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Updated: Aug 3, 2025

Author Spotlight: Integrated Multi-Omics Analysis for Unveiling Multicellular Immune Signatures in Clinical Heart Attack Cohorts
Published on: September 20, 2024
Targeted Blood Plasma Proteomics and Hemostasis Assessment of Post COVID-19 Patients with Acute Myocardial Infarction
Anna Kalinskaya1,2, Daria Vorobyeva1,2, George Rusakovich2
1Laboratory of Atherothrombosis, Cardiology Department, A.I. Evdokimov Moscow State University of Medicine and Dentistry, 127473 Moscow, Russia.
Insights
Cardiovascular complications after SARS-CoV-2 infection are linked to altered blood clotting and inflammation. COVID-19 survivors with acute myocardial infarction show distinct protein profiles, suggesting prolonged immune changes.
Area of Science:
- Cardiovascular Medicine
- Infectious Diseases
- Hematology
Background:
- The molecular basis of cardiovascular complications post-SARS-CoV-2 infection is not fully understood.
- Acute myocardial infarction (AMI) is a known complication, but its association with prior COVID-19 requires further investigation.
Purpose of the Study:
- To investigate blood coagulation, platelet aggregation, and plasma proteomic profiles in COVID-19 convalescents with AMI.
- To compare these features between patients with AMI post-COVID, AMI without COVID-19, and healthy controls with or without COVID-19 history.
Main Methods:
- Rotational thromboelastometry, thrombodynamics, and impedance aggregometry were used to assess hemostasis.
- Plasma proteomics analysis was performed to identify differential protein expression.
- Participants were stratified based on anti-N IgG levels for SARS-CoV-2 infection.
Main Results:
- Both AMI groups exhibited increased clot growth rates, thrombus size/density, and elevated levels of complement, endothelium-modifying, acute-phase, and procoagulant proteins.
- AMI patients post-COVID showed reduced levels of inflammation and hemostasis-related proteins (e.g., LBP, C4b-BPα, C1 inhibitor, fibrinogen β, protein S) compared to AMI controls.
- A less pronounced increase in acute-phase and hemostatic markers was observed in AMI post-COVID patients, potentially due to persistent immune alterations.
Conclusions:
- COVID-19 convalescence is associated with distinct hemostatic and proteomic alterations in patients with AMI.
- These findings suggest that prolonged immune system dysregulation after COVID-19 may influence cardiovascular complication development.
- Further research is needed to elucidate the long-term cardiovascular sequelae of SARS-CoV-2 infection.
Abstract:
The molecular mechanisms underlying cardiovascular complications after the SARS-CoV-2 infection remain unknown. The goal of our study was to analyze the features of blood coagulation, platelet aggregation, and plasma proteomics in COVID-19 convalescents with AMI. The study included 66 AMI patients and 58 healthy volunteers. The groups were divided according to the anti-N IgG levels (AMI post-COVID (n = 44), AMI control (n = 22), control post-COVID (n = 31), and control (n = 27)). All participants underwent rotational thromboelastometry, thrombodynamics, impedance aggregometry, and blood plasma proteomics analysis. Both AMI groups of patients demonstrated higher values of clot growth rates, thrombus size and density, as well as the elevated levels of components of the complement system, proteins modifying the state of endothelium, acute-phase and procoagulant proteins. In comparison with AMI control, AMI post-COVID patients demonstrated decreased levels of proteins connected to inflammation and hemostasis (lipopolysaccharide-binding protein, C4b-binding protein alpha-chain, plasma protease C1 inhibitor, fibrinogen beta-chain, vitamin K-dependent protein S), and altered correlations between inflammation and fibrinolysis. A new finding is that AMI post-COVID patients opposite the AMI control group, are characterized by a less noticeable growth of acute-phase proteins and hemostatic markers that could be explained by prolonged immune system alteration after COVID-19.
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