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10.3390/antiox10020257

http://scihub22266oqcxt.onion/10.3390/antiox10020257
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33562403!7914603!33562403
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suck abstract from ncbi

pmid33562403      Antioxidants+(Basel) 2021 ; 10 (2): ?
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  • Oxidative Stress Status in COVID-19 Patients Hospitalized in Intensive Care Unit for Severe Pneumonia A Pilot Study #MMPMID33562403
  • Pincemail J; Cavalier E; Charlier C; Cheramy-Bien JP; Brevers E; Courtois A; Fadeur M; Meziane S; Goff CL; Misset B; Albert A; Defraigne JO; Rousseau AF
  • Antioxidants (Basel) 2021[Feb]; 10 (2): ? PMID33562403show ga
  • BACKGROUND: A key role of oxidative stress has been highlighted in the pathogenesis of COVID-19. However, little has been said about oxidative stress status (OSS) of COVID-19 patients hospitalized in intensive care unit (ICU). MATERIAL AND METHODS: Biomarkers of the systemic OSS included antioxidants (9 assays), trace elements (3 assays), inflammation markers (4 assays) and oxidative damage to lipids (3 assays). RESULTS: Blood samples were drawn after 9 (7-11) and 41 (39-43) days of ICU stay, respectively in 3 and 6 patients. Vitamin C, thiol proteins, reduced glutathione, gamma-tocopherol, beta-carotene and PAOT((R)) score were significantly decreased compared to laboratory reference values. Selenium concentration was at the limit of the lower reference value. By contrast, the copper/zinc ratio (as a source of oxidative stress) was higher than reference values in 55% of patients while copper was significantly correlated with lipid peroxides (r = 0.95, p < 0.001). Inflammatory biomarkers (C-reactive protein and myeloperoxidase) were significantly increased when compared to normals. CONCLUSIONS: The systemic OSS was strongly altered in critically ill COVID-19 patients as evidenced by increased lipid peroxidation but also by deficits in some antioxidants (vitamin C, glutathione, thiol proteins) and trace elements (selenium).
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