Utilize este identificador para referenciar este registo: http://hdl.handle.net/10451/34943
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degois.publication.firstPage1214pt_PT
degois.publication.issue12pt_PT
degois.publication.lastPage1221pt_PT
degois.publication.titleJournal of Heart and Lung Transplantationpt_PT
dc.relation.publisherversionhttps://www.sciencedirect.com/journal/the-journal-of-heart-and-lung-transplantationpt_PT
dc.contributor.authorMarques, João Silva-
dc.contributor.authorMartins, Susana Robalo-
dc.contributor.authorCalisto, Carina-
dc.contributor.authorGonçalves, Susana-
dc.contributor.authorAlmeida, Ana G.-
dc.contributor.authorSousa, João Carvalho de-
dc.contributor.authorPinto, Fausto J.-
dc.contributor.authorDiogo, António Nunes-
dc.date.accessioned2018-10-08T13:05:34Z-
dc.date.available2018-10-08T13:05:34Z-
dc.date.issued2013-
dc.identifier.citationJ Heart Lung Transplant. 2013 Dec;32(12):1214-21pt_PT
dc.identifier.issn1053-2498-
dc.identifier.urihttp://hdl.handle.net/10451/34943-
dc.descriptionCopyright © 2013 International Society for Heart and Lung Transplantation. Published by Elsevier Inc. All rights reserved.pt_PT
dc.description.abstractBACKGROUND: Pulmonary arterial hypertension (PAH) is a rare, deadly condition. Although risk stratification is extremely important for assessment of prognosis and to guide therapy, there is lack of evidence concerning the role of novel biomarkers. In a pivotal study, we sought to comparatively investigate the predictive power of several new biomarkers in PAH. METHODS: Patients with prevalent PAH were enrolled in the study protocol, which included clinical, functional and echocardiographic assessment. Blood samples were collected at baseline for determination of NT-proBNP, CT-proET-1, MR-proANP, MR-proADM, copeptin and troponin I. Patients were clinically followed-up up to 12 months for first occurrence of hospital admission due to PAH-related clinical worsening, heart/lung transplantation or all-cause mortality. RESULTS: Among the 28 included patients the pre-specified end-point occurred in 8 (29% event rate). There were higher baseline levels of CT-proET-1, copeptin, MR-proANP, NT-proBNP and troponin I in patients who reached the composite end-point. They also had larger right atria. In multivariate Cox regression, CT-proET-1 was the only biomarker associated with increased hazard of reaching the primary composite end-point (hazard ratio per tertile increase = 10.1; 95% CI 2.0 to 50.6). CONCLUSIONS: CT-proET-1 provided prognostic information independent of other biomarkers. Importantly, we have provided the first evidence that CT-proET-1 may be superior to commonly used biomarkers.pt_PT
dc.language.isoengpt_PT
dc.publisherElsevierpt_PT
dc.rightsrestrictedAccesspt_PT
dc.subjectPulmonary hypertensionpt_PT
dc.subjectPrognosispt_PT
dc.subjectBiomarkerspt_PT
dc.subjectEndothelin-1pt_PT
dc.subjectCopeptinpt_PT
dc.subjectNatriuretic peptidespt_PT
dc.subjectTroponinpt_PT
dc.titleAn exploratory panel of biomarkers for risk prediction in pulmonary hypertension : emerging role of CT-proET-1pt_PT
dc.typearticlept_PT
dc.description.versioninfo:eu-repo/semantics/publishedVersionpt_PT
dc.peerreviewedyespt_PT
degois.publication.volume32pt_PT
dc.identifier.doi10.1016/j.healun.2013.06.020pt_PT
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