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Functional profiling prioritizes 31 CAD GWAS candidate genes in diseased vascular cells.
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Recent genome-wide association studies (GWAS) have identified 35 loci that significantly associate with coronary artery disease (CAD) susceptibility. The majority of the genes represented in these loci have not previously been studied in the context of atherosclerosis. To characterize the roles of these candidate genes in the vessel wall, we determined their expression levels in endothelial, smooth muscle, and macrophage cells isolated from healthy, prelesioned, and lesioned mouse aortas. We also performed expression quantitative locus (eQTL) mapping of these genes in human endothelial cells under control and proatherogenic conditions. Of the 57 genes studied, 31 were differentially expressed in one or more cell types in disease state in mice, and the expression levels of 8 were significantly associated with the CAD SNPs in human cells, 7 of which were also differentially expressed in mice. By integrating human and mouse results, we predict that PPAP2B, GALNT4, MAPKAPK5, TCTN1, SRR, SNF8, and ICAM1 play a causal role in the susceptibility to atherosclerosis through a role in the vasculature. Additionally, we highlight the genetic complexity of a subset of CAD loci through the differential expression of multiple candidate genes per locus and the involvement of genes that lie outside linkage disequilibrium blocks.
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Erbilgin et al. (2013) studied Coronary artery disease and atherosclerosis. CAD-associated GWAS candidate genes and SNPs vs. Healthy/control vascular cells was evaluated on Differential gene expression in mouse vascular cells and eQTL association in human endothelial cells. Expression profiling of 57 CAD GWAS candidate genes found 31 differentially expressed in diseased mouse vascular cells and 8 associated with CAD SNPs in human endothelial cells.
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