Why the study?
Does genetic variation in the ADIPOR2 gene associate with coronary artery disease and markers of atherosclerosis in patients with cardiovascular risk factors?
Does genetic variation in the ADIPOR2 gene associate with coronary artery disease and markers of atherosclerosis in patients with cardiovascular risk factors?
Variants of the ADIPOR2 gene, specifically the rs767870 polymorphism, are associated with coronary artery disease, increased intima-media thickness, and reduced flow-mediated dilatation, independent of insulin resistance.
Answers are grounded in this paper and cite their sources.
ADIPOR2 rs767870 variation does not yet warrant genetic testing; leaves open its causal role in atherosclerosis beyond observational association.
BACKGROUND: Adiponectin is an adipose tissue secreted protein known for its insulin sensitising and anti-atherogenic actions. To this date two adiponectin receptors have been discovered, adiponectin receptor 1 (ADIPOR1) and adiponectin receptor 2 (ADIPOR2). The aim of this study was to investigate the association of ADIPOR2 gene variations with coronary artery disease (CAD). METHODS: Eight common single nucleotide polymorphisms (SNPs) spanning the entire ADIPOR2 locus were chosen to perform association studies with anthropometric and metabolic parameters in a Greek population. They were classified as either CAD (stenosis >50% in at least one main vessel) or non-CAD individuals in accordance with coronary angiography data.Genotyping was performed using a microsphere-based suspension array and the Allele Specific Primer Extension (ASPE) method. Expression of ADIPOR2 protein and mRNA in circulating CD14+ monocytes were determined using flow cytometry and real time Polymerase Chain Reaction assays respectively. RESULTS: There was a significant difference in the distribution of genotypes of polymorphism rs767870 of ADIPOR2 between CAD and non-CAD individuals (p = 0.017). Furthermore, heterozygotes of the rs767870 polymorphism had significantly lower Flow Mediated Dilatation (FMD) values, higher values of Intima-Media Thickness (IMT) and increased ADIPOR2 protein levels in peripheral monocytes, compared to homozygotes of the minor allele after adjustment for age, sex, waist to hip ratio and HOMA. CONCLUSIONS: Our findings suggest that variants of ADIPOR2 could be a determinant for atherosclerosis independent of insulin resistance status, possibly by affecting ADIPOR2 protein levels.
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Halvatsiotis et al. (2010) studied this question.
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