Soluble Urokinase Plasminogen Activator Receptor and Venous Thromboembolism in COVID-19.
COVID‐19
soluble urokinase plasminogen activator receptor
thromboembolism
Journal
Journal of the American Heart Association
ISSN: 2047-9980
Titre abrégé: J Am Heart Assoc
Pays: England
ID NLM: 101580524
Informations de publication
Date de publication:
20 09 2022
20 09 2022
Historique:
pubmed:
5
8
2022
medline:
23
9
2022
entrez:
4
8
2022
Statut:
ppublish
Résumé
Background Venous thromboembolism (VTE) contributes significantly to COVID-19 morbidity and mortality. The urokinase receptor system is involved in the regulation of coagulation. Levels of soluble urokinase plasminogen activator receptor (suPAR) reflect hyperinflammation and are strongly predictive of outcomes in COVID-19. Whether suPAR levels identify patients with COVID-19 at risk for VTE is unclear. Methods and Results We leveraged a multinational observational study of patients hospitalized for COVID-19 with suPAR and D-dimer levels measured on admission. In 1960 patients (mean age, 58 years; 57% men; 20% Black race), we assessed the association between suPAR and incident VTE (defined as pulmonary embolism or deep vein thrombosis) using logistic regression and Fine-Gray modeling, accounting for the competing risk of death. VTE occurred in 163 (8%) patients and was associated with higher suPAR and D-dimer levels. There was a positive association between suPAR and D-dimer (β=7.34;
Identifiants
pubmed: 35924778
doi: 10.1161/JAHA.122.025198
pmc: PMC9683642
doi:
Substances chimiques
Biomarkers
0
Receptors, Urokinase Plasminogen Activator
0
Urokinase-Type Plasminogen Activator
EC 3.4.21.73
Banques de données
ClinicalTrials.gov
['NCT04818866']
Types de publication
Journal Article
Observational Study
Research Support, N.I.H., Extramural
Research Support, Non-U.S. Gov't
Langues
eng
Sous-ensembles de citation
IM
Pagination
e025198Subventions
Organisme : NHLBI NIH HHS
ID : R01 HL153384
Pays : United States
Organisme : NHLBI NIH HHS
ID : T32 HL007853
Pays : United States
Organisme : NIDDK NIH HHS
ID : U01 DK119083
Pays : United States
Organisme : NIDDK NIH HHS
ID : U2C DK110768
Pays : United States
Investigateurs
Salim S Hayek
(SS)
Pennelope Blakely
(P)
Christopher Launius
(C)
Hanna Berlin
(H)
Kingsley Amadi
(K)
Tariq U Azam
(TU)
Husam Shadid
(H)
Michael Pan
(M)
Patrick O'Hayer
(P)
Chelsea Meloche
(C)
Rafey Feroze
(R)
Kishan J Padalia
(KJ)
Elizabeth Anderson
(E)
Danny Perry
(D)
Abbas Bitar
(A)
Rayan Kaakati
(R)
Lili Zhao
(L)
Peiyao Zhao
(P)
Erinleigh Michaud
(E)
Yiyuan Huang
(Y)
Toniemarie Catalan
(T)
Ibrahim Khaleel
(I)
Jochen Reiser
(J)
Beata Samelko
(B)
Alexander Hlepas
(A)
Xuexiang Wang
(X)
Priya Patel
(P)
Jesper Eugen-Olsen
(J)
Izzet Altintas
(I)
Jens Tingleff
(J)
Marius Stauning
(M)
Morten Baltzer Houlind
(MB)
Mette B Lindstrøm
(MB)
Ove Andersen
(O)
Hejdi Gamst-Jensen
(H)
Line Jee Hartmann Rasmussen
(LJH)
Christian Rasmussen
(C)
Jan O Nehlin
(JO)
Thomas Kallemose
(T)
Imran Parvaiz
(I)
Evangelos J Giamarellos-Bourboulis
(EJ)
Maria-Evangelia Adami
(ME)
Nicky Solomonidi
(N)
Maria Tsilika
(M)
Maria Saridaki
(M)
Vasileios Lekakis
(V)
Sven Loosen
(S)
Tom Luedde
(T)
Verena Keitel
(V)
Athanasios Chalkias
(A)
Ioannis Pantazopoulos
(I)
Eleni Laou
(E)
Anargyros Skoulakis
(A)
Frank Tacke
(F)
Pinkus Tober-Lau
(P)
Raphael Mohr
(R)
Florian Kurth
(F)
Leif Erik Sander
(LE)
Christoph Jochum
(C)
Philipp Koehler
(P)
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