Circulating Osteopontin Levels and Outcomes in Patients Hospitalized for COVID-19.

CRP OPN PCT SARS-CoV-2 coronavirus disease 2019 death mechanical ventilation outcomes procalcitonin renal replacement therapy risk prediction

Journal

Journal of clinical medicine
ISSN: 2077-0383
Titre abrégé: J Clin Med
Pays: Switzerland
ID NLM: 101606588

Informations de publication

Date de publication:
30 Aug 2021
Historique:
received: 07 07 2021
revised: 16 08 2021
accepted: 26 08 2021
entrez: 10 9 2021
pubmed: 11 9 2021
medline: 11 9 2021
Statut: epublish

Résumé

Severe coronavirus disease 2019 (COVID-19) is the result of a hyper-inflammatory reaction to the severe acute respiratory syndrome coronavirus 2. The biomarkers of inflammation have been used to risk-stratify patients with COVID-19. Osteopontin (OPN) is an integrin-binding glyco-phosphoprotein involved in the modulation of leukocyte activation; its levels are associated with worse outcomes in patients with sepsis. Whether OPN levels predict outcomes in COVID-19 is unknown. We measured OPN levels in serum of 341 hospitalized COVID-19 patients collected within 48 h from admission. We characterized the determinants of OPN levels and examined their association with in-hospital outcomes; notably death, need for mechanical ventilation, and need for renal replacement therapy (RRT) and as a composite outcome. The risk discrimination ability of OPN was compared with other inflammatory biomarkers. Patients with COVID-19 (mean age 60, 61.9% male, 27.0% blacks) had significantly higher levels of serum OPN compared to healthy volunteers (96.63 vs. 16.56 ng/mL, Higher OPN levels are associated with increased odds of death and mechanical ventilation in patients with COVID-19, however, their utility in triage is questionable.

Sections du résumé

BACKGROUND BACKGROUND
Severe coronavirus disease 2019 (COVID-19) is the result of a hyper-inflammatory reaction to the severe acute respiratory syndrome coronavirus 2. The biomarkers of inflammation have been used to risk-stratify patients with COVID-19. Osteopontin (OPN) is an integrin-binding glyco-phosphoprotein involved in the modulation of leukocyte activation; its levels are associated with worse outcomes in patients with sepsis. Whether OPN levels predict outcomes in COVID-19 is unknown.
METHODS METHODS
We measured OPN levels in serum of 341 hospitalized COVID-19 patients collected within 48 h from admission. We characterized the determinants of OPN levels and examined their association with in-hospital outcomes; notably death, need for mechanical ventilation, and need for renal replacement therapy (RRT) and as a composite outcome. The risk discrimination ability of OPN was compared with other inflammatory biomarkers.
RESULTS RESULTS
Patients with COVID-19 (mean age 60, 61.9% male, 27.0% blacks) had significantly higher levels of serum OPN compared to healthy volunteers (96.63 vs. 16.56 ng/mL,
CONCLUSION CONCLUSIONS
Higher OPN levels are associated with increased odds of death and mechanical ventilation in patients with COVID-19, however, their utility in triage is questionable.

Identifiants

pubmed: 34501358
pii: jcm10173907
doi: 10.3390/jcm10173907
pmc: PMC8432103
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : NIDDK NIH HHS
ID : U01 DK119083
Pays : United States
Organisme : NHLBI NIH HHS
ID : R01 HL153384
Pays : United States
Organisme : Wellcome Trust
ID : 110043
Pays : United Kingdom
Organisme : NIDDK NIH HHS
ID : U2C DK110768
Pays : United States
Organisme : NHLBI NIH HHS
ID : 1R01HL153384-01
Pays : United States
Organisme : NIDDK NIH HHS
ID : R01 DK128012
Pays : United States

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Auteurs

Salim S Hayek (SS)

Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.

Christoph Roderburg (C)

Clinic for Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty, University Hospital Düsseldorf, 40225 Düsseldorf, Germany.

Pennelope Blakely (P)

Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.

Christopher Launius (C)

Division of Cardiology, Department of Internal Medicine, University of Michigan, Ann Arbor, MI 48109, USA.

Jesper Eugen-Olsen (J)

Department of Clinical Research, Copenhagen University Hospital Amager and Hvidovre, 2650 Hvidovre, Denmark.

Frank Tacke (F)

Department of Hepatology and Gastroenterology, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.

Sofia Ktena (S)

4th Department of Internal Medicine, National and Kapodistrian University of Athens, Medial School, 12462 Athens, Greece.

Verena Keitel (V)

Clinic for Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty, University Hospital Düsseldorf, 40225 Düsseldorf, Germany.

Mark Luedde (M)

KGP Bremerhaven, Postbrookstraße 103, 27574 Bremerhaven, Germany.

Evangelos J Giamarellos-Bourboulis (EJ)

4th Department of Internal Medicine, National and Kapodistrian University of Athens, Medial School, 12462 Athens, Greece.

Tom Luedde (T)

Clinic for Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty, University Hospital Düsseldorf, 40225 Düsseldorf, Germany.

Sven H Loosen (SH)

Clinic for Gastroenterology, Hepatology and Infectious Diseases, Medical Faculty, University Hospital Düsseldorf, 40225 Düsseldorf, Germany.

Classifications MeSH