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Table 3 Associations between IL-6 polymorphisms and ONFH susceptibility

From: An intron SNP rs2069837 in IL-6 is associated with osteonecrosis of the femoral head development

SNP

Model

Genotype

Control

Case

OR (95% CI)

p

rs2069837

Allele

A

873 (77.3%)

925 (81.7%)

1.00

 
 

G

257 (22.7%)

207 (18.3%)

0.76 (0.62–0.93)

0.009

Codominant

AA

336 (59.5%)

378 (66.8%)

1.00

 
 

GG

28 (5%)

19 (3.4%)

0.61 (0.33–1.11)

0.103

 

AG

201 (35.6%)

169 (29.9%)

0.75 (0.58–0.96)

0.023

Dominant

AA

336 (59.5%)

378 (66.8%)

1.00

 
 

GG + AG

229 (40.5%)

188 (33.2%)

0.73 (0.57–0.93)

0.011

Recessive

AA + AG

537 (95%)

547 (96.6%)

1.00

 
 

GG

28 (5%)

19 (3.4%)

0.67 (0.37–1.21)

0.186

Additive

/

  

0.76 (0.62–0.93)

0.009

rs13306435

Allele

T

1089 (96.2%)

1094 (96.6%)

1.00

 
 

A

43 (3.8%)

38 (3.4%)

0.88 (0.56–1.37)

0.572

Codominant

TT

524 (92.6%)

528 (93.3%)

1.00

 
 

AA

1 (0.2%)

0 (0%)

/

/

 

AT

41 (7.2%)

38 (6.7%)

0.92 (0.58–1.45)

0.712

Dominant

TT

524 (92.6%)

528 (93.3%)

1.00

 
 

AA + AT

42 (7.4%)

38 (6.7%)

0.90 (0.57–1.41)

0.634

Recessive

TT + AT

565 (99.8%)

566 (100%)

1.00

 
 

AA

1 (0.2%)

0 (0%)

/

/

Additive

/

  

0.88 (0.56–1.37)

0.560

  1. Bold indicates statistical signifcance (p < 0.05)
  2. SNP single nucleotide polymorphism, OR odds ratio, CI confidence interval
  3. p values were calculated by logistic regression analysis adjusted age and sex