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Table 7 Correlation between STAT4 gene polymorphism and the occurrence of diabetes complications

From: Association between STAT4 gene polymorphism and type 2 diabetes risk in Chinese Han population

SNP ID

Model

Genotype

T2D complicated with nephropathy

T2D complicated with CHD

DN

No DN

OR (95% CI)

p

Case

Control

OR (95% CI)

p

rs3821236

Allele

A

127

352

0.78(0.59–1.02)

0.073

127

352

1.14(0.86–1.52)

0.359

  

G

165

356

1.00

 

125

396

1.00

 
 

Genotype

AA

30

83

0.65(0.37–1.14)

0.131

30

83

1.41(0.77–2.60)

0.266

  

AG

67

186

0.62(0.40–0.99)

0.024*

67

186

1.35(0.81–2.25)

0.251

  

GG

49

85

1.00

 

29

105

1.00

 
 

Dominant

AA-AG

97

269

0.63(0.41–0.97)

0.037*

97

269

1.37(0.84–2.23)

0.207

  

GG

49

85

1.00

 

29

105

1.00

 
 

Recessive

AA

30

83

0.88(0.54–1.42)

0.589

30

83

1.16(0.70–1.91)

0.567

  

AG-GG

116

271

1.00

 

96

291

1.00

 
 

Log-additive

0.79(0.59–1.05)

0.099

1.19(0.88–1.61)

0.252

rs11893432

Allele

G

131

352

0.82(0.63–1.08)

0.163

126

357

1.10(0.82–1.46)

0.532

  

C

161

356

1.00

 

126

391

1.00

 
 

Genotype

GG

30

86

0.71(0.40–1.24)

0.227

30

86

1.29(0.70–2.35)

0.416

  

GC

71

180

0.78(0.49–1.23)

0.280

66

185

1.26(0.76–2.10)

0.371

  

CC

45

88

1.00

 

30

103

1.00

 
 

Dominant

GG-GC

101

266

0.75(0.49–1.17)

0.203

96

271

1.27(0.78–2.06)

0.334

  

CC

45

88

1.00

 

30

103

1.00

 
 

Recessive

GG

30

86

0.83(0.51–1.35)

0.455

30

86

1.10(0.67–1.81)

0.704

  

GC-CC

116

268

1.00

 

96

288

1.00

 
 

Log-additive

0.84(0.63–1.11)

0.212

1.14(0.84–1.53)

0.402

rs11889341

Allele

T

97

258

0.87(0.65–1.16)

0.333

81

274

0.82(0.61–1.11)

0.198

  

C

195

450

1.00

 

171

474

1.00

 
 

Genotype

TT

15

38

0.81(0.41–1.62)

0.558

10

43

0.56(0.25–1.25)

0.156

  

TC

67

182

0.79(0.52–1.21)

0.280

61

188

0.89(0.57–1.37)

0.589

  

CC

64

134

1.00

 

55

143

1.00

 
 

Dominant

TT-TC

82

220

0.80(0.54–1.19)

0.268

71

231

0.82(0.54–1.26)

0.370

  

CC

64

134

1.00

 

55

143

1.00

 
 

Recessive

TT

15

38

0.92(0.48–1.77)

0.807

10

43

0.60(0.28–1.28)

0.188

  

TC-CC

131

316

1.00

 

116

331

1.00

 
 

Log-additive

0.86(0.63–1.17)

0.339

0.80(0.58–1.12)

0.192

rs7574865

Allele

T

96

251

0.89(0.67–1.19)

0.437

82

265

0.88(0.65–1.19)

0.405

  

G

196

457

1.00

 

170

483

1.00

 
 

Genotype

TT

14

35

0.90(0.45–1.83)

0.775

9

40

0.65(0.29–1.47)

0.302

  

TG

68

181

0.84(0.55–1.27)

0.410

64

185

1.04(0.67–1.61)

0.869

  

GG

64

138

1.00

 

53

149

1.00

 
 

Dominant

TT-TG

82

216

0.85(0.57–1.27)

0.423

73

225

0.97(0.63–1.48)

0.882

  

GG

64

138

1.00

 

53

149

1.00

 
 

Recessive

TT

14

35

0.99(0.51–1.94)

0.980

9

40

0.64(0.29–1.39)

0.259

  

TG-GG

132

319

1.00

 

117

334

1.00

 
 

Log-additive

0.91(0.66–1.24)

0.530

0.90(0.65–1.25)

0.524

rs897200

Allele

C

147

342

1.09(0.83–1.43)

0.558

129

360

1.13(0.85–1.5)

0.400

  

T

145

366

1.00

 

123

388

1.00

 
 

Genotype

CC

35

90

1.10(0.63–1.93)

0.741

35

90

1.16(0.65–2.07)

0.605

  

CT

77

162

1.44(0.89–2.33)

0.139

59

180

1.05(0.63–1.75)

0.852

  

TT

34

102

1.00

 

32

104

1.00

 
 

Dominant

CC-CT

112

252

1.32(0.83–2.07)

0.239

94

270

1.09(0.68–1.75)

0.725

  

TT

34

102

1.00

 

32

104

1.00

 
 

Recessive

CC

35

90

0.87(0.55–1.38)

0.545

35

90

1.13(0.70–1.82)

0.617

  

CT-TT

111

264

1.00

 

91

284

1.00

 
 

Log-additive

1.05(0.80–1.38)

0.717

1.08(0.81–1.44)

0.606

  1. CHD coronary heart disease, CI confidence interval, OR odds ratio
  2. p values were calculated by unconditional logistic regression analysis with adjustment for age and gender; *p < 0.05 indicates statistical significance