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dc.contributor.authorHomolová, Jordanka
dc.contributor.authorJanovičová, L'ubica
dc.contributor.authorKonečná, Barbora
dc.contributor.authorVlková, Barbora
dc.contributor.authorCelec, Peter
dc.contributor.authorTóthová, L'ubomíra
dc.contributor.authorBabickova, Janka
dc.date.accessioned2021-07-07T08:33:34Z
dc.date.available2021-07-07T08:33:34Z
dc.date.created2021-01-27T16:34:28Z
dc.date.issued2020
dc.PublishedDiagnostics (Basel). 2020, 10 (3), 1-12.
dc.identifier.issn2075-4418
dc.identifier.urihttps://hdl.handle.net/11250/2763669
dc.description.abstractCurrent diagnostic methods of acute kidney injury (AKI) have limited sensitivity and specificity. Tissue injury has been linked to an increase in the concentrations of extracellular DNA (ecDNA) in plasma. A rapid turnover of ecDNA in the circulation makes it a potential marker with high sensitivity. This study aimed to analyze the concentration of ecDNA in plasma in animal models of AKI. Three different fractions of ecDNA were measured—total ecDNA was assessed fluorometrically, while nuclear ecDNA (ncDNA) and mitochondrial DNA (mtDNA) were analyzed using quantitative real-time PCR. AKI was induced using four different murine models of AKI-bilateral ureteral obstruction (BUO), glycerol-induced AKI (GLY), ischemia–reperfusion injury (IRI) and bilateral nephrectomy (BNx). Total ecDNA was significantly higher in BUO (p < 0.05) and GLY (p < 0.05) compared to the respective control groups. ncDNA was significantly higher in BUO (p < 0.05) compared to SHAM. No significant differences in the concentrations of mtDNA were found between the groups. The plasma concentrations of different fractions of ecDNA are dependent on the mechanism of induction of AKI and warrant further investigation as potential surrogate markers of AKI.en_US
dc.language.isoengen_US
dc.publisherMDPIen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titlePlasma Concentrations of Extracellular DNA in Acute Kidney Injuryen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright the authorsen_US
dc.source.articlenumber152en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.3390/diagnostics10030152
dc.identifier.cristin1880609
dc.source.journalDiagnosticsen_US
dc.source.4010
dc.source.143
dc.identifier.citationDiagnostics. 2020, 10, 152.en_US
dc.source.volume10en_US


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