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Metabolic Signatures Associated with Severity in Hospitalized COVID-19 Patients

Authors :
Joan R. Masclans
Sergi Pascual-Guardia
Alex Gomez-Gomez
Judith Marin-Corral
Marcos I. Restrepo
Noemí Haro
Jose Rodríguez-Morató
R. Muñoz-Bermúdez
Oscar J. Pozo
Purificación Pérez-Terán
Olha Khymenets
Anna Salazar-Degracia
Source :
International Journal of Molecular Sciences, Vol 22, Iss 4794, p 4794 (2021), International Journal of Molecular Sciences, Volume 22, Issue 9
Publication Year :
2021
Publisher :
MDPI AG, 2021.

Abstract

The clinical evolution of COVID-19 pneumonia is poorly understood. Identifying the metabolic pathways that are altered early with viral infection and their association with disease severity is crucial to understand COVID-19 pathophysiology, and guide clinical decisions. This study aimed at assessing the critical metabolic pathways altered with disease severity in hospitalized COVID-19 patients. Forty-nine hospitalized patients with COVID-19 pneumonia were enrolled in a prospective, observational, single-center study in Barcelona, Spain. Demographic, clinical, and analytical data at admission were registered. Plasma samples were collected within the first 48 h following hospitalization. Patients were stratified based on the severity of their evolution as moderate (N = 13), severe (N = 10), or critical (N = 26). A panel of 221 biomarkers was measured by targeted metabolomics in order to evaluate metabolic changes associated with subsequent disease severity. Our results show that obesity, respiratory rate, blood pressure, and oxygen saturation, as well as some analytical parameters and radiological findings, were all associated with disease severity. Additionally, ceramide metabolism, tryptophan degradation, and reductions in several metabolic reactions involving nicotinamide adenine nucleotide (NAD) at inclusion were significantly associated with respiratory severity and correlated with inflammation. In summary, assessment of the metabolomic profile of COVID-19 patients could assist in disease severity stratification and even in guiding clinical decisions.

Details

Language :
English
ISSN :
16616596 and 14220067
Volume :
22
Issue :
4794
Database :
OpenAIRE
Journal :
International Journal of Molecular Sciences
Accession number :
edsair.doi.dedup.....c9d53d98146b60b032fa3c256f09d3e9