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dc.date.accessioned2018-03-19T12:15:27Z
dc.date.available2018-10-24T22:31:14Z
dc.date.created2018-01-09T14:13:32Z
dc.date.issued2017
dc.identifier.citationLyngbakken, Magnus Nakrem Pervez, Mohammad Osman Brynildsen, Jon Pedersen, Marit Holmefjord Sølvernes, Janne Christensen, Geir Arve Høiseth, Arne Didrik Omland, Torbjørn Røsjø, Helge . Fibroblast growth factor 23 in patients with acute dyspnea: Data from the Akershus Cardiac Examination (ACE) 2 Study. Clinical Biochemistry. 2017
dc.identifier.urihttp://hdl.handle.net/10852/61106
dc.description.abstractBackground Circulating fibroblast growth factor 23 (FGF23) concentrations have been linked to left ventricular remodeling and unfavorable cardiovascular outcomes, but whether FGF23 is associated with heart failure (HF) diagnosis and outcome in unselected patients with dyspnea is unknown. Accordingly, we assessed the diagnostic and prognostic properties of FGF23 in patients presenting to the emergency department with acute dyspnea. Methods and results FGF23 was measured in 314 patients admitted with acute dyspnea and the diagnostic and prognostic merit was compared to that of N-terminal pro-B-type natriuretic peptide (NT-proBNP). The diagnosis of acute HF was adjudicated by two independent physicians. Circulating FGF23 concentrations on hospital admission were higher in patients with acute HF vs. patients with non-HF related dyspnea: median 3.60 (IQR 1.24–8.77) vs. 1.00 (0.43–2.20) pmol/L; P < 0.001. The receiver-operating statistics area under the curve for acute HF diagnosis was 0.750 (0.699–0.797) for FGF23 and 0.853 (0.809–0.890) for NT-proBNP. Adjusting for clinical risk indices and cardiac biomarkers in multivariate Cox regression analysis, admission FGF23 concentrations were associated with mortality in the total study population (hazard ratio [HR] per 1 SD in lnFGF23 1.74 [1.40–2.16]). FGF23 also reclassified patients into their correct risk strata on top of clinical variables significantly associated with outcomes in the total cohort (net reclassification index 0.386 [0.161–0.612]). In patients with acute HF, both admission FGF23 and NT-proBNP concentrations were associated with mortality. Conclusion Circulating FGF23 concentrations provide incremental prognostic information to established risk indices in patients with acute dyspnea, but do not improve diagnostic accuracy over NT-proBNP measurements. Lyngbakken, Magnus Nakrem, et al. "Fibroblast growth factor 23 in patients with acute dyspnea: Data from the Akershus Cardiac Examination (ACE) 2 Study." Clinical biochemistry (2017). © 2017. This manuscript version is made available under the CC-BY-NC-ND 4.0 license.en_US
dc.languageEN
dc.language.isoenen_US
dc.publisherElsevier
dc.titleFibroblast growth factor 23 in patients with acute dyspnea: Data from the Akershus Cardiac Examination (ACE) 2 Studyen_US
dc.typeJournal articleen_US
dc.creator.authorLyngbakken, Magnus Nakrem
dc.creator.authorPervez, Mohammad Osman
dc.creator.authorBrynildsen, Jon
dc.creator.authorPedersen, Marit Holmefjord
dc.creator.authorSølvernes, Janne
dc.creator.authorChristensen, Geir Arve
dc.creator.authorHøiseth, Arne Didrik
dc.creator.authorOmland, Torbjørn
dc.creator.authorRøsjø, Helge
cristin.unitcode185,53,82,0
cristin.unitnameKlinikk for indremedisin og laboratoriefag
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.fulltextpreprint
cristin.qualitycode1
dc.identifier.cristin1538921
dc.identifier.bibliographiccitationinfo:ofi/fmt:kev:mtx:ctx&ctx_ver=Z39.88-2004&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.jtitle=Clinical Biochemistry&rft.volume=&rft.spage=&rft.date=2017
dc.identifier.jtitleClinical Biochemistry
dc.identifier.doihttp://dx.doi.org/10.1016/j.clinbiochem.2017.10.015
dc.identifier.urnURN:NBN:no-63728
dc.type.documentTidsskriftartikkelen_US
dc.type.peerreviewedPeer reviewed
dc.source.issn0009-9120
dc.identifier.fulltextFulltext https://www.duo.uio.no/bitstream/handle/10852/61106/3/ACE2_FGF23_ms_comb_rev_clean.pdf
dc.type.versionAcceptedVersion
dc.relation.projectNFR/197992


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