Key result
The TT genotype of the ADIPOQ +276G/T polymorphism was associated with a significantly increased risk of coronary artery disease compared to the reference GG genotype in patients with type 2 diabetes (OR 5.158).
Why the study?
Are ADIPOQ gene single nucleotide polymorphisms (+45T/G and +276G/T) associated with coronary artery disease in patients with type 2 diabetes?
Case-Control (n=200)
No
Are ADIPOQ gene single nucleotide polymorphisms (+45T/G and +276G/T) associated with coronary artery disease in patients with type 2 diabetes?
Odds Ratio: 5.158 (95% CI 1.016–26.182)
Absolute Event Rate: 7% vs 2%
p-value: p=0.048
The T allele of the ADIPOQ +276G/T SNP is associated with an increased risk of coronary artery disease in patients with type 2 diabetes, while a specific haplotype combination may be protective.
May indicate higher CAD risk in T2D; leaves open prospective validation before clinical consideration.
BACKGROUND: Adiponectin, an adipocyte-secreted hormone, is known to have anti-atherogenic, anti-inflammatory, and anti-diabetic properties. In the present study, the association between two common single nucleotide polymorphisms (SNPs) (+45T/G and +276G/T) of ADIOPQ gene and coronary artery disease (CAD) was assessed in the subjects with type 2 diabetes (T2DM). METHODS: Genotypes of two SNPs were determined by polymerase chain reaction-restriction fragment length polymorphism in 200 subjects with T2DM (100 subjects with CAD and 100 without CAD). RESULTS: The frequency of TT genotype of +276G/T was significantly elevated in CAD compared to controls (χ2=7.967, P=0.019). A similar difference was found in the allele frequency of +276G/T between two groups (χ2=3.895, P=0.048). The increased risk of CAD was associated with +276 TT genotype when compared to reference GG genotype (OR=5.158; 95% CI=1.016-26.182, P=0.048). However, no similar difference was found in genotype and allele frequencies of SNP +45T/G between two groups. There was a CAD protective haplotype combination of +276 wild-type and +45 mutant-type allele (276G-45G) (OR=0.37, 95% CI=0.16-0.86, P=0.022) in the subject population. CONCLUSION: Our findings indicated that T allele of SNP +276G/T is more associated with the increased risk of CAD in subjects with T2DM. Also, a haplotype combination of +45G/+276G of these two SNPs has a protective effect on the risk of CAD.
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Mohammadzadeh et al. (2016) conducted a case-control in Type 2 Diabetes Mellitus with or without Coronary Artery Disease (n=200). ADIPOQ +276G/T polymorphism (TT genotype) vs. GG genotype (wild-type) was evaluated on Risk of coronary artery disease (OR 5.158, 95% CI 1.016-26.182, p=0.048). The TT genotype of the ADIPOQ +276G/T polymorphism was associated with a significantly increased risk of coronary artery disease compared to the reference GG genotype in patients with type 2 diabetes (OR 5.158).
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