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SuPAR, biomarkers of inflammation, and severe outcomes in patients hospitalized for COVID-19: The International Study of Inflammation in COVID-19.
Vasbinder, Alexi; Padalia, Kishan; Pizzo, Ian; Machado, Kristen; Catalan, Tonimarie; Presswalla, Feriel; Anderson, Elizabeth; Ismail, Anis; Hutten, Christina; Huang, Yiyuan; Blakely, Pennelope; Azam, Tariq U; Berlin, Hanna; Feroze, Rafey; Launius, Christopher; Meloche, Chelsea; Michaud, Erinleigh; O'Hayer, Patrick; Pan, Michael; Shadid, Husam R; Rasmussen, Line Jee Hartmann; Roberts, Donald A; Zhao, Lili; Banerjee, Mousumi; Murthy, Venkatesh; Loosen, Sven H; Chalkias, Athanasios; Tacke, Frank; Reiser, Jochen; Giamarellos-Bourboulis, Evangelos J; Eugen-Olsen, Jesper; Pop-Busui, Rodica; Hayek, Salim S.
Afiliação
  • Vasbinder A; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Padalia K; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Pizzo I; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Machado K; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Catalan T; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Presswalla F; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Anderson E; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Ismail A; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Hutten C; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Huang Y; Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan, USA.
  • Blakely P; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Azam TU; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Berlin H; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Feroze R; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Launius C; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Meloche C; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Michaud E; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • O'Hayer P; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Pan M; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Shadid HR; Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Rasmussen LJH; Department of Clinical Research, Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark.
  • Roberts DA; Department of Radiation Oncology, University of Michigan, Ann Arbor, Michigan, USA.
  • Zhao L; Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan, USA.
  • Banerjee M; Department of Biostatistics, School of Public Health, University of Michigan, Ann Arbor, Michigan, USA.
  • Murthy V; Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
  • Loosen SH; Clinic for Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty, University Hospital Düsseldorf, Düsseldorf, Germany.
  • Chalkias A; Institute for Translational Medicine and Therapeutics, University of Pennsylvania Perelman School of Medicine, Philadelphia, Pennsylvania, USA.
  • Tacke F; Outcomes Research Consortium, Cleveland, Ohio, USA.
  • Reiser J; Department of Hepatology and Gastroenterology, Charité-Universitätsmedizin Berlin, Berlin, Germany.
  • Giamarellos-Bourboulis EJ; Department of Medicine, Rush University Medical Center, Chicago, Illinois, USA.
  • Eugen-Olsen J; 4th Department of Internal Medicine, National and Kapodistrian University of Athens, Athens, Greece.
  • Pop-Busui R; Department of Clinical Research, Copenhagen University Hospital Amager and Hvidovre, Hvidovre, Denmark.
  • Hayek SS; Division of Endocrinology, Department of Internal Medicine, University of Michigan, Ann Arbor, Michigan, USA.
J Med Virol ; 96(1): e29389, 2024 01.
Article em En | MEDLINE | ID: mdl-38235904
ABSTRACT
Severe coronavirus disease 2019 (COVID-19) is a hyperinflammatory syndrome. The biomarkers of inflammation best suited to triage patients with COVID-19 are unknown. We conducted a prospective multicenter observational study of adult patients hospitalized specifically for COVID-19 from February 1, 2020 to October 19, 2022. Biomarkers measured included soluble urokinase plasminogen activator receptor (suPAR), C-reactive protein, interleukin-6, procalcitonin, ferritin, and D-dimer. In-hospital outcomes examined include death and the need for mechanical ventilation. Patients admitted in the United States (US, n = 1962) were used to compute area under the curves (AUCs) and identify biomarker cutoffs. The combined European cohorts (n = 1137) were used to validate the biomarker cutoffs. In the US cohort, 356 patients met the composite outcome of death (n = 197) or need for mechanical ventilation (n = 290). SuPAR was the most important predictor of the composite outcome and had the highest AUC (0.712) followed by CRP (0.642), ferritin (0.619), IL-6 (0.614), D-dimer (0.606), and lastly procalcitonin (0.596). Inclusion of other biomarkers did not improve discrimination. A suPAR cutoff of 4.0 ng/mL demonstrated a sensitivity of 95.4% (95% CI 92.4%-98.0%) and negative predictive value (NPV) of 92.5% (95% CI 87.5%-96.9%) for the composite outcome. Patients with suPAR < 4.0 ng/mL comprised 10.6% of the cohort and had a 0.8% probability of the composite outcome. Applying this cutoff to the validation cohort yielded a sensitivity of 93.8% (90.4%-96.7%) and NPV of 95.5% (93.1%-97.8%) for the composite outcome. Among commonly measured biomarkers, suPAR offered stronger discriminatory ability and may be useful in triaging low-risk patients with COVID-19.
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Ativador de Plasminogênio Tipo Uroquinase / COVID-19 Idioma: En Ano de publicação: 2024 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Receptores de Ativador de Plasminogênio Tipo Uroquinase / COVID-19 Idioma: En Ano de publicação: 2024 Tipo de documento: Article