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Isolation of Perivascular Multipotent Precursor Cell Populations from Human Cardiac Tissue
Published on: October 8, 2016
Circulating cell adhesion molecules and death in patients with coronary artery disease
S Blankenberg1, H J Rupprecht, C Bickel
1Department of Medicine II, Johannes Gutenberg-University Mainz, Germany. stefan.blankenberg@uni-mainz.de
Insights
Higher levels of soluble adhesion molecules, including vascular cell adhesion molecule-1 (sVCAM-1), predict future cardiovascular death in coronary artery disease (CAD) patients. Soluble VCAM-1 is a significant independent predictor of fatal cardiovascular events.
Area of Science:
- Cardiovascular Medicine
- Immunology
- Biomarkers
Background:
- Leukocyte adhesion molecules like VCAM-1, ICAM-1, and E-selectin contribute to atherosclerosis progression.
- These molecules mediate leukocyte adhesion and transmigration, potentially driving plaque instability.
Purpose of the Study:
- To investigate the association between soluble adhesion molecules and future cardiovascular events in patients with coronary artery disease (CAD).
- To determine if soluble adhesion molecules improve risk prediction beyond established factors.
Main Methods:
- Prospective cohort study of 1246 patients with angiographically documented CAD.
- Baseline measurement of soluble VCAM-1 (sVCAM-1), sICAM-1, and sE-selectin.
- Follow-up for cardiovascular events over a mean of 2.7 years.
Main Results:
- Elevated sVCAM-1, sICAM-1, and sE-selectin levels were associated with increased cardiovascular death.
- Patients in the highest quartile of sVCAM-1 had a 2.1-fold higher risk of fatal events.
- sVCAM-1 remained an independent predictor of cardiovascular death, even after accounting for inflammation markers like hs-CRP.
Conclusions:
- Soluble adhesion molecules, particularly sVCAM-1, are significantly linked to future cardiovascular mortality in CAD patients.
- sVCAM-1 enhances the predictive value of traditional risk factors and hs-CRP for cardiovascular death.
Background:
Vascular cell adhesion molecule (VCAM)-1, intercellular adhesion molecule (ICAM)-1, and E-selectin mediate adhesion and transmigration of leukocytes to the vascular endothelial wall and may promote plaque growth and instability. In a prospective study, we evaluated the effect of soluble adhesion molecules on the risk of future cardiovascular events among patients with angiographically documented coronary artery disease (CAD). Methods and Results- -We obtained baseline samples from a prospective cohort of 1246 patients with CAD. Besides various markers of inflammation, soluble VCAM-1 (sVCAM-1), sICAM-1, and sE-selectin were determined. Follow-up information on cardiovascular events was obtained (mean, 2.7; maximum, 4.1 years). Independently higher levels of sVCAM-1 (1932 versus 1128 ng/mL; P<0.0001), sICAM-1 (353 versus 287 ng/mL; P=0.015), and sE-selectin (81 versus 63 ng/mL; P=0.003) were observed in patients with future death from cardiovascular causes. In a multivariate model, fatal risk was 2.1-fold (1.1 to 4.0) higher in patients within the top quartile of baseline sVCAM-1 concentrations compared with lower quartiles. This association was present independent of general inflammatory response as reflected by low or high C-reactive protein (hs-CRP) levels. In a model that simultaneously controlled for all inflammatory and soluble adhesion markers determined, only sVCAM-1 remained independently significant for future fatal cardiovascular events, with a 2.8-fold increase in risk (P=0.003).
Conclusions:
Soluble adhesion molecules sVCAM-1, sICAM-1, and sE-selectin were significantly related to future death from cardiovascular causes among patients with documented CAD. Especially sVCAM-1 added to the predictive value of classic risk factors and hs-CRP in determining the risk of future cardiovascular death.
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