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Coronary Progenitor Cells and Soluble Biomarkers in Cardiovascular Prognosis after Coronary Angioplasty
Published on: January 28, 2020
Long-term prognostic value of protein C activity, erythrocyte aggregation and membrane fluidity in transmural
Luis Sargento1, Carlota Saldanha, José Monteiro
1Instituto de Bioquímica, Unidade de Biopatologia Vascular-IMM, Faculdade de Medicina de Lisboa, Portugal. Luis.sargento@netcabo.pt
Insights
Disturbances in blood clotting, flow, and inflammation after myocardial infarction (MI) predict future cardiovascular events. Monitoring these factors at discharge can identify high-risk patients for long-term management.
Area of Science:
- Cardiology
- Hematology
- Biochemistry
Background:
- Transmural myocardial infarction (MI) survivors face risks of recurrent cardiovascular events.
- Identifying long-term predictors of these events is crucial for patient management.
- Haemostatic, inflammatory, and haemorheologic factors are implicated in cardiovascular disease.
Purpose of the Study:
- To evaluate the long-term predictive value of haemostatic, inflammatory, and haemorheologic disturbances in survivors of transmural MI.
- To determine if specific biomarkers at hospital discharge can predict future cardiovascular events.
Main Methods:
- Sixty-four MI survivors were followed for 36 months.
- Haemostatic (protein C activity, antithrombin III, PAI-1), haemorheologic (blood fluidity, erythrocyte membrane fluidity), and inflammatory (elastase, leukocyte count) profiles were assessed at discharge.
- Cox regression analysis was used to identify independent predictors of cardiovascular events.
Main Results:
- Patients who experienced subsequent cardiovascular events had higher leukoactivity, leukocyte count, and membrane fluidity, but lower protein C activity and erythrocyte aggregation at discharge.
- Lower protein C activity, higher erythrocyte membrane outer layer fluidity, and lower erythrocyte aggregation were identified as independent predictors of the composite endpoint.
- These factors demonstrated significant predictive value in Cox regression analysis.
Conclusions:
- Haemostatic, haemorheologic, and inflammatory disturbances at hospital discharge are significant long-term predictors of recurrent cardiovascular events in MI survivors.
- These findings highlight the potential for using these biomarkers to stratify risk and guide therapeutic strategies.
Abstract:
The objective of this study was to evaluate the long-term predictive value of the haemostatic, inflammatory and haemorheologic disturbances in transmural myocardial infarction (MI). Sixty-four (59 male) consecutive survivors of a MI, with a mean age of 58.3 +/- 12.0 years, were followed over a period of 36 months. Eighteen patients had a cardiovascular event defined as the composite of death, non-fatal MI, unstable angina and stroke. The haemostatic (protein C activity-PtC, antithrombin III, plasminogen activator inhibitor-1), haemorheologic (blood fluidity and components, erythrocyte membrane fluidity) and inflammatory (polymorphonuclear elastase, leukocyte count) profiles were determined at hospital discharge, using standard methodology. Our results can be summarized as follow: (i) at hospital discharge, the subgroup of patients with events had higher leukoactivity, leukocyte count, membrane fluidity, prognosis cyte count (7833.0 +/- 1696.0 vs. 10294.0 +/- 3129.0; p = 0.011), lower PtC (100.65 +/- 19.08 vs.81.25 +/- 19.95; p = 0.002), and lower erythrocyte aggregation (14.26 +/- 5.94 vs. 11.47 +/- 3.45; p = 0.031) in relation to the ones without events; (ii) By Cox regression the protein C activity lower tertile (OR 0.169; 0.045-0.628; p = 0.008); erythrocyte membrane outer layer fluidity upper tertile (OR 0.067; 95% CI 0.011 - 0.393; p = 0.003); and erythrocyte aggregation lower tertile (OR 0.182; 0.038 - 0.876; p = 0.034) were independent predictors of the composite endpoint. We can conclude that some haemostatic, haemorheologic and inflammatory disturbances, at hospital discharge, are long-term independent predictors of recurrent cardiovascular events in transmural myocardial infarction survivors.
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