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Explorative investigation of biomarkers of brain damage and coagulation system activation in clinical stroke differentiation
Umeå University, Faculty of Medicine, Department of Pharmacology and Clinical Neuroscience, Neurology.ORCID iD: 0000-0001-6451-1940
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2009 (English)In: Journal of Neurology, ISSN 0340-5354, E-ISSN 1432-1459, Vol. 256, no 1, 72-77 p.Article in journal (Refereed) Published
Abstract [en]

INTRODUCTION: A simple and accurate method of differentiating ischemic stroke and intracerebral hemorrhage (ICH) is potentially useful to facilitate acute therapeutic management. Blood measurements of biomarkers of brain damage and activation of the coagulation system may potentially serve as novel diagnostic tools for stroke subtypes. METHODS: Ninety-seven stroke patients were prospectively investigated in a multicenter design with blood levels of brain biomarkers S100B, neuron specific enolase (NSE), glial fibrillary acidic protein (GFAP) as well as a coagulation biomarker, activated protein C-protein C inhibitor complex (APC-PCI), within 24 hours of symptom onset. RESULTS: Eighty-three patients (86%) had ischemic stroke and fourteen patients (14%) had ICH. There were no differences in S100B (p=0.13) and NSE (p=0.67) levels between patients with ischemic stroke or ICH. However, GFAP levels were significantly higher in ICH patients (p=0.0057). APC-PCI levels were higher in larger ischemic strokes (p=0.020). The combination of GFAP and APC-PCI levels, in patients with NIHSS score more than 3, had a sensitivity and negative predictive value of 100% for ICH in our material (p=0.0052). CONCLUSION: This exploratory study indicated that blood levels of biomarkers GFAP and APC-PCI, prior to neuroimaging, may rule out ICH in a mixed stroke population.

Place, publisher, year, edition, pages
2009. Vol. 256, no 1, 72-77 p.
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URN: urn:nbn:se:umu:diva-34695DOI: 10.1007/s00415-009-0054-8ISI: 000263978100009PubMedID: 19221847OAI: diva2:323868
Available from: 2010-06-12 Created: 2010-06-12 Last updated: 2015-10-01Bibliographically approved

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Malm, Jan
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