SARS-COV-2 causes significant abnormalities in the fibrinolysis system of patients: correlation between viral mutations, variants and thrombosis

  • 0Department of Botany and Microbiology, College of Science, King Saud University, Riyadh, Saudi Arabia.

Summary

This summary is machine-generated.

Specific SARS-CoV-2 mutations correlate with severe COVID-19 outcomes and thrombosis risk. Understanding these genetic links is crucial for managing coagulopathy and improving patient care during the pandemic.

Area Of Science

  • Virology
  • Hematology
  • Genetics

Background

  • Coronavirus disease (COVID-19) is a complex, multi-system disorder associated with coagulopathy and mortality.
  • Investigating the link between SARS-CoV-2 genetic variations and coagulation system changes is vital for understanding disease severity.

Purpose Of The Study

  • To investigate the correlation between SARS-CoV-2 mutations in blood samples and changes in the fibrinolysis system.
  • To assess the relationship between these mutations, disease severity, and intensive care unit (ICU) admission.

Main Methods

  • Recruited 446 COVID-19 patients between 2021-2022.
  • Performed sequence analysis of the SARS-CoV-2 spike gene from blood samples.
  • Measured fibrinolysis and coagulation parameters including D-dimer, fibrinogen, tPA, and PAI-1.

Main Results

  • SARS-CoV-2 RNA detected in 27.6% of blood samples.
  • Specific mutations (N501Y, D614G, K417N, P681R) linked to increased ICU admissions.
  • Omicron (BA.1.1) variant associated with thrombosis in unvaccinated, comorbid patients.
  • N501Y mutation correlated with elevated tPA, aPTT, and D-dimer levels.

Conclusions

  • Thrombosis is a prevalent complication in severe COVID-19.
  • Further research is needed to understand the link between SARS-CoV-2 variants and thrombosis development.

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