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10.3390/cells10010085

http://scihub22266oqcxt.onion/10.3390/cells10010085
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33430260!7825711!33430260
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suck abstract from ncbi


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pmid33430260      Cells 2021 ; 10 (1): ä
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  • Circulating Platelet-Derived Extracellular Vesicles Are a Hallmark of Sars-Cov-2 Infection #MMPMID33430260
  • Cappellano G; Raineri D; Rolla R; Giordano M; Puricelli C; Vilardo B; Manfredi M; Cantaluppi V; Sainaghi PP; Castello L; De Vita N; Scotti L; Vaschetto R; Dianzani U; Chiocchetti A
  • Cells 2021[Jan]; 10 (1): ä PMID33430260show ga
  • Sars-Cov-2 infection causes fever and cough that may rapidly lead to acute respiratory distress syndrome (ARDS). Few biomarkers have been identified but, unfortunately, these are individually poorly specific, and novel biomarkers are needed to better predict patient outcome. The aim of this study was to evaluate the diagnostic performance of circulating platelets (PLT)-derived extracellular vesicles (EVs) as biomarkers for Sars-Cov-2 infection, by setting a rapid and reliable test on unmanipulated blood samples. PLT-EVs were quantified by flow cytometry on two independent cohorts of Sars-CoV-2+ (n = 69), Sars-Cov-2- (n = 62) hospitalized patients, and healthy controls. Diagnostic performance of PLT-EVs was evaluated by receiver operating characteristic (ROC) curve. PLT-EVs count were higher in Sars-Cov-2+ compared to Sars-Cov-2- patients or HC. ROC analysis of the combined cohorts showed an AUC = 0.79 and an optimal cut-off value of 1472 EVs/muL, with 75% sensitivity and 74% specificity. These data suggest that PLT-EVs might be an interesting biomarker deserving further investigations to test their predictive power.
  • |Aged[MESH]
  • |Aged, 80 and over[MESH]
  • |Biomarkers/blood[MESH]
  • |Blood Platelets/*metabolism/pathology[MESH]
  • |COVID-19/*blood/epidemiology[MESH]
  • |Case-Control Studies[MESH]
  • |Cohort Studies[MESH]
  • |Extracellular Vesicles/*metabolism[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]


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