Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/28868
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dc.contributor.authorBu, Ning-
dc.contributor.authorChurilov, Leonid-
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-
dc.date.accessioned2022-02-22T04:30:50Z-
dc.date.available2022-02-22T04:30:50Z-
dc.date.issued2022-01-28-
dc.identifier.citationFrontiers in neurology 2021; 12: 747343en
dc.identifier.issn1664-2295
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/28868-
dc.description.abstractThe evolution of total brain volume early after stroke is not well understood. We investigated the associations between age and imaging features and brain volume change in the first month after stroke. We retrospectively studied patients with acute ischemic stroke enrolled in the AXIS-2 trial. Total brain volume change from hyperacute MRI data to the first month after stroke was assessed using unified segmentation in SPM12. We hypothesized that age, ischemic brain lesion size, and white matter (WM) changes were associated with larger brain volume change. Enlarged perivascular spaces (EPVSs) and white matter hyperintensities (WMHs) were rated visually and the presence of lacunes was assessed. We enrolled 173 patients with a mean age of 67 ± 11 years, 44% were women. There was a median 6 ml decrease in volume (25th percentile -1 ml to 75th percentile 21 ml) over time, equivalent to a median 0.5% (interquartile range [IQR], -0.07%-1.4%), decrease in brain volume. Age was associated with larger brain volume loss (per 10 years of age, 5 ml 95% CI 2-8 ml). Baseline diffusion weighted imaging (DWI) lesion volume was not associated with greater volume loss per 10 ml of lesion volume, change by 0 ml (95% CI -0.1 to 0.1 ml). Increasing Fazekas scores of deep WMH were associated with greater tissue loss (5 ml, 95% CI 1-10 ml). Total brain volume changes in a heterogenous fashion after stroke. Volume loss occurs over 1 month after stroke and is associated with age and deep WM disease. We did not find evidence that more severe strokes lead to increased early tissue loss.en
dc.language.isoeng
dc.subjectatrophyen
dc.subjectbrain volume changesen
dc.subjectclinical trialen
dc.subjectedemaen
dc.subjecthemorrhagic transformationen
dc.subjectischemic strokeen
dc.titleEarly Brain Volume Changes After Stroke: Subgroup Analysis From the AXIS-2 Trial.en
dc.typeJournal Articleen
dc.identifier.journaltitleFrontiers in neurologyen
dc.identifier.affiliationThe Florey Institute of Neuroscience and Mental Health..en
dc.identifier.affiliationDepartment of Medicine and Neurology, Melbourne Brain Centre, University of Melbourne, Melbourne, VIC, Australia..en
dc.identifier.affiliationDepartment of Medicine, University of Melbourne, Melbourne, VIC, Australia..en
dc.identifier.affiliationDepartment of Neurology, University of Barcelona, Barcelona, Spain..en
dc.identifier.affiliationDepartment of Neurosciences, Experimental Neurology, KU Leuven - University of Leuven, Leuven, Belgium..en
dc.identifier.affiliationLaboratory of Neurobiology, VIB, Center for Brain & Disease Research, Leuven, Belgium..en
dc.identifier.affiliationDepartment of Neurology, University Hospitals Leuven, Leuven, Belgium..en
dc.identifier.affiliationCenter for Stroke Research, Charité University Medicine Berlin, Berlin, Germany..en
dc.identifier.affiliationDepartment of Neurology, Wilhelms University of Muenster, Münster, Germany..en
dc.identifier.affiliationSection of Neurology, Department of Clinical Sciences, Lund University, Lund, Sweden..en
dc.identifier.affiliationDepartment of Clinical Research, Guided Development GmbH, Heidelberg, Germany..en
dc.identifier.affiliationDepartment of Neurology, Kreisklinikum Siegen, University of Marburg Germany, Marburg, Germany..en
dc.identifier.affiliationDepartment of Radiology, University Hospitals of Leuven, Leuven, Belgium..en
dc.identifier.affiliationDepartment of Neurology, The Second Affiliated Hospital of Xi'an Jiaotong University, Xi'an, China..en
dc.identifier.pubmedurihttps://pubmed.ncbi.nlm.nih.gov/35153972/en
dc.identifier.doi10.3389/fneur.2021.747343en
dc.type.contentTexten
dc.identifier.orcid0000-0001-7329-2786en
dc.identifier.orcid0000-0002-6614-8417en
dc.identifier.orcid0000-0002-9807-6606en
dc.identifier.orcid0000-0002-0096-434Xen
dc.identifier.orcid0000-0001-9466-2862en
dc.identifier.pubmedid35153972
local.name.researcherBrodtmann, Amy
item.fulltextNo Fulltext-
item.grantfulltextnone-
item.cerifentitytypePublications-
item.openairetypeJournal Article-
item.languageiso639-1en-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptMedicine (University of Melbourne)-
crisitem.author.deptThe Florey Institute of Neuroscience and Mental Health-
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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