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dc.contributor.authorMyrmel, Gard Mikael Saele
dc.contributor.authorSteiro, Ole-Thomas
dc.contributor.authorTjora, Hilde Lunde
dc.contributor.authorLangørgen, Jørund
dc.contributor.authorBjørneklett, Rune Oskar
dc.contributor.authorSkadberg, Øyvind
dc.contributor.authorBonarjee, Vernon V S
dc.contributor.authorMjelva, Øistein
dc.contributor.authorPedersen, Eva Ringdal
dc.contributor.authorVikenes, Kjell
dc.contributor.authorOmland, Torbjørn
dc.contributor.authorAakre, Kristin Moberg
dc.date.accessioned2024-08-06T11:59:41Z
dc.date.available2024-08-06T11:59:41Z
dc.date.created2024-03-01T13:36:30Z
dc.date.issued2023
dc.identifier.issn0009-9147
dc.identifier.urihttps://hdl.handle.net/11250/3144730
dc.description.abstractBackground Acute chest pain is associated with an increased risk of death and cardiovascular events even when acute myocardial infarction (AMI) has been excluded. Growth differentiation factor-15 (GDF-15) is a strong prognostic marker in patients with acute chest pain and AMI, but the prognostic value in patients without AMI is uncertain. This study sought to investigate the ability of GDF-15 to predict long-term prognosis in patients presenting with acute chest pain without AMI. Methods In total, 1320 patients admitted with acute chest pain without AMI were followed for a median of 1523 days (range: 4 to 2208 days). The primary end point was all-cause mortality. Secondary end points included cardiovascular (CV) death, future AMI, heart failure hospitalization, and new-onset atrial fibrillation (AF). Results Higher concentrations of GDF-15 were associated with increased risk of death from all causes (median concentration in non-survivors vs survivors: 2124 pg/mL vs 852 pg/mL, P < 0.001), and all secondary end points. By multivariable Cox regression, GDF-15 concentration ≥4th quartile (compared to <4th quartile) remained an independent predictor of all-cause death (adjusted hazard ratio (HR): 2.75; 95% CI, 1.69–4.45, P < 0.001), CV death (adjusted HR: 3.74; 95% CI, 1.31–10.63, P = 0.013), and heart failure hospitalization (adjusted HR: 2.60; 95% CI, 1.11–6.06, P = 0.027). Adding GDF-15 to a model consisting of established risk factors and high-sensitivity cardiac troponin T (hs-cTnT) led to a significant increase in C-statistics for prediction of all-cause mortality. Conclusions Higher concentrations of GDF-15 were associated with increased risk of mortality from all causes and risk of future CV events.en_US
dc.language.isoengen_US
dc.publisherOxford University Pressen_US
dc.rightsAttribution-NonCommercial-NoDerivatives 4.0 Internasjonal*
dc.rights.urihttp://creativecommons.org/licenses/by-nc-nd/4.0/deed.no*
dc.titleGrowth Differentiation Factor 15: A Prognostic Marker in Patients with Acute Chest Pain without Acute Myocardial Infarctionen_US
dc.typeJournal articleen_US
dc.typePeer revieweden_US
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright American Association for Clinical Chemistry 2023en_US
cristin.ispublishedtrue
cristin.fulltextoriginal
cristin.qualitycode2
dc.identifier.doi10.1093/clinchem/hvad015
dc.identifier.cristin2251322
dc.source.journalClinical Chemistryen_US
dc.source.pagenumber649-660en_US
dc.identifier.citationClinical Chemistry. 2023, 69 (6), 649-660.en_US
dc.source.volume69en_US
dc.source.issue6en_US


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Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal
Except where otherwise noted, this item's license is described as Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal