberg disequilibrium (P < 0.001).
  2. **)ORs obtained by multiple logistic regression analysis controlling for covariates age, gender, diabetes mellitus, hypertension and current smoking.
  3. ***)Two additional APOD encoding SNPs, rs5954 and rs5955, were genotyped but not included in this study due to monomorphic traits.