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10.1016/j.redox.2020.101655

http://scihub22266oqcxt.onion/10.1016/j.redox.2020.101655
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32738789!7381406!32738789
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suck abstract from ncbi

pmid32738789      Redox+Biol 2020 ; 36 (ä): 101655
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  • Nox2 activation in Covid-19 #MMPMID32738789
  • Violi F; Oliva A; Cangemi R; Ceccarelli G; Pignatelli P; Carnevale R; Cammisotto V; Lichtner M; Alessandri F; De Angelis M; Miele MC; D'Ettorre G; Ruberto F; Venditti M; Pugliese F; Mastroianni CM
  • Redox Biol 2020[Sep]; 36 (ä): 101655 PMID32738789show ga
  • Nox2 is responsible for artery dysfunction via production of reactive oxidant species. RNA viruses may activate Nox2, but it is unknown if this occurs in coronavirus 2019(Covid-19). Nox2 activation by soluble Nox2-derived peptide(sNox2-dp) was measured in patients hospitalized for Covid-19 (n = 182) and controls (n = 91). sNox2-dp values were higher in Covid-19 patients versus controls and in severe versus non severe Covid-19. Patients with thrombotic events(n = 35,19%) had higher sNox2-dp than thrombotic event-free ones. A logistic regression analysis showed that sNox2 and coronary heart disease predicted thrombotic events. Oxidative stress by Nox2 activation is associated severe disease and thrombotic events in Covid-19 patients.
  • |Aged[MESH]
  • |Biomarkers/blood[MESH]
  • |COVID-19[MESH]
  • |Coronavirus Infections/blood/complications/*metabolism/pathology[MESH]
  • |Female[MESH]
  • |Humans[MESH]
  • |Male[MESH]
  • |Middle Aged[MESH]
  • |NADPH Oxidase 2/chemistry/*metabolism[MESH]
  • |Oxidative Stress[MESH]
  • |Pandemics[MESH]
  • |Peptide Fragments/blood[MESH]
  • |Pneumonia, Viral/blood/complications/*metabolism/pathology[MESH]


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