Circulating microparticles and activated platelets as novel prognostic biomarkers in COVID-19; relation to cancer

PLoS One. 2021 Feb 22;16(2):e0246806. doi: 10.1371/journal.pone.0246806. eCollection 2021.

Abstract

Background and aim: The study aimed to determine whether the MPs levels and platelet activation are affected by the COVID-19 infection in both malignant and non-malignant patients compared to healthy individuals and define their contribution to the COVID-19 associated coagulopathy and the relation of these MPs to other hematologic parameters.

Patients and methods: We recruited 23 malignant patients with reverse transcription polymerase chain reaction (RT-PCR) positive COVID-19, also, 19 COVID-19 non-malignant patients, and 20 healthy volunteers were also enrolled for comparison. Blood samples were collected from patients and healthy donors into 5 mL vacutainer tube containing 3.5% buffered sodium citrate solution for measurement of total microparticles (TMPs), platelet microparticles (PMPs), endothelial microparticles (EMPs), CD62 activated platelets, and CD41 platelet marker.

Results: COVID-19 malignant patients had significantly lower hemoglobin and platelets compared to COVID non-malignant ones, while they had significantly higher C-reactive protein, LDH, AST, Albunim, creatinine, and prognostic index (PI) compared to COVID-19 non-malignant patients. significant accumulations of TMPs, PMPs, EMPs, and activated platelets in COVID-19 affected patients compared to healthy controls. TMPs, and EMPs were significantly accumulated in COVID-19 malignant compared to COVID-19 non-malignant patients with no significant difference in PMPs between both.

Conclusion: Circulating MPs and activated platelets may be promising novel prognostic biomarkers capable of identifying potentially severe COVID-19 patients who require immediate care especially in cancer patients.

MeSH terms

  • Adult
  • Biomarkers / blood
  • Blood Coagulation
  • Blood Platelets / cytology*
  • COVID-19 / blood
  • COVID-19 / diagnosis*
  • Cell-Derived Microparticles / metabolism*
  • Female
  • Hemoglobins / analysis
  • Humans
  • Male
  • Middle Aged
  • Neoplasms / epidemiology*
  • Platelet Activation*
  • Prognosis

Substances

  • Biomarkers
  • Hemoglobins

Grant support

The authors received no specific funding for this work.