High Plasma Levels of Activated Factor VII-Antithrombin Complex Point to Increased Tissue Factor Expression in Patients with SARS-CoV-2 Pneumonia: A Potential Link with COVID-19 Prothrombotic Diathesis
Nicola Martinelli,
Anna Maria Rigoni,
Sergio De Marchi,
Nicola Osti,
Martino Donini,
Martina Montagnana,
Annalisa Castagna,
Patrizia Pattini,
Silvia Udali,
Lucia De Franceschi,
Elisa Tinazzi,
Filippo Mazzi,
Sara Moruzzi,
Giuseppe Argentino,
Lorenzo Delfino,
Giulia Sartori,
Anna Maria Azzini,
Evelina Tacconelli,
Patrick Van Dreden,
Giuseppe Lippi,
Domenico Girelli,
Oliviero Olivieri,
Simonetta Friso,
Francesca Pizzolo
Affiliations
Nicola Martinelli
Department of Medicine, University of Verona, 37129 Verona, Italy
Anna Maria Rigoni
Angiology Unit, Department of Cardiovascular and Thoracic, Azienda Ospedaliera Universitaria Integrata, 37126 Verona, Italy
Sergio De Marchi
Department of Medicine, University of Verona, 37129 Verona, Italy
Nicola Osti
Department of Medicine, University of Verona, 37129 Verona, Italy
Martino Donini
Department of Medicine, University of Verona, 37129 Verona, Italy
Martina Montagnana
Section of Clinical Biochemistry, University of Verona, 37129 Verona, Italy
Annalisa Castagna
Department of Medicine, University of Verona, 37129 Verona, Italy
Patrizia Pattini
Department of Medicine, University of Verona, 37129 Verona, Italy
Silvia Udali
Department of Medicine, University of Verona, 37129 Verona, Italy
Lucia De Franceschi
Department of Medicine, University of Verona, 37129 Verona, Italy
Elisa Tinazzi
Department of Medicine, University of Verona, 37129 Verona, Italy
Filippo Mazzi
Department of Medicine, University of Verona, 37129 Verona, Italy
Sara Moruzzi
Department of Medicine, University of Verona, 37129 Verona, Italy
Giuseppe Argentino
Department of Medicine, University of Verona, 37129 Verona, Italy
Lorenzo Delfino
Department of Medicine, University of Verona, 37129 Verona, Italy
Giulia Sartori
Department of Medicine, University of Verona, 37129 Verona, Italy
Anna Maria Azzini
Department of Diagnostics and Public Health, University of Verona, 37129 Verona, Italy
Evelina Tacconelli
Department of Diagnostics and Public Health, University of Verona, 37129 Verona, Italy
Patrick Van Dreden
Clinical Research Department, Diagnostica Stago, 92230 Gennevilliers, France
Giuseppe Lippi
Section of Clinical Biochemistry, University of Verona, 37129 Verona, Italy
Domenico Girelli
Department of Medicine, University of Verona, 37129 Verona, Italy
Oliviero Olivieri
Department of Medicine, University of Verona, 37129 Verona, Italy
Simonetta Friso
Department of Medicine, University of Verona, 37129 Verona, Italy
Francesca Pizzolo
Department of Medicine, University of Verona, 37129 Verona, Italy
Severe acute respiratory syndrome coronavirus 2 (SARS-CoV-2) is the causal agent of coronavirus disease 2019 (COVID-19), in which coagulation abnormalities and endothelial dysfunction play a key pathogenic role. Tissue factor (TF) expression is triggered by endothelial dysfunction. Activated factor VII-antithrombin (FVIIa-AT) complex reflects indirectly FVIIa-TF interaction and has been proposed as a potential biomarker of prothrombotic diathesis. FVIIa-AT plasma concentration was measured in 40 patients (30 males and 10 females; 64.8 ± 12.3 years) admitted with SARS-CoV-2 pneumonia during the first pandemic wave in Italy. Two sex- and age-matched cohorts without COVID-19, with or without signs of systemic inflammation, were used to compare FVIIa-AT data. The FVIIa-AT plasma levels in COVID-19 patients were higher than those in non-COVID-19 subjects, either with or without inflammation, while no difference was observed among non-COVID-19 subjects. The association between COVID-19 and FVIIa-AT levels remained significant after adjustment for sex, age, C-reactive protein, renal function, fibrinogen, prothrombin time and activated partial thromboplastin time. Our results indicate that SARS-CoV-2 infection, at least during the first pandemic wave, was characterized by high FVIIa-AT levels, which may suggest an enhanced FVIIa-TF interaction in COVID-19, potentially consistent with SARS-CoV-2-induced endotheliopathy.