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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Platelet characteristics associated with coronary artery disease
R D McBane1, K Karnicki, N Tahirkheli
1Division of Cardiovascular Medicine, Section of Hematology Research, Mayo Clinic and Foundation for Education and Research, 200 S.W. First Street, Rochester, MN 55905, USA.
Insights
Platelets from patients with coronary artery disease show reduced P-selectin expression and increased microaggregation. These platelet changes may reflect systemic atherosclerosis, not just acute injury.
Area of Science:
- Cardiovascular Medicine
- Hematology
- Atherosclerosis Research
Background:
- Circulating platelets may play a role in atherogenesis.
- Platelet function markers can indicate disease activity.
Purpose of the Study:
- To investigate platelet P-selectin expression and microaggregation in patients with coronary calcification (CC) and acute coronary syndromes (AC).
- To assess the impact of angioplasty on platelet function.
Main Methods:
- Measured P-selectin expression after thrombin stimulation.
- Assessed platelet microaggregation using platelet count differences in citrate vs. EDTA anticoagulated samples.
- Collected samples before, and at 30 minutes and 24 hours after angioplasty.
Main Results:
- Platelets from AC and CC patients exhibited significantly lower P-selectin expression compared to normal donors.
- Platelets from AC and CC patients showed a greater propensity for microaggregation in citrate anticoagulant.
- Angioplasty led to a transient decrease in platelet count in platelet-rich plasma.
Conclusions:
- Both stable (CC) and unstable (AC) coronary disease are linked to altered platelet populations with reduced P-selectin expression and increased microaggregation.
- These platelet abnormalities may stem from systemic atherosclerosis or the atherogenic process, rather than solely from acute arterial injury.
Background/Objective:
To test the hypothesis that circulating platelets display evidence of interactions with atherogenesis, platelet capacity to express P-selectin and propensity for spontaneous microaggregation in vitro were measured in samples from normal donors (N), patients with asymptomatic advanced coronary calcification (CC) or acute coronary syndromes (AC). To measure the effect of angioplasty on platelet function, samples obtained before, 30 min after and 24 h after angioplasty were compared.
Patients/Methods:
Platelet P-selectin was measured after maximal stimulation with thrombin. Microaggregation was measured as a platelet count deficit in citrate-anticoagulated platelet-rich plasma (PRP) relative to EDTA-anticoagulated blood.
Results:
P-selectin expression was significantly lower for platelets from patients with either AC or CC compared to normals. In addition, platelets from AC and CC patients have a significantly greater propensity to form microaggregates in citrate anticoagulant. After angioplasty, the PRP-platelet count decreased transiently.
Conclusion:
Both acute unstable and chronic stable coronary disease are associated with an increased share of platelets unable to express P-selectin and an increased share of platelets that microaggregate in citrate anticoagulant. The genesis of these platelet characteristics is not fully explained by focal acute arterial injury and may reflect exposure to systemic atherosclerosis or the atherogenic process.
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