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Published on: August 9, 2024
Non-invasive gene-expression-based detection of well-developed collateral function in individuals with and without
P Meier1, J Antonov, R Zbinden
1Department of Cardiology, University Hospital, Freiburgstrasse, Bern, Switzerland.
Insights
Gene expression in blood monocytes can identify coronary collateral circulation status. This finding may lead to non-invasive diagnostics for coronary artery disease patients, highlighting MCP-1
Area of Science:
- Cardiovascular Biology
- Molecular Genetics
- Immunology
Background:
- Coronary artery disease (CAD) patients benefit from well-developed collateral circulation.
- Identifying genetic markers for coronary collateral circulation is crucial for understanding disease progression.
Purpose of the Study:
- To identify marker genes in peripheral blood monocytes associated with extensively grown coronary collateral circulation.
- To explore the role of MCP-1 in regulating genes involved in collateral formation.
Main Methods:
- Invasive Collateral Flow Index (CFI) measurement in 160 individuals.
- Microarray and real-time PCR for gene expression analysis in monocytes.
- Receiver operating characteristics analysis for differentiating collateral status.
Main Results:
- Significant correlation between gene expression and CFI in CAD patients and controls.
- Identified 76 genes in four key signaling pathways: angiogenesis, integrin, PDGF, and TGF-beta.
- Three genes per subgroup showed high specificity in differentiating low vs. high CFI; two were affected by MCP-1 stimulation.
Conclusions:
- Genetic factors are integral to coronary collateral circulation development.
- Gene expression profiling of monocytes offers a non-invasive method to assess collateralization.
- MCP-1 influences monocyte arteriogenic potential, impacting collateral formation.
Background:
In patients with coronary artery disease (CAD), a well grown collateral circulation has been shown to be important. The aim of this prospective study using peripheral blood monocytes was to identify marker genes for an extensively grown coronary collateral circulation.
Methods:
Collateral flow index (CFI) was obtained invasively by angioplasty pressure sensor guidewire in 160 individuals (110 patients with CAD, and 50 individuals without CAD). RNA was extracted from monocytes followed by microarray-based gene-expression analysis. 76 selected genes were analysed by real-time polymerase chain reaction (PCR). A receiver operating characteristics analysis based on differential gene expression was then performed to separate individuals with poor (CFI<0.21) and well-developed collaterals (CFI>or=0.21) Thereafter, the influence of the chemokine MCP-1 on the expression of six selected genes was tested by PCR.
Results:
The expression of 203 genes significantly correlated with CFI (p = 0.000002-0.00267) in patients with CAD and 56 genes in individuals without CAD (p = 00079-0.0430). Biological pathway analysis revealed 76 of those genes belonging to four different pathways: angiogenesis, integrin-, platelet-derived growth factor-, and transforming growth factor beta-signalling. Three genes in each subgroup differentiated with high specificity among individuals with low and high CFI (>or=0.21). Two out of these genes showed pronounced differential expression between the two groups after cell stimulation with MCP-1.
Conclusions:
Genetic factors play a role in the formation and the preformation of the coronary collateral circulation. Gene expression analysis in peripheral blood monocytes can be used for non-invasive differentiation between individuals with poorly and with well grown collaterals. MCP-1 can influence the arteriogenic potential of monocytes.
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