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dc.contributor.authorKotecha, D.
dc.contributor.authorFlather, M.D.
dc.contributor.authorAtar, D.
dc.contributor.authorCollins, P.
dc.contributor.authorPepper, J.
dc.contributor.authorJenkins, E.
dc.contributor.authorReid, Christopher
dc.contributor.authorEccleston, D.
dc.date.accessioned2020-07-16T04:49:32Z
dc.date.available2020-07-16T04:49:32Z
dc.date.issued2019
dc.identifier.citationKotecha, D. and Flather, M.D. and Atar, D. and Collins, P. and Pepper, J. and Jenkins, E. and Reid, C.M. et al. 2019. B-type natriuretic peptide trumps other prognostic markers in patients assessed for coronary disease. BMC Medicine. 17 (1): Article No. 72.
dc.identifier.urihttp://hdl.handle.net/20.500.11937/80067
dc.identifier.doi10.1186/s12916-019-1306-9
dc.description.abstract

© 2019 The Author(s). Background: Risk prediction for patients with suspected coronary artery disease is complex due to the common occurrence of prior cardiovascular disease and extensive risk modification in primary care. Numerous markers have the potential to predict prognosis and guide management, but we currently lack robust 'real-world' evidence for their use. Methods: Prospective, multicentre observational study of consecutive patients referred for elective coronary angiography. Clinicians were blinded to all risk assessments, consisting of conventional factors, radial artery pulse wave analysis, 5-minute heart rate variability, high-sensitivity C-reactive protein and B-type natriuretic peptide (BNP). Blinded, independent adjudication was performed for all-cause mortality and the composite of death, myocardial infarction or stroke, analysed with Cox proportional hazards regression. Results: Five hundred twenty-two patients were assessed with median age 66 years and 21% prior revascularization. Median baseline left ventricular ejection fraction was 64%, and 62% had ≥ 50% stenosis on angiography. During 5.0 years median follow-up, 30% underwent percutaneous and 16% surgical revascularization. In multivariate analysis, only age and BNP were independently associated with outcomes. The adjusted hazard ratio per log unit increase in BNP was 2.15 for mortality (95% CI 1.45-3.19; p = 0.0001) and 1.27 for composite events (1.04-1.54; p = 0.018). Patients with baseline BNP > 100 pg/mL had substantially higher mortality and composite events (20.9% and 32.2%) than those with BNP ≤ 100 pg/mL (5.6% and 15.5%). BNP improved both classification and discrimination of outcomes (p ≤ 0.003), regardless of left ventricular systolic function. Conversely, high-sensitivity C-reactive protein, pulse wave analysis and heart rate variability were unrelated to prognosis at 5 years after risk modification and treatment of coronary disease. Conclusions: Conventional risk factors and other markers of arterial compliance, inflammation and autonomic function have limited value for prediction of outcomes in risk-modified patients assessed for coronary disease. BNP can independently identify patients with subtle impairment of cardiac function that might benefit from more intensive management. Trial registration: Clinicaltrials.gov, NCT00403351 Registered on 22 November 2006

dc.languageEnglish
dc.publisherBMC
dc.rights.urihttp://creativecommons.org/licenses/by/4.0/
dc.subjectScience & Technology
dc.subjectLife Sciences & Biomedicine
dc.subjectMedicine, General & Internal
dc.subjectGeneral & Internal Medicine
dc.subjectRisk
dc.subjectMortality
dc.subjectCoronary artery disease
dc.subjectCoronary angiography
dc.subjectB-type natriuretic peptide
dc.subjectHEART-RATE-VARIABILITY
dc.subjectCARDIOVASCULAR-DISEASE
dc.subjectMYOCARDIAL-INFARCTION
dc.subjectRISK-FACTORS
dc.subjectMORTALITY
dc.subjectEVENTS
dc.subjectDEATH
dc.subjectPREDICTION
dc.subjectPRESSURE
dc.subjectFAILURE
dc.titleB-type natriuretic peptide trumps other prognostic markers in patients assessed for coronary disease
dc.typeJournal Article
dcterms.source.volume17
dcterms.source.number1
dcterms.source.issn1741-7015
dcterms.source.titleBMC Medicine
dc.date.updated2020-07-16T04:49:28Z
curtin.note

© The Author(s). 2019 Published in BMC Medicine. This article is published under the Open Access publishing model and distributed under the terms of the Creative Commons Attribution License http://creativecommons.org/licenses/by/4.0/. Please refer to the licence to obtain terms for any further reuse or distribution of this work.

curtin.departmentSchool of Public Health
curtin.accessStatusOpen access
curtin.facultyFaculty of Health Sciences
curtin.contributor.orcidReid, Christopher [0000-0001-9173-3944]
curtin.identifier.article-numberARTN 72
dcterms.source.eissn1741-7015


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