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Kinetics of Biomarkers of Oxidative Stress in Septic Shock: A Pilot Study
M. Helan, J. Malaska, J. Tomandl, J. Jarkovsky, K. Helanova, K. Benesova, M. Sitina, M. Dastych, T. Ondrus, M. Pavkova Goldbergova, R. Gal, P. Lokaj, M. Tomandlova, J. Parenica
Language English Country Switzerland
Document type Journal Article
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- Journal Article MeSH
Septic shock is a major cause of mortality in ICU patients, its pathophysiology is complex and not properly understood. Oxidative stress seems to be one of the most important mechanisms of shock progression to multiple organ failure. In the present pilot study, we have analysed eight oxidative-stress-related biomarkers in seven consecutive time points (i.e., the first seven days) in 21 septic shock patients admitted to the ICU. Our objective was to describe the kinetics of four biomarkers related to pro-oxidative processes (nitrite/nitrate, malondialdehyde, 8-oxo-2'-deoxyguanosine, soluble endoglin) compared to four biomarkers of antioxidant processes (the ferric reducing ability of plasma, superoxide dismutase, asymmetric dimethylarginine, mid-regional pro-adrenomedullin) and four inflammatory biomarkers (CRP, IL-6, IL-10 and neopterin). Furthermore, we analysed each biomarker's ability to predict mortality at the time of admission and 12 h after admission. Although a small number of study subjects were recruited, we have identified four promising molecules for further investigation: soluble endoglin, superoxide dismutase, asymmetric dimethylarginine and neopterin.
Department of Biochemistry Faculty of Medicine Masaryk University 625 00 Brno Czech Republic
Department of Internal Medicine and Cardiology University Hospital Brno 625 00 Brno Czech Republic
Department of Laboratory Methods Faculty of Medicine Masaryk University 625 00 Brno Czech Republic
Faculty of Medicine Masaryk University 625 00 Brno Czech Republic
International Clinical Research Center St Anne's University Hospital Brno 656 91 Brno Czech Republic
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- $a Septic shock is a major cause of mortality in ICU patients, its pathophysiology is complex and not properly understood. Oxidative stress seems to be one of the most important mechanisms of shock progression to multiple organ failure. In the present pilot study, we have analysed eight oxidative-stress-related biomarkers in seven consecutive time points (i.e., the first seven days) in 21 septic shock patients admitted to the ICU. Our objective was to describe the kinetics of four biomarkers related to pro-oxidative processes (nitrite/nitrate, malondialdehyde, 8-oxo-2'-deoxyguanosine, soluble endoglin) compared to four biomarkers of antioxidant processes (the ferric reducing ability of plasma, superoxide dismutase, asymmetric dimethylarginine, mid-regional pro-adrenomedullin) and four inflammatory biomarkers (CRP, IL-6, IL-10 and neopterin). Furthermore, we analysed each biomarker's ability to predict mortality at the time of admission and 12 h after admission. Although a small number of study subjects were recruited, we have identified four promising molecules for further investigation: soluble endoglin, superoxide dismutase, asymmetric dimethylarginine and neopterin.
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