Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25972
Title: Extent of FLAIR Hyperintense Vessels May Modify Treatment Effect of Thrombolysis: A Post hoc Analysis of the WAKE-UP Trial.
Austin Authors: Grosch, Anne Sophie;Kufner, Anna;Boutitie, Florent;Cheng, Bastian;Ebinger, Martin;Endres, Matthias;Fiebach, Jochen B;Fiehler, Jens;Königsberg, Alina;Lemmens, Robin;Muir, Keith W;Nighoghossian, Norbert;Pedraza, Salvador;Siemonsen, Claus Z;Thijs, Vincent ;Wouters, Anke;Gerloff, Christian;Thomalla, Götz;Galinovic, Ivana
Affiliation: Center for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germany
Excellence Cluster NeuroCure, Charite-Universitätsmedizin Berlin, Berlin, Germany
Center for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germany
Department of Neurology, Medical Park Berlin Humboldtmühle, Berlin, Germany
Hospices Civils de Lyon, Service de Biostatistique, Lyon, France
Université Lyon 1, Villeurbanne, France
Centre National de la Recherche Scientifique, Unité Mixte de Recherche 5558, Laboratoire de Biométrie et Biologie Evolutive, Equipe Biostatistique-Santé, Villeurbanne, France
Klinik und Hochschulambulanz für Neurologie, Charité-Universitätsmedizin Berlin, Berlin, Germany
Berlin Institute of Health (BIH), Berlin, Germany
Stroke Theme, Florey Institute of Neuroscience and Mental Health, University of Melbourne, Heidelberg, VIC, Australia
Neurology
Berlin Institute of Health (BIH), Berlin, Germany
German Centre for Cardiovascular Research (DZHK), Berlin, Germany
German Center for Neurodegenerative Diseases (DZNE), Berlin, Germany
Department of Neurology, University Hospitals Leuven, Leuven, Belgium
Department of Neurosciences, Experimental Neurology, Katholieke Universiteit Leuven-University of Leuven, Leuven, Belgium
Laboratory of Neurobiology, Center for Brain & Disease Research, Flanders Institute for Biotechnology, Leuven, Belgium
Department of Neurology, Head and Neurocenter, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Center for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germany
Department of Diagnostic and Interventional Neuroradiology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Department of Neurology, Head and Neurocenter, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Institute of Neuroscience & Psychology, University of Glasgow, Glasgow, United Kingdom
Department of Stroke Medicine, Claude Bernard University Lyon 1, CREATIS National Center for Scientific Research Mixed Unit of Research 5220-National Institute of Health and Medical Research U1206, National Institute of Applied Sciences of Lyon, Lyon Civil Hospices, Lyon, France
Department of Radiology, Girona Institute of Biomedical Research, Institute of Diagnostic Imaging, Dr. Josep Trueta Hospital, Girona, Spain
Department of Neurology, Aarhus University Hospital, Aarhus, Denmark
Department of Neurology, Head and Neurocenter, University Medical Center Hamburg-Eppendorf, Hamburg, Germany
Center for Stroke Research Berlin, Charité-Universitätsmedizin Berlin, Berlin, Germany
Issue Date: 4-Feb-2021
Date: 2020
Publication information: Frontiers in Neurology 2020; 11: 623881
Abstract: Background and Aims: Fluid-attenuated inversion recovery (FLAIR) hyperintense vessels (FHVs) on MRI are a radiological marker of vessel occlusion and indirect sign of collateral circulation. However, the clinical relevance is uncertain. We explored whether the extent of FHVs is associated with outcome and how FHVs modify treatment effect of thrombolysis in a subgroup of patients with confirmed unilateral vessel occlusion from the randomized controlled WAKE-UP trial. Methods: One hundred sixty-five patients were analyzed. Two blinded raters independently assessed the presence and extent of FHVs (defined as the number of slices with visible FHV multiplied by FLAIR slice thickness). Patients were then separated into two groups to distinguish between few and extensive FHVs (dichotomization at the median <30 or ≥30). Results: Here, 85% of all patients (n = 140) and 95% of middle cerebral artery (MCA) occlusion patients (n = 127) showed FHVs at baseline. Between MCA occlusion patients with few and extensive FHVs, no differences were identified in relative lesion growth (p = 0.971) and short-term [follow-up National Institutes of Health Stroke Scale (NIHSS) score; p = 0.342] or long-term functional recovery [modified Rankin Scale (mRS) <2 at 90 days poststroke; p = 0.607]. In linear regression analysis, baseline extent of FHV (defined as a continuous variable) was highly associated with volume of hypoperfused tissue (β = 2.161; 95% CI 0.96-3.36; p = 0.001). In multivariable regression analysis adjusted for treatment group, stroke severity, lesion volume, occlusion site, and recanalization, FHV did not modify functional recovery. However, in patients with few FHVs, the odds for good functional outcome (mRS) were increased in recombinant tissue plasminogen activator (rtPA) patients compared to those who received placebo [odds ratio (OR) = 5.3; 95% CI 1.2-24.0], whereas no apparent benefit was observed in patients with extensive FHVs (OR = 1.1; 95% CI 0.3-3.8), p-value for interaction was 0.11. Conclusion: While the extent of FHVs on baseline did not alter the evolution of stroke in terms of lesion progression or functional recovery, it may modify treatment effect and should therefore be considered relevant additional information in those patients who are eligible for intravenous thrombolysis. Clinical Trial Registration: Main trial (WAKE-UP): ClinicalTrials.gov, NCT01525290; and EudraCT, 2011-005906-32. Registered February 2, 2012.
URI: https://ahro.austin.org.au/austinjspui/handle/1/25972
DOI: 10.3389/fneur.2020.623881
Journal: Frontiers in Neurology
PubMed URL: 33613422
ISSN: 1664-2295
Type: Journal Article
Subjects: FLAIR hyperintensities
MRI
hyperintense vessel
ischemic Stroke
prognosis
thrombolysis
wake-up Stroke
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