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Table 3 Relationships between CYP3A4 and CYP11A1 polymorphism and ischemic stroke risk

From: CYP3A4 and CYP11A1 variants are risk factors for ischemic stroke: a case control study

Gene SNP ID

Model

Genotype

Case

Control

Adjusted by age and gender

OR (95%CI)

p

CYP3A4

rs3735451

Allele

T

705

686

1.00

0.039

C

249

300

0.81 (0.66–0.98)

Genotype

TT

256

228

1.00

 

CT

193

230

0.74 (0.57–0.97)

0.029

CC

28

35

0.66 (0.38–1.14)

0.135

Dominant

TT

256

228

1.00

0.018

CT-CC

221

265

0.73 (0.56–0.95)

Recessive

TT-CT

449

458

1.00

0.308

CC

28

35

0.76 (0.45–1.29)

Log-additive

0.78 (0.63–0.96)

0.019

CYP3A4

rs4646440

Allele

G

768

754

1.00

0.046

A

186

228

0.80 (0.64–1.00)

Genotype

GG

307

282

1.00

 

GA

154

190

0.72 (0.55–0.95)

0.021

AA

16

19

0.72 (0.36–1.45)

0.362

Dominant

GG

307

282

1.00

0.017

GA-AA

170

209

0.72 (0.55–0.94)

Recessive

GG-GA

461

472

1.00

0.560

AA

16

19

0.81 (0.41–1.62)

Log-additive

0.77 (0.61–0.97)

0.024

  1. SNP single nucleotide polymorphism, OR odds ratio, 95% CI 95% confidence interval
  2. p values were calculated by logistic regression analysis with adjustments for age and gender
  3. p < 0.05 means the data is statistically significant
  4. Bold indicates that the values have statistical significance