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Updated: Sep 26, 2026

Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Prothrombotic response to coronary angioplasty in patients with unstable angina and raised C-reactive protein
Alessandro Sciahbasi1, Felicita Andreotti, Raimondo De Cristofaro
1Institute of Cardiology, Catholic University, Rome, Italy.
Insights
High C-reactive protein (CRP) levels before coronary angioplasty predict increased von Willebrand factor (vWF) and platelet reactivity in unstable angina patients. These inflammatory markers may explain worse outcomes in unstable patients.
Area of Science:
- Cardiovascular Medicine
- Inflammation Research
- Hemostasis and Thrombosis
Background:
- C-reactive protein (CRP) is linked to coronary thrombosis risk.
- Mechanisms connecting inflammation and hemostasis in coronary angioplasty require elucidation.
Purpose of the Study:
- Investigate the relationship between inflammatory state and hemostatic response post-coronary angioplasty.
- Determine if preprocedural C-reactive protein levels predict changes in hemostatic markers.
Main Methods:
- Measured plasma levels of vWF antigen, vWF collagen binding activity, vWF-cleaving-protease, CRP, and platelet reactivity before and after angioplasty.
- Stratified 35 patients (18 unstable, 17 stable angina) by preprocedural CRP levels (<3 mg/l vs. >=3 mg/l).
Main Results:
- Patients with unstable angina and high preprocedural CRP showed significant increases in vWF antigen, vWF collagen-binding, CRP, and platelet reactivity post-angioplasty.
- Changes in vWF antigen and vWF collagen-binding correlated with CRP level changes post-angioplasty.
- No significant changes observed in the stable angina group or unstable angina patients with low CRP.
Conclusions:
- High preprocedural CRP levels predict a significant increase in vWF after angioplasty in unstable angina patients.
- The rise in vWF is associated with elevated CRP and enhanced platelet reactivity.
- These inflammatory and hemostatic changes may contribute to the poorer prognosis in unstable angina patients with elevated inflammation markers.
Background:
To better understand the mechanisms linking C reactive protein (CRP) to the risk of coronary thrombosis, we investigated the relation between inflammatory state and hemostatic response to coronary angioplasty in patients with either stable or unstable angina.
Methods:
Plasma levels of von Willebrand factor (vWF) antigen, vWF collagen binding activity, vWF-cleaving-protease, CRP, and whole-blood platelet reactivity were measured before and 24 h after angioplasty in 18 patients with recent unstable angina and in 17 with stable angina. Each group was divided according to preprocedural CRP levels: >or=3 mg/l (in 9 unstable and 9 stable patients) or <3 mg/l (in 9 unstable and 8 stable patients).
Results:
Baseline hemostatic parameters did not differ significantly among the four subgroups of patients. After angioplasty, virtually all patients with unstable angina and raised preprocedural CRP showed increased vWF antigen (P = 0.01), vWF collagen-binding (P = 0.001), CRP (P = 0.008), and platelet reactivity (P = 0.0007) compared to baseline, whereas no significant change of these variables was seen within the other three sets of patients. In the overall population, the changes in vWF antigen and vWF-collagen-binding induced by angioplasty correlated with those in CRP levels (r = 0.47, P = 0.004 and r = 0.44, P = 0.008). Baseline levels of vWF cleaving protease and modifications of this enzyme with angioplasty did not differ significantly among subgroups.
Conclusions:
Our data suggest that high preprocedural levels of CRP predict a significant vWF rise after angioplasty in patients with unstable angina. The rise in vWF is associated with that in CRP and with enhanced platelet reactivity. Such changes may contribute to the worse prognosis of unstable patients with raised indices of inflammation.
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