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Integrated NMR and MS Analysis of the Plasma Metabolome Reveals Major Changes in One-Carbon, Lipid, and Amino Acid Metabolism in Severe and Fatal Cases of COVID-19

Authors :
Marcos C. Gama-Almeida
Gabriela D. A. Pinto
Lívia Teixeira
Eugenio D. Hottz
Paula Ivens
Hygor Ribeiro
Rafael Garrett
Alexandre G. Torres
Talita I. A. Carneiro
Bianca de O. Barbalho
Christian Ludwig
Claudio J. Struchiner
Iranaia Assunção-Miranda
Ana Paula C. Valente
Fernando A. Bozza
Patrícia T. Bozza
Gilson C. dos Santos
Tatiana El-Bacha
Source :
Metabolites, Vol 13, Iss 7, p 879 (2023)
Publication Year :
2023
Publisher :
MDPI AG, 2023.

Abstract

Brazil has the second-highest COVID-19 death rate worldwide, and Rio de Janeiro is among the states with the highest rate in the country. Although vaccine coverage has been achieved, it is anticipated that COVID-19 will transition into an endemic disease. It is concerning that the molecular mechanisms underlying clinical evolution from mild to severe disease, as well as the mechanisms leading to long COVID-19, are not yet fully understood. NMR and MS-based metabolomics were used to identify metabolites associated with COVID-19 pathophysiology and disease outcome. Severe COVID-19 cases (n = 35) were enrolled in two reference centers in Rio de Janeiro within 72 h of ICU admission, alongside 12 non-infected control subjects. COVID-19 patients were grouped into survivors (n = 18) and non-survivors (n = 17). Choline-related metabolites, serine, glycine, and betaine, were reduced in severe COVID-19, indicating dysregulation in methyl donors. Non-survivors had higher levels of creatine/creatinine, 4-hydroxyproline, gluconic acid, and N-acetylserine, indicating liver and kidney dysfunction. Several changes were greater in women; thus, patients’ sex should be considered in pandemic surveillance to achieve better disease stratification and improve outcomes. These metabolic alterations may be useful to monitor organ (dys) function and to understand the pathophysiology of acute and possibly post-acute COVID-19 syndromes.

Details

Language :
English
ISSN :
22181989
Volume :
13
Issue :
7
Database :
Directory of Open Access Journals
Journal :
Metabolites
Publication Type :
Academic Journal
Accession number :
edsdoj.864e801ccb463f89651876d0b39350
Document Type :
article
Full Text :
https://doi.org/10.3390/metabo13070879