Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/25744
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dc.contributor.authorBu, Ning-
dc.contributor.authorKhlif, Mohamed Salah-
dc.contributor.authorLemmens, Robin-
dc.contributor.authorWouters, Anke-
dc.contributor.authorFiebach, Jochen B-
dc.contributor.authorChamorro, Angel-
dc.contributor.authorRingelstein, E Bernd-
dc.contributor.authorNorrving, Bo-
dc.contributor.authorLaage, Rico-
dc.contributor.authorGrond, Martin-
dc.contributor.authorWilms, Guido-
dc.contributor.authorBrodtmann, Amy-
dc.contributor.authorThijs, Vincent N-
dc.date2021-01-28-
dc.date.accessioned2021-02-01T04:24:36Z-
dc.date.available2021-02-01T04:24:36Z-
dc.date.issued2021-03-
dc.identifier.citationStroke 2021; 52(3): 1004-1011en
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/25744-
dc.description.abstractFunctional outcome after stroke may be related to preexisting brain health. Several imaging markers of brain frailty have been described including brain atrophy and markers of small vessel disease. We investigated the association of these imaging markers with functional outcome after acute ischemic stroke. We retrospectively studied patients with acute ischemic stroke enrolled in the AXIS-2 trial (AX200 in Ischemic Stroke Trial), a randomized controlled clinical trial of granulocyte colony-stimulating factor versus placebo. We assessed the ratio of brain parenchymal volume to total intracerebral volumes (ie, the brain parenchymal fraction) and total brain volumes from routine baseline magnetic resonance imaging data obtained within 9 hours of symptom onset using the unified segmentation algorithm in SPM12. Enlarged perivascular spaces, white matter hyperintensities, lacunes, as well as a small vessel disease burden, were rated visually. Functional outcomes (modified Rankin Scale score) at day 90 were determined. Logistic regression was used to test associations between brain imaging features and functional outcomes. We enrolled 259 patients with a mean age of 69±12 years and 46 % were female. Increased brain parenchymal fraction was associated with higher odds of excellent outcome (odds ratio per percent increase, 1.078 [95% CI, 1.008-1.153]). Total brain volumes and small vessel disease burden were not associated with functional outcome. An interaction between brain parenchymal fraction and large vessel occlusion on excellent outcome was not observed. Global brain health, as assessed by brain parenchymal fraction on magnetic resonance imaging, is associated with excellent functional outcome after ischemic stroke. URL: https://www.clinicaltrials.gov. Unique identifier: NCT00927836.en
dc.language.isoeng-
dc.subjectatrophyen
dc.subjectfrailtyen
dc.subjectgranulocyte colony-stimulating factoren
dc.subjectmagnetic resonance imagingen
dc.subjectwhite matteren
dc.titleImaging Markers of Brain Frailty and Outcome in Patients With Acute Ischemic Stroke.en
dc.typeJournal Articleen
dc.identifier.journaltitleStrokeen
dc.identifier.affiliationDepartment of Neurology, the Second Affiliated Hospital of Xi'an Jiaotong University, The Florey Institute of Neuroscience and Mental Healthen
dc.identifier.affiliationDepartment of Neurology, University Hospitals Leuven, Belgiumen
dc.identifier.affiliationDementia Theme, The Florey Institute of Neuroscience and Mental Healthen
dc.identifier.affiliationDepartment of Neurosciences, Experimental Neurology, KU Leuven-University of Leuven, Belgiumen
dc.identifier.affiliationLaboratory of Neurobiology, VIB, Center for Brain & Disease Research, Leuven, Belgiumen
dc.identifier.affiliationCenter for Stroke Research, Charité, Berlin, Germanyen
dc.identifier.affiliationDepartment of Neurology, University of Barcelona, Spainen
dc.identifier.affiliationWilhelms University of Muenster, Germanyen
dc.identifier.affiliationDepartment of Clinical Sciences, Section of Neurology, Lund University, Swedenen
dc.identifier.affiliationClinical Research Department, GUIDED Development GmbH, Heidelberg, Germanyen
dc.identifier.affiliationDepartment of Neurology, Kreisklinikum Siegen, and University of Marburg Germanyen
dc.identifier.affiliationDepartment of Radiology, University Hospitals Leuven, Belgiumen
dc.identifier.affiliationDementia Theme, The Florey Institute of Neuroscience and Mental Healthen
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Healthen
dc.identifier.doi10.1161/STROKEAHA.120.029841en
dc.type.contentTexten
dc.identifier.pubmedid33504185-
local.name.researcherBrodtmann, Amy
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
item.cerifentitytypePublications-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
crisitem.author.deptNeurology-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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