Plasma tissue plasminogen activator and plasminogen activator inhibitor-1 in hospitalized COVID-19 patients.
Adult
Aged
Aged, 80 and over
Biomarkers
/ blood
COVID-19
/ diagnosis
Case-Control Studies
Female
Fibrin Fibrinogen Degradation Products
/ analysis
Fibrinolysis
Hospitalization
Humans
Leukocyte Count
Leukocyte L1 Antigen Complex
/ analysis
Male
Middle Aged
Neutrophils
/ cytology
Plasminogen Activator Inhibitor 1
/ blood
SARS-CoV-2
/ isolation & purification
Severity of Illness Index
Tissue Plasminogen Activator
/ blood
Journal
Scientific reports
ISSN: 2045-2322
Titre abrégé: Sci Rep
Pays: England
ID NLM: 101563288
Informations de publication
Date de publication:
15 01 2021
15 01 2021
Historique:
received:
23
10
2020
accepted:
14
12
2020
entrez:
16
1
2021
pubmed:
17
1
2021
medline:
29
1
2021
Statut:
epublish
Résumé
Patients with coronavirus disease-19 (COVID-19) are at high risk for thrombotic arterial and venous occlusions. However, bleeding complications have also been observed in some patients. Understanding the balance between coagulation and fibrinolysis will help inform optimal approaches to thrombosis prophylaxis and potential utility of fibrinolytic-targeted therapies. 118 hospitalized COVID-19 patients and 30 healthy controls were included in the study. We measured plasma antigen levels of tissue-type plasminogen activator (tPA) and plasminogen activator inhibitor-1 (PAI-1) and performed spontaneous clot-lysis assays. We found markedly elevated tPA and PAI-1 levels in patients hospitalized with COVID-19. Both factors demonstrated strong correlations with neutrophil counts and markers of neutrophil activation. High levels of tPA and PAI-1 were associated with worse respiratory status. High levels of tPA, in particular, were strongly correlated with mortality and a significant enhancement in spontaneous ex vivo clot-lysis. While both tPA and PAI-1 are elevated among COVID-19 patients, extremely high levels of tPA enhance spontaneous fibrinolysis and are significantly associated with mortality in some patients. These data indicate that fibrinolytic homeostasis in COVID-19 is complex with a subset of patients expressing a balance of factors that may favor fibrinolysis. Further study of tPA as a biomarker is warranted.
Identifiants
pubmed: 33452298
doi: 10.1038/s41598-020-80010-z
pii: 10.1038/s41598-020-80010-z
pmc: PMC7810990
doi:
Substances chimiques
Biomarkers
0
Fibrin Fibrinogen Degradation Products
0
Leukocyte L1 Antigen Complex
0
Plasminogen Activator Inhibitor 1
0
fibrin fragment D
0
Tissue Plasminogen Activator
EC 3.4.21.68
Types de publication
Journal Article
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
1580Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL115138
Pays : United States
Organisme : NHLBI NIH HHS
ID : K08 HL131993
Pays : United States
Organisme : NHLBI NIH HHS
ID : HL115138
Pays : United States
Organisme : NHLBI NIH HHS
ID : HL055374
Pays : United States
Organisme : NHLBI NIH HHS
ID : HL131993
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL150392
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL055374
Pays : United States
Commentaires et corrections
Type : UpdateOf
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