Growth Differentiation Factor 15: A Prognostic Marker in Patients with Acute Chest Pain without Acute Myocardial Infarction
dc.contributor.author | Myrmel, Gard Mikael Saele | |
dc.contributor.author | Steiro, Ole-Thomas | |
dc.contributor.author | Tjora, Hilde Lunde | |
dc.contributor.author | Langørgen, Jørund | |
dc.contributor.author | Bjørneklett, Rune Oskar | |
dc.contributor.author | Skadberg, Øyvind | |
dc.contributor.author | Bonarjee, Vernon V S | |
dc.contributor.author | Mjelva, Øistein | |
dc.contributor.author | Pedersen, Eva Ringdal | |
dc.contributor.author | Vikenes, Kjell | |
dc.contributor.author | Omland, Torbjørn | |
dc.contributor.author | Aakre, Kristin Moberg | |
dc.date.accessioned | 2024-08-06T11:59:41Z | |
dc.date.available | 2024-08-06T11:59:41Z | |
dc.date.created | 2024-03-01T13:36:30Z | |
dc.date.issued | 2023 | |
dc.identifier.issn | 0009-9147 | |
dc.identifier.uri | https://hdl.handle.net/11250/3144730 | |
dc.description.abstract | Background 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.iso | eng | en_US |
dc.publisher | Oxford University Press | en_US |
dc.rights | Attribution-NonCommercial-NoDerivatives 4.0 Internasjonal | * |
dc.rights.uri | http://creativecommons.org/licenses/by-nc-nd/4.0/deed.no | * |
dc.title | Growth Differentiation Factor 15: A Prognostic Marker in Patients with Acute Chest Pain without Acute Myocardial Infarction | en_US |
dc.type | Journal article | en_US |
dc.type | Peer reviewed | en_US |
dc.description.version | publishedVersion | en_US |
dc.rights.holder | Copyright American Association for Clinical Chemistry 2023 | en_US |
cristin.ispublished | true | |
cristin.fulltext | original | |
cristin.qualitycode | 2 | |
dc.identifier.doi | 10.1093/clinchem/hvad015 | |
dc.identifier.cristin | 2251322 | |
dc.source.journal | Clinical Chemistry | en_US |
dc.source.pagenumber | 649-660 | en_US |
dc.identifier.citation | Clinical Chemistry. 2023, 69 (6), 649-660. | en_US |
dc.source.volume | 69 | en_US |
dc.source.issue | 6 | en_US |
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