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Imaging Markers of Brain Frailty and Outcome in Patients With Acute Ischemic Stroke

Bu, Ning ; Khlif, Mohamed Salah ; Lemmens, Robin ; Wouters, Anke ; Fiebach, Jochen B. ; Chamorro, Angel ; Ringelstein, E. Bernd ; Norrving, Bo LU ; Laage, Rico and Grond, Martin , et al. (2021) In Stroke 52(3). p.1004-1011
Abstract

BACKGROUND AND PURPOSE: Functional 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. METHODS: 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... (More)

BACKGROUND AND PURPOSE: Functional 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: Global brain health, as assessed by brain parenchymal fraction on magnetic resonance imaging, is associated with excellent functional outcome after ischemic stroke. Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT00927836.

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organization
publishing date
type
Contribution to journal
publication status
published
subject
keywords
atrophy, frailty, granulocyte colony, magnetic resonance imaging, stimulating factor, white matter
in
Stroke
volume
52
issue
3
pages
8 pages
publisher
American Heart Association
external identifiers
  • scopus:85102221916
  • pmid:33504185
ISSN
1524-4628
DOI
10.1161/STROKEAHA.120.029841
language
English
LU publication?
yes
id
093ced00-5b01-415a-9a8e-39fad7f72628
date added to LUP
2021-03-25 13:58:26
date last changed
2024-06-13 09:29:52
@article{093ced00-5b01-415a-9a8e-39fad7f72628,
  abstract     = {{<p>BACKGROUND AND PURPOSE: Functional 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. METHODS: 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. RESULTS: 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. CONCLUSIONS: Global brain health, as assessed by brain parenchymal fraction on magnetic resonance imaging, is associated with excellent functional outcome after ischemic stroke. Registration: URL: https://www.clinicaltrials.gov. Unique identifier: NCT00927836.</p>}},
  author       = {{Bu, Ning and Khlif, Mohamed Salah and Lemmens, Robin and Wouters, Anke and Fiebach, Jochen B. and Chamorro, Angel and Ringelstein, E. Bernd and Norrving, Bo and Laage, Rico and Grond, Martin and Wilms, Guido and Brodtmann, Amy and Thijs, Vincent}},
  issn         = {{1524-4628}},
  keywords     = {{atrophy; frailty; granulocyte colony; magnetic resonance imaging; stimulating factor; white matter}},
  language     = {{eng}},
  number       = {{3}},
  pages        = {{1004--1011}},
  publisher    = {{American Heart Association}},
  series       = {{Stroke}},
  title        = {{Imaging Markers of Brain Frailty and Outcome in Patients With Acute Ischemic Stroke}},
  url          = {{http://dx.doi.org/10.1161/STROKEAHA.120.029841}},
  doi          = {{10.1161/STROKEAHA.120.029841}},
  volume       = {{52}},
  year         = {{2021}},
}