Diagnostic Accuracy of Plasma Glial Fibrillary Acidic Protein for Differentiating Intracerebral Hemorrhage and Cerebral Ischemia in Patients with Symptoms of Acute Stroke

Author:

Foerch Christian1,Niessner Marion2,Back Tobias3,Bauerle Michael4,De Marchis Gian Marco5,Ferbert Andreas6,Grehl Holger7,Hamann Gerhard F8,Jacobs Andreas9,Kastrup Andreas10,Klimpe Sven11,Palm Frederick12,Thomalla Götz13,Worthmann Hans14,Sitzer Matthias115,

Affiliation:

1. Department of Neurology, Goethe-University, Frankfurt am Main, Germany

2. Roche Diagnostics, Penzberg, Germany

3. Department of Neurology, Sächsisches Krankenhaus Arnsdorf, Arnsdorf, Germany

4. Department of Neurology, Klinikum Emden, Emden, Germany

5. Department of Neurology, Inselspital, Bern, Switzerland

6. Department of Neurology, Klinikum Kassel, Kassel, Germany

7. Department of Neurology, Evangelisches und Johanniter-Klinikum, Duisburg, Germany

8. Department of Neurology, Horst Schmidt-Kliniken, Wiesbaden, Germany

9. Department of Neurology, Klinikum Fulda, Fulda, Germany

10. Department of Neurology, Klinikum Bremen-Mitte, Bremen, Germany

11. Department of Neurology, Johannes Gutenberg-Universität, Mainz, Germany

12. Department of Neurology, Städtisches Klinikum Ludwigshafen, Ludwigshafen, Germany

13. Department of Neurology, Universitätsklinikum Hamburg Eppendorf, Hamburg, Germany

14. Department of Neurology, Medizinische Hochschule Hannover, Hannover, Germany

15. Department of Neurology, Klinikum Herford, Herford, Germany

Abstract

Abstract BACKGROUND Glial fibrillary acidic protein (GFAP) is a biomarker candidate indicative of intracerebral hemorrhage (ICH) in patients with symptoms of acute stroke. GFAP is released rapidly in the presence of expanding intracerebral bleeding, whereas a more gradual release occurs in ischemic stroke. In this study the diagnostic accuracy of plasma GFAP was determined in a prospective multicenter approach. METHODS Within a 1-year recruitment period, patients suspected of having acute (symptom onset <4.5 h before admission) hemispheric stroke were prospectively included into the study in 14 stroke centers in Germany and Switzerland. A blood sample was collected at admission, and plasma GFAP was measured by use of an electrochemiluminometric immunoassay. The final diagnosis, established at hospital discharge, was classified as ICH, ischemic stroke, or stroke mimic. RESULTS The study included 205 patients (39 ICH, 163 ischemic stroke, 3 stroke mimic). GFAP concentrations were increased in patients with ICH compared with patients with ischemic stroke [median (interquartile range) 1.91 μg/L (0.41–17.66) vs 0.08 μg/L (0.02–0.14), P < 0.001]. Diagnostic accuracy of GFAP for differentiating ICH from ischemic stroke and stroke mimic was high [area under the curve 0.915 (95% CI 0.847–0.982), P < 0.001]. A GFAP cutoff of 0.29 μg/L provided diagnostic sensitivity of 84.2% and diagnostic specificity of 96.3% for differentiating ICH from ischemic stroke and stroke mimic. CONCLUSIONS Plasma GFAP analysis performed within 4.5 h of symptom onset can differentiate ICH and ischemic stroke. Studies are needed to evaluate a GFAP point-of-care system that may help optimize the prehospital triage and management of patients with symptoms of acute stroke.

Funder

Roche Diagnostics

Publisher

Oxford University Press (OUP)

Subject

Biochemistry (medical),Clinical Biochemistry

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