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dc.contributor.authorAakre, Kristin Moberg
dc.contributor.authorOttesen, Anett Hellebø
dc.contributor.authorStrand, Heidi
dc.contributor.authorFaaren, Arne L.
dc.contributor.authorAlaour, Bashir
dc.contributor.authorTorsvik, Janniche
dc.contributor.authorSylte, Marit Sverresdotter
dc.contributor.authorMarber, Michael
dc.contributor.authorChristensen, Geir
dc.contributor.authorRøsjø, Helge Rørvik
dc.contributor.authorOmland, Torbjørn
dc.date.accessioned2022-03-25T12:22:02Z
dc.date.available2022-03-25T12:22:02Z
dc.date.created2021-11-12T13:22:10Z
dc.date.issued2021
dc.identifier.issn0009-9120
dc.identifier.urihttps://hdl.handle.net/11250/2987644
dc.description.abstractBackground Secretoneurin is a novel prognostic biomarker that may predict mortality in heart failure and the occurrence of ventricular arrhythmias. This study reports the within subject variation (CVI), between subject variation (CVG), reference change values (RCV) and index of individuality (II) of secretoneurin. Methods Thirty healthy volunteers were included. Non-fasting samples were obtained between 8 and 10 am once a week for ten weeks. Secretoneurin was analyzed in duplicate using ELISA. No outliers were present according to Burnett and Reeds‘ criteria. Simple linear regression did not identify significant trends. Variance homogeneity in the analytical variance and CVI were tested using Cochrane’s and Bartlett’s tests and four participants were excluded. Calculation of CVI, CVG and RCV were done on ln transformed data as described by Fokkema, the II was calculated using retransformed data. Results The median age of the participants was 36 years and 53% were female. Non-fasting glucose, eGFR(CKD-EPI), cTnT and NT-proBNP concentrations were within the normal range. Median secretoneurin concentrations were 38 pmol/L (women) and 33 pmol/L (men), p-value < 0.001. CVI and CVG were 9.8% (CI 8.7% to 11.0%) and 20.0 (CI 15.4% to 28.0%), respectively. RCV were 38.7% (CI 35.5% to 42.7%) and −27.9 (CI −29.9 to −26.2) and the II were 0.60 (CI 0.42–0.78). No gender differences were present. Conclusion Secretoneurin has a fairly low CVI, CVG, RCV and II, indicating that it could be suitable as a diagnostic or prognostic biomarker and that delta values in serial samplings may be preferable for identifying clinical changes.en_US
dc.language.isoengen_US
dc.publisherElsevieren_US
dc.rightsNavngivelse 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/deed.no*
dc.titleBiological variation of secretoneurin; a novel cardiovascular biomarker implicated in arrhythmogenesisen_US
dc.typeJournal articleen_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2021 The Author(s)en_US
cristin.ispublishedtrue
cristin.fulltextpreprint
cristin.fulltextoriginal
cristin.qualitycode1
dc.identifier.doi10.1016/j.clinbiochem.2021.09.014
dc.identifier.cristin1954108
dc.source.journalClinical Biochemistryen_US
dc.source.pagenumber74-77en_US
dc.identifier.citationClinical Biochemistry. 2021, 98, 74-77.en_US
dc.source.volume98en_US


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