Copeptin: Limited Usefulness in Early Stroke Differentiation?

Background. Stroke can be a challenging diagnosis in an emergency-setting. We sought to determine whether copeptin may be a useful biomarker to differentiate between ischemic stroke (IS), transient ischemic attack (TIA), and stroke-mimics. Methods. In patients with suspected stroke arriving within 4...

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Main Authors: Johannes von Recum, Julia Searle, Anna Slagman, Jörn Ole Vollert, Matthias Endres, Martin Möckel, Martin Ebinger
Format: Article
Language:English
Published: Wiley 2015-01-01
Series:Stroke Research and Treatment
Online Access:http://dx.doi.org/10.1155/2015/768401
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author Johannes von Recum
Julia Searle
Anna Slagman
Jörn Ole Vollert
Matthias Endres
Martin Möckel
Martin Ebinger
author_facet Johannes von Recum
Julia Searle
Anna Slagman
Jörn Ole Vollert
Matthias Endres
Martin Möckel
Martin Ebinger
author_sort Johannes von Recum
collection DOAJ
description Background. Stroke can be a challenging diagnosis in an emergency-setting. We sought to determine whether copeptin may be a useful biomarker to differentiate between ischemic stroke (IS), transient ischemic attack (TIA), and stroke-mimics. Methods. In patients with suspected stroke arriving within 4.5 hours of symptom-onset, copeptin-levels were measured in initial blood-samples. The final diagnosis was adjudicated by vascular neurologists blinded to copeptin-values. Results. Of all 36 patients with available copeptin-values (median age 71 years, IQR: 54–76; 44% female), 20 patients (56%) were diagnosed with IS, no patient was diagnosed with hemorrhagic stroke, nine patients (25%) were diagnosed with TIA, and seven patients (19%) were stroke-mimics. Copeptin-levels (in pmol/L) tended to be higher in patients with IS [19.1 (11.2–48.5)] compared to TIA [9.4 (5.4–13.8)]. In stroke-mimics the range of values was extremely broad [33.3 (7.57–255.7)]. The diagnostic accuracy of copeptin for IS was 63% with a sensitivity of 80% and a positive predictive value of 64%. Conclusion. In this cohort of patients copeptin-levels within 4.5 hours of symptom onset were higher in patients with IS compared to TIA but the broad range of values in stroke-mimics limits diagnostic accuracy. This trial is registered with UTN: U1111-1119-7602.
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spelling doaj-art-699d1ceecd994b66baaf2a32c367d0952025-08-20T03:33:32ZengWileyStroke Research and Treatment2090-81052042-00562015-01-01201510.1155/2015/768401768401Copeptin: Limited Usefulness in Early Stroke Differentiation?Johannes von Recum0Julia Searle1Anna Slagman2Jörn Ole Vollert3Matthias Endres4Martin Möckel5Martin Ebinger6Division of Emergency Medicine, Department of Cardiology, Charité-Universitätsmedizin Berlin, 13353 Berlin, GermanyDivision of Emergency Medicine, Department of Cardiology, Charité-Universitätsmedizin Berlin, 13353 Berlin, GermanyDivision of Emergency Medicine, Department of Cardiology, Charité-Universitätsmedizin Berlin, 13353 Berlin, GermanyB.R.A.H.M.S GmbH, Thermo Scientific Clinical Diagnostics, 16761 Hennigsdorf, GermanyDepartment of Neurology, Charité-Universitätsmedizin Berlin, 10117 Berlin, GermanyDivision of Emergency Medicine, Department of Cardiology, Charité-Universitätsmedizin Berlin, 13353 Berlin, GermanyDepartment of Neurology, Charité-Universitätsmedizin Berlin, 10117 Berlin, GermanyBackground. Stroke can be a challenging diagnosis in an emergency-setting. We sought to determine whether copeptin may be a useful biomarker to differentiate between ischemic stroke (IS), transient ischemic attack (TIA), and stroke-mimics. Methods. In patients with suspected stroke arriving within 4.5 hours of symptom-onset, copeptin-levels were measured in initial blood-samples. The final diagnosis was adjudicated by vascular neurologists blinded to copeptin-values. Results. Of all 36 patients with available copeptin-values (median age 71 years, IQR: 54–76; 44% female), 20 patients (56%) were diagnosed with IS, no patient was diagnosed with hemorrhagic stroke, nine patients (25%) were diagnosed with TIA, and seven patients (19%) were stroke-mimics. Copeptin-levels (in pmol/L) tended to be higher in patients with IS [19.1 (11.2–48.5)] compared to TIA [9.4 (5.4–13.8)]. In stroke-mimics the range of values was extremely broad [33.3 (7.57–255.7)]. The diagnostic accuracy of copeptin for IS was 63% with a sensitivity of 80% and a positive predictive value of 64%. Conclusion. In this cohort of patients copeptin-levels within 4.5 hours of symptom onset were higher in patients with IS compared to TIA but the broad range of values in stroke-mimics limits diagnostic accuracy. This trial is registered with UTN: U1111-1119-7602.http://dx.doi.org/10.1155/2015/768401
spellingShingle Johannes von Recum
Julia Searle
Anna Slagman
Jörn Ole Vollert
Matthias Endres
Martin Möckel
Martin Ebinger
Copeptin: Limited Usefulness in Early Stroke Differentiation?
Stroke Research and Treatment
title Copeptin: Limited Usefulness in Early Stroke Differentiation?
title_full Copeptin: Limited Usefulness in Early Stroke Differentiation?
title_fullStr Copeptin: Limited Usefulness in Early Stroke Differentiation?
title_full_unstemmed Copeptin: Limited Usefulness in Early Stroke Differentiation?
title_short Copeptin: Limited Usefulness in Early Stroke Differentiation?
title_sort copeptin limited usefulness in early stroke differentiation
url http://dx.doi.org/10.1155/2015/768401
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AT juliasearle copeptinlimitedusefulnessinearlystrokedifferentiation
AT annaslagman copeptinlimitedusefulnessinearlystrokedifferentiation
AT jornolevollert copeptinlimitedusefulnessinearlystrokedifferentiation
AT matthiasendres copeptinlimitedusefulnessinearlystrokedifferentiation
AT martinmockel copeptinlimitedusefulnessinearlystrokedifferentiation
AT martinebinger copeptinlimitedusefulnessinearlystrokedifferentiation