Genetics
Blood gene-expression signature of ITGB3, VEGFA and CETP tracks the extent of coronary artery stenosis, odds ratio 7.49 (Biochemistry (Mosc) 2025)
Original title: Expression of Preselected Genes in Mononuclear Blood Cells Is Associated with the Extent of Coronary Artery Stenosis
A study measured expression of 65 preselected HDL-metabolism and atherogenesis genes in peripheral blood mononuclear cells from 63 controls and coronary artery disease patients split into a low-stenosis group (one or two stenotic vessels, n = 35) and a high-stenosis group (three or four vessels, n = 41), confirmed by angiography. Expression of CETP, PLTP, CD36, IL18, ITGB3, S100A8, S100A12 and VEGFA rose with the number of stenotic vessels. A three-gene signature of ITGB3, VEGFA and CETP was selected as a marker of stenosis extent and validated against an independent public dataset (GSE12288), with an average odds ratio of 7.49 (95% CI, 2.21 to 25.43). The authors propose averaged expression of this signature as a candidate diagnostic and prognostic tool for coronary stenosis severity, a blood-based gene expression finding rather than a CETP inhibitor study.
Original abstract
The goal of this study was examination of the association between the expression levels of the genes involved in high-density lipoprotein metabolism and atherogenesis and underlying metabolic pathways and the number of stenotic coronary arteries. Expression of 65 preselected genes in the peripheral blood mononuclear cells of the control patients (n = 63) and patients with coronary artery disease (CAD) with one or two (low stenosis group, n = 35) or three or four (high stenosis group, n = 41) stenotic vessels, confirmed by coronary angiography, was measured with real-time PCR. Functional enrichment analysis was applied for annotation of differentially expressed genes. Protein products of the differentially expressed genes (DEGs) in the CAD patients compared to the controls were associated with metabolic pathways related to assembly, remodeling, and clearance of plasma lipoproteins, as well as with signaling and regulation of expression of the genes involved in cholesterol transport and efflux. However, comparison of the gene expression profiles and associated metabolic pathways between the groups with high versus low stenosis revealed specific differences between these groups. Expression of the CETP, PLTP, CD36, IL18, ITGB3, S100A8, S100A12, and VEGFA genes increased with the increase of the number of stenotic vessels, which suggests involvement of these genes in stenosis expansion via lipoprotein metabolism, inflammation, angiogenesis, and innate immunity. The set of genes ITGB3, VEGFA, and CETP was selected as a new gene expression signature of expansion of the coronary artery stenosis, which was validated with the GSE12288 dataset from the Gene Expression Omnibus database, demonstrating an average odds ratio (OR) of 7.49 (95% CI, 2.21 to 25.43). Averaged expression levels of the ITGB3, VEGFA, and CETP genes could be used for diagnosis, prognosis evaluation, and treatment of coronary stenosis with strong predictive power.
Summary written by cetpinhibition.org from the published abstract; figures as published. Page updated 18 August 2026. Methods.