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Table 4 The relationship of FGFR2 and MGAT5 SNPs with COPD risk stratified by smoking

From: The polymorphisms of FGFR2 and MGAT5 affect the susceptibility to COPD in the Chinese people

Gene SNP

Model

Genotype

Smoking

No smoking

Frequency in case

Frequency in control

OR (95% CI)

p

Frequency in case

Frequency in control

OR(95% CI)

p

FGFR2

rs2420915

Allele

G

0.613

0.615

1.00

 

0.567

0.674

1.00

 

A

0.387

0.385

1.01 (0.64–1.60)

0.966

0.433

0.326

1.58 (1.11–2.24)

0.010

Codominant

GG

0.370

0.385

1.00

 

0.291

0.458

1.00

 

AA

0.144

0.154

1.07 (0.40–2.87)

0.894

0.158

0.110

2.16 (0.99–4.68)

0.052

AG

0.486

0.461

1.11 (0.55–2.23)

0.781

0.551

0.432

1.96 (1.16–3.29)

0.012

Dominant

GG

0.370

0.385

1.00

 

0.291

0.458

1.00

 

AA + AG

0.630

0.615

1.10 (0.57–2.12)

0.785

0.709

0.542

2.00 (1.21–3.28)

0.006

Recessive

AG + GG

0.856

0.846

1.00

 

0.842

0.890

1.00

 

AA

0.144

0.154

1.01 (0.41–2.53)

0.977

0.158

0.110

1.46 (0.72–3.00)

0.297

Additive

1.05 (0.66–1.68)

0.836

1.60 (1.10–2.31)

0.013

FGFR2

rs1907240

Allele

A

0.617

0.577

1.00

 

0.542

0.640

1.00

 

G

0.383

0.423

0.85 (0.54–1.33)

0.470

0.458

0.360

1.50 (1.07–2.11)

0.020

Codominant

AA

0.407

0.327

1.00

 

0.301

0.381

1.00

 

GG

0.172

0.173

0.92 (0.35–2.40)

0.859

0.217

0.102

2.63 (1.22–5.68)

0.014

GA

0.421

0.500

0.68 (0.33–1.38)

0.282

0.482

0.517

1.19 (0.70–2.01)

0.525

Dominant

AA

0.407

0.327

1.00

 

0.301

0.381

1.00

 

GG + GA

0.593

0.673

0.73 (0.37–1.44)

0.366

0.699

0.619

1.43 (0.86–2.35)

0.165

Recessive

GA + AA

0.828

0.827

1.00

 

0.783

0.898

1.00

 

GG

0.172

0.173

1.14 (0.48–2.72)

0.769

0.217

0.102

2.38 (1.17–4.81)

0.016

Additive

0.90 (0.58–1.41)

0.645

1.51 (1.06–2.14)

0.023

FGFR2

rs2257129

Allele

C

0.627

0.577

1.00

 

0.552

0.640

1.00

 
 

T

0.373

0.423

0.81 (0.52–1.28)

0.371

0.448

0.360

1.45 (1.03–2.04)

0.035

Codominant

CC

0.390

0.327

1.00

 

0.303

0.381

1.00

 

TT

0.137

0.173

0.75 (0.28–2.02)

0.572

0.200

0.102

2.40 (1.11–5.23)

0.027

TC

0.473

0.500

0.79 (0.39–1.61)

0.517

0.497

0.517

1.21 (0.72–2.05)

0.468

Dominant

CC

0.390

0.327

1.00

 

0.303

0.381

1.00

 

TT + TC

0.610

0.673

0.78 (0.40–1.54)

0.474

0.697

0.619

1.41 (0.86–2.33)

0.177

Recessive

TC + CC

0.863

0.827

1.00

 

0.800

0.898

1.00

 

TT

0.137

0.173

0.86 (0.35–2.11)

0.742

0.200

0.102

2.14 (1.05–4.36)

0.036

Additive

0.85 (0.53–1.36)

0.499

1.46 (1.02–2.09)

0.039

MGAT5

rs6430491

Allele

G

0.588

0.606

1.00

 

0.699

0.576

1.00

 

A

0.412

0.394

1.08 (0.68–1.70)

0.757

0.301

0.424

0.59 (0.41–0.83)

0.003

Codominant

GG

0.333

0.365

1.00

 

0.452

0.364

1.00

 

AA

0.156

0.154

1.11 (0.42–2.91)

0.839

0.054

0.212

0.21 (0.09–0.49)

0.0003

AG

0.511

0.481

1.28 (0.63–2.62)

0.495

0.494

0.424

0.92 (0.55–1.55)

0.758

Dominant

GG

0.333

0.365

1.00

 

0.452

0.364

1.00

 

AA + AG

0.667

0.635

1.24 (0.63–2.42)

0.537

0.548

0.636

0.69 (0.42–1.12)

0.136

Recessive

AG + GG

0.844

0.846

1.00

 

0.946

0.788

1.00

 

AA

0.156

0.154

0.96 (0.40–2.32)

0.927

0.054

0.212

0.22 (0.10–0.49)

0.0002

Additive

1.10 (0.68–1.76)

0.704

0.58 (0.40–0.83)

0.003

MGAT5

rs2593704

Allele

C

0.789

0.635

1.00

 

0.777

0.770

1.00

 

G

0.211

0.365

0.46 (0.29–0.76)

0.002

0.223

0.230

0.96 (0.64–1.43)

0.834

Codominant

CC

0.639

0.404

1.00

 

0.602

0.609

1.00

 

GG

0.061

0.135

0.37 (0.12–1.16)

0.088

0.048

0.070

0.73 (0.26–2.04)

0.544

GC

0.300

0.461

0.42 (0.21–0.84)

0.014

0.350

0.321

1.09 (0.65–1.82)

0.756

Dominant

CC

0.639

0.404

1.00

 

0.602

0.609

1.00

 

GG + GC

0.361

0.596

0.41 (0.21–0.79)

0.008

0.398

0.391

1.02 (0.63–1.67)

0.930

Recessive

GC + CC

0.939

0.865

1.00

 

0.952

0.930

1.00

 

GG

0.061

0.135

0.54 (0.18–1.62)

0.268

0.048

0.070

0.71 (0.26–1.95)

0.501

Additive

0.53 (0.32–0.87)

0.012

0.96 (0.65–1.43)

0.850

  1. SNP single nucleotide polymorphism, OR odds ratio, 95% CI 95% confidence interval
  2. p values were calculated by logistic regression analysis with adjustment for age and gender
  3. Bold values indicate statistical significance (p < 0.05)