Analysis of Urinary Glycosaminoglycans to Predict Outcome in COVID-19 and Community-Acquired Pneumonia-A Proof-of-Concept Study.

1,9-dimethylmethylene blue (DMMB) COVID-19 community-acquired pneumonia endothelial dysfunction endothelial glycocalyx endotheliopathy glycosaminoglycans

Journal

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

Informations de publication

Date de publication:
13 Aug 2023
Historique:
received: 26 06 2023
revised: 02 08 2023
accepted: 10 08 2023
medline: 26 8 2023
pubmed: 26 8 2023
entrez: 26 8 2023
Statut: epublish

Résumé

Although coronavirus disease 2019 (COVID-19) is considered a systemic disease associated with vascular inflammation and eventual destruction of the protective endothelial glycocalyx (eGC), biomarkers of eGC damage are not yet available in the clinic. The most prominent components of eGC are sulphated glycosaminoglycans (sGAGs) attached to core proteoglycans. We hypothesised that the amount of sGAG fragments shed in urine (as a surrogate for systemic eGC damage) would correlate with disease severity and outcome. Total urinary sGAG concentration was measured using an in-house optimised 1,9-dimethylmethylene blue (DMMB) assay, which is highly accurate and insensitive to interferences. The median urinary sGAG concentration was significantly higher in 67 hospitalised patients with COVID-19 compared to 72 hospitalised patients with community-acquired pneumonia (CAP). In both groups, urinary sGAG concentrations predicted a combined endpoint (including intubation and death) with an area under the receiver operator characteristic curve of 0.72 (95% CI 0.55-0.88,

Identifiants

pubmed: 37629312
pii: jcm12165269
doi: 10.3390/jcm12165269
pmc: PMC10455319
pii:
doi:

Types de publication

Journal Article

Langues

eng

Subventions

Organisme : Deutsche Forschungsgemeinschaft
ID : 342 - ZA428/18-1
Organisme : Deutsche Forschungsgemeinschaft
ID : KU 2873/3-1
Organisme : Deutsche Forschungsgemeinschaft
ID : SFB 1449 / B2 to MW

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Auteurs

Alexandros Rovas (A)

Department of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Muenster, 48149 Muenster, Germany.

Julia Katharina Neumann (JK)

Department of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Muenster, 48149 Muenster, Germany.

Carolin Christina Drost (CC)

Department of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Muenster, 48149 Muenster, Germany.

Richard Vollenberg (R)

Department of Medicine B, Division of Gastroenterology, Hepatology, Endocrinology and Infectiology, University Hospital Münster, 48149 Muenster, Germany.

Gerold Thölking (G)

Department of Internal Medicine and Nephrology, Marienhospital Steinfurt, 48565 Steinfurt, Germany.

Manfred Fobker (M)

Center for Laboratory Medicine, University Hospital Münster, 48149 Muenster, Germany.

Martin Witzenrath (M)

Division of Pulmonary Inflammation, Department of Infectious Diseases and Respiratory Medicine, Charité-Universitätsmedizin Berlin, 10117 Berlin, Germany.
German Center for Lung Research (DZL), 10117 Berlin, Germany.

Philipp Kümpers (P)

Department of Medicine D, Division of General Internal and Emergency Medicine, Nephrology, and Rheumatology, University Hospital Muenster, 48149 Muenster, Germany.

Classifications MeSH