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dc.contributor.authorNilsen, Dennis W.T.en_US
dc.contributor.authorMjelva, Øisteinen_US
dc.contributor.authorLeon de la Fuente, Ricardoen_US
dc.contributor.authorNæsgaard, Patrycjaen_US
dc.contributor.authorPønitz, Volkeren_US
dc.contributor.authorAndersen, Trygve Bruggeren_US
dc.contributor.authorGrundt, Heidien_US
dc.contributor.authorStaines, Harryen_US
dc.contributor.authorNilsen, Stein Toreen_US
dc.date.accessioned2016-07-05T08:58:08Z
dc.date.available2016-07-05T08:58:08Z
dc.date.issued2015-04-08
dc.PublishedFrontiers in Cardiovascular Medicine 2015, 2:16eng
dc.identifier.issn2297-055X
dc.identifier.urihttps://hdl.handle.net/1956/12259
dc.description.abstractBackground: Troponin-T (TnT), high-sensitive C-reactive protein (hsCRP), and Brain Natriuretic Peptide (BNP) have been shown to be independent prognostic indicators of total and cardiac death during short- and long-term follow-up. Methods: We investigated prospectively the prognostic value of admission samples of TnT, hsCRP, and BNP in 871 chest-pain patients from South-Western Norway and 982 patients from Northern Argentina, based on a similar protocol and database setup. Follow-up was 2 years for the pooled population. The prognostic value of the selected biomarkers was investigated in quartiles of 239 patients with TnT values greater than 0.01 and up to and including 0.1 ng/mL, with continuous TnT as a potential confounder. Results: After 24 months, 69 patients had died, of whom 38 died from cardiac causes. In the selected range of TnT, this biomarker was not significantly different between patients who died and survived (mean 0.0452 and 0.0457, p = 0.887). The BNP levels were significantly higher among patients dying than in long-term survivors [340 (142–656) versus 157 (58–367) pg/mL (median, 25 and 75% percentiles), p < 0.001]. In a multivariable Cox regression model for death within 2 years, the hazard ratio (HR) for BNP in the highest quartile (Q4) as compared to the lowest (Q1) was significantly related to total mortality [HR 2.84 (95% confidence interval (CI), 1.13–7.17)], p = 0.027, in addition to age (p ≤ 0.001) and hypercholesterolemia (p = 0.043). For cardiac death, the HR for BNP was 5.18 (95% CI, 1.06–25.3), p = 0.042. Several other variables (age, congestive heart failure, ST elevation myocardial infarction, and study country) were also significantly related to cardiac death. In a multivariable Cox regression model, hsCRP rendered no significant prognostic information for all-cause mortality (p = 0.089) or for cardiac mortality (p = 0.524). Conclusion: In patients with borderline TnT values (greater than 0.01 and up to and including 0.1 ng/mL), this biomarker as well as hsCRP did not render prognostic information, whereas BNP was found to be a strong prognostic indicator of 2-year total and cardiac mortality.en_US
dc.language.isoengeng
dc.publisherFrontierseng
dc.rightsAttribution CC BYeng
dc.rights.urihttp://creativecommons.org/licenses/by/4.0eng
dc.subjectchest-paineng
dc.subjectacute coronary syndromeeng
dc.subjecttotal mortalityeng
dc.subjectcardiac mortalityeng
dc.subjectbrain natriuretic peptideeng
dc.subjecthigh sensitivity C-reactive proteineng
dc.subjectbiomarkerseng
dc.subjecttroponin-Teng
dc.titleBorderline values of troponin-T and high sensitivityC-reactive protein did not predict 2-year mortality inTnTpositive chest-pain patients, whereas brain natriureticpeptide diden_US
dc.typePeer reviewed
dc.typeJournal article
dc.date.updated2016-04-11T13:15:34Z
dc.description.versionpublishedVersionen_US
dc.rights.holderCopyright 2015 The Authors
dc.identifier.doihttps://doi.org/10.3389/fcvm.2015.00016
dc.identifier.cristin1236653
dc.subject.nsiVDP::Medisinske fag: 700::Klinisk medisinske fag: 750::Kardiologi: 771
dc.subject.nsiVDP::Midical sciences: 700::Clinical medical sciences: 750::Cardiology: 771


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