Soluble Urokinase Plasminogen Activator Receptor and Venous Thromboembolism in COVID‐19

Author:

Luo Shengyuan1ORCID,Vasbinder Alexi2,Du‐Fay‐de‐Lavallaz Jeanne M.3,Gomez Joanne Michelle D.4,Suboc Tisha1,Anderson Elizabeth2,Tekumulla Annika2ORCID,Shadid Husam5,Berlin Hanna5ORCID,Pan Michael5,Azam Tariq U.2ORCID,Khaleel Ibrahim5,Padalia Kishan5,Meloche Chelsea5,O'Hayer Patrick5,Catalan Tonimarie2,Blakely Pennelope2ORCID,Launius Christopher2,Amadi Kingsley‐Michael2,Pop‐Busui Rodica6,Loosen Sven H.7,Chalkias Athanasios89ORCID,Tacke Frank10,Giamarellos‐Bourboulis Evangelos J.11ORCID,Altintas Izzet12,Eugen‐Olsen Jesper12ORCID,Williams Kim A.13,Volgman Annabelle Santos1ORCID,Reiser Jochen1,Hayek Salim S.2ORCID,Hayek Salim S.,Blakely Pennelope,Launius Christopher,Berlin Hanna,Amadi Kingsley,Azam Tariq U.,Shadid Husam,Pan Michael,O’Hayer Patrick,Meloche Chelsea,Feroze Rafey,Padalia Kishan J.,Anderson Elizabeth,Perry Danny,Bitar Abbas,Kaakati Rayan,Zhao Lili,Zhao Peiyao,Michaud Erinleigh,Huang Yiyuan,Catalan Toniemarie,Khaleel Ibrahim,Reiser Jochen,Samelko Beata,Hlepas Alexander,Wang Xuexiang,Patel Priya,Eugen‐Olsen Jesper,Altintas Izzet,Tingleff Jens,Stauning Marius,Houlind Morten Baltzer,Lindstrøm Mette B.,Andersen Ove,Gamst‐Jensen Hejdi,Rasmussen Line Jee Hartmann,Rasmussen Christian,Nehlin Jan O.,Kallemose Thomas,Parvaiz Imran,Giamarellos‐Bourboulis Evangelos J.,Adami Maria‐Evangelia,Solomonidi Nicky,Tsilika Maria,Saridaki Maria,Lekakis Vasileios,Loosen Sven,Luedde Tom,Keitel Verena,Chalkias Athanasios,Pantazopoulos Ioannis,Laou Eleni,Skoulakis Anargyros,Tacke Frank,Tober‐Lau Pinkus,Mohr Raphael,Kurth Florian,Sander Leif Erik,Jochum Christoph,Koehler Philipp

Affiliation:

1. Department of Medicine Rush University Medical Center Chicago IL

2. Division of Cardiology, Department of Internal Medicine University of Michigan Ann Arbor MI

3. Department of Medicine University Hospital Basel Basel Switzerland

4. Division of Cardiology Smidt Heart Institute, Cedars Sinai Medical Center Los Angeles CA

5. Department of Internal Medicine University of Michigan Ann Arbor MI

6. Division of Metabolism, Endocrinology and Diabetes, Department of Internal Medicine University of Michigan Ann Arbor MI

7. Clinic for Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty University Hospital Düsseldorf Düsseldorf Germany

8. Department of Anesthesiology, Faculty of Medicine University of Thessaly Larisa Greece

9. Outcomes Research Consortium Cleveland OH

10. Department of Hepatology and Gastroenterology, Campus Charité Mitte and Campus Virchow‐Klinikum Charité University Medicine Berlin Berlin Germany

11. 4th Department of Internal Medicine National and Kapodistrian University of Athens Athens Greece

12. Department of Clinical Research Copenhagen University Hospital Hvidovre Hvidovre Denmark

13. Department of Internal Medicine University of Louisville School of Medicine Louisville KY

Abstract

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; P =0.002). Adjusted for clinical covariables, including D‐dimer, the odds of VTE were 168% higher comparing the third with first suPAR tertiles (adjusted odds ratio, 2.68 [95% CI, 1.51–4.75]; P <0.001). Findings were consistent when stratified by D‐dimer levels and in survival analysis accounting for death as a competing risk. On the basis of predicted probabilities from random forest, a decision tree found the combined D‐dimer <1 mg/L and suPAR <11 ng/mL cutoffs, identifying 41% of patients with only 3.6% VTE probability. Conclusions Higher suPAR was associated with incident VTE independently of D‐dimer in patients hospitalized for COVID‐19. Combining suPAR and D‐dimer identified patients at low VTE risk. Registration URL: https://www.clinicaltrials.gov ; Unique identifier: NCT04818866.

Publisher

Ovid Technologies (Wolters Kluwer Health)

Subject

Cardiology and Cardiovascular Medicine

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