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Table 5 Associations between AdipoQ gene polymorphisms and CHD risk

From: Single nucleotide polymorphism rs3774261 in the AdipoQ gene is associated with the risk of coronary heart disease (CHD) in Northeast Han Chinese population: a case-control study

SNPs

Models

OR

95%CI

P

AIC

rs3774261

Codominant

1.68

1.32–2.13

<0.0001

2058.1

  

1.90

1.41–2.54

<0.0001

 
 

Dominant

1.74

1.39–2.18

<0.0001

2056.9

 

Recessive

1.37

1.07–1.77

0.014

2074.6

 

Overdominant

1.29

1.06–1.59

0.013

2074.5

 

Log-additive

1.40

1.21–1.62

<0.0001

2059.7

rs1063537

Codominant

0.84

0.68–1.04

0.112

2082.9

  

0.88

0.59–1.32

0.531

 
 

Dominant

0.85

0.69–1.04

0.11

2080.9

 

Recessive

0.95

0.64–1.40

0.78

2083.4

 

Overdominant

0.85

0.70–1.05

0.14

2081.3

 

Log-additive

0.89

0.76–1.05

0.16

2081.5

rs2082940

Codominant

0.81

0.66–1.00

0.056

2078.1

  

0.76

0.51–1.13

0.179

 
 

Dominant

0.80

0.66–0.99

0.035

2076.2

 

Recessive

0.83

0.57–1.23

0.360

2079.8

 

Overdominant

0.84

0.68–1.03

0.1

2077.9

 

Log-additive

0.84

0.72–0.99

0.04

2076.4

  1. OR odds ratio, CI confidence interval, AIC akaike information criterion. Codominant model (homozygote for the major allele serves as the reference); Dominant model (minor allele homozygote + heterozygote vs. major allele homozygote); Recessive model (minor allele homozygote vs. major allele homozygote + heterozygote); Overdominant model (heterozygote GA vs homozygote AA + GG serve as reference); Log-additive model (compares the relative significance of the minor allele : 0,1,2 in AA, AG, and GG respectively for the G allele of rs3774261; and 0,1,2 in CC, CT, and TT respectively for the T allele of rs1063537 and rs2082940). Bold values are statistically significant.
  2. Unconditional logistic regression was used for data analyses. Age and sex, were adjusted during analyses. Bonferroni correction value =0.008 (0.05/6 = 0.008)