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dc.contributor.authorRutkovskiy, Arkady
dc.contributor.authorLyngbakken, Magnus
dc.contributor.authorDahl, Mai Britt
dc.contributor.authorBye, Anja
dc.contributor.authorPedersen, Marit Holmefjord
dc.contributor.authorWisløff, Ulrik
dc.contributor.authorChristensen, Geir Arve
dc.contributor.authorHøiseth, Arne Didrik
dc.contributor.authorOmland, Torbjørn
dc.contributor.authorRøsjø, Helge
dc.date.accessioned2022-02-28T14:52:08Z
dc.date.available2022-02-28T14:52:08Z
dc.date.created2021-06-23T09:41:35Z
dc.date.issued2021
dc.identifier.citationClinical Chemistry. 2021, 67 (6), 889-898.en_US
dc.identifier.issn0009-9147
dc.identifier.urihttps://hdl.handle.net/11250/2981826
dc.description.abstractBackground MicroRNA (miR)-210 expression is induced by acute and chronic hypoxia and provides prognostic information in patients with aortic stenosis and acute coronary syndrome. We hypothesized that circulating miR-210 concentrations could provide diagnostic and prognostic information in patients with acute heart failure (HF). Methods We measured miR-210 concentrations in serum samples on admission from 314 patients hospitalized for acute dyspnea and 9 healthy control subjects. The diagnostic and prognostic properties of miR-210 were tested in patients after adjudication of all diagnoses and with median follow-up of 464 days. Results All patients and control subjects had miR-210 concentrations within the range of detection, and the analytical variation was low as the coefficient of variation of synthetic spike-in RNA was 4%. Circulating miR-210 concentrations were increased in patients with HF compared to healthy control subjects, but miR-210 concentrations did not separate patients with acute HF (n = 143) from patients with non-HF-related dyspnea (n = 171): the area under the curve was 0.50 (95% CI 0.43–0.57). Circulating miR-210 concentrations were associated with mortality (n = 114) after adjustment for clinical risk factors (hazard ratio 1.65 [95% CI 1.03–2.62] per unit miR-210 increase), but this association was attenuated and not significant after adjustment for established cardiac protein biomarkers. Conclusions Circulating miR-210 concentrations are associated with mortality, but do not add to established protein biomarkers for diagnosis or prognosis in patients with acute dyspnea.en_US
dc.language.isoengen_US
dc.publisherOxford University Pressen_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleCirculating MicroRNA-210 Concentrations in Patients with Acute Heart Failure: Data from the Akershus Cardiac Examination 2 Studyen_US
dc.typePeer revieweden_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.source.pagenumber889-898en_US
dc.source.volume67en_US
dc.source.journalClinical Chemistryen_US
dc.source.issue6en_US
dc.identifier.doi10.1093/clinchem/hvab030
dc.identifier.cristin1917857
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2


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