Blood-brain barrier leakage increases with small vessel disease in acute ischemic stroke

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Blood-brain barrier leakage increases with small vessel disease in acute ischemic stroke. / Arba, Francesco; Leigh, Richard; Inzitari, Domenico; Warach, Steven J; Luby, Marie; Lees, Kennedy R; STIR/VISTA Imaging Collaboration.

In: NEUROLOGY, Vol. 89, No. 21, 21.11.2017, p. 2143-2150.

Research output: SCORING: Contribution to journalSCORING: Journal articleResearchpeer-review

Harvard

Arba, F, Leigh, R, Inzitari, D, Warach, SJ, Luby, M, Lees, KR & STIR/VISTA Imaging Collaboration 2017, 'Blood-brain barrier leakage increases with small vessel disease in acute ischemic stroke', NEUROLOGY, vol. 89, no. 21, pp. 2143-2150. https://doi.org/10.1212/WNL.0000000000004677

APA

Arba, F., Leigh, R., Inzitari, D., Warach, S. J., Luby, M., Lees, K. R., & STIR/VISTA Imaging Collaboration (2017). Blood-brain barrier leakage increases with small vessel disease in acute ischemic stroke. NEUROLOGY, 89(21), 2143-2150. https://doi.org/10.1212/WNL.0000000000004677

Vancouver

Arba F, Leigh R, Inzitari D, Warach SJ, Luby M, Lees KR et al. Blood-brain barrier leakage increases with small vessel disease in acute ischemic stroke. NEUROLOGY. 2017 Nov 21;89(21):2143-2150. https://doi.org/10.1212/WNL.0000000000004677

Bibtex

@article{86c209b5c60648aab37fe149170d5696,
title = "Blood-brain barrier leakage increases with small vessel disease in acute ischemic stroke",
abstract = "OBJECTIVE: In patients with acute ischemic stroke, we aimed to investigate the relation between preexisting small vessel disease (SVD) and the amount of blood-brain barrier (BBB) leakage in ischemic and nonischemic area before IV thrombolysis.METHODS: We retrospectively accessed anonymous patient-level data from the Stroke Imaging Repository and the Virtual International Stroke Trials Archive resources and included patients treated with IV thrombolysis with pretreatment MRI. We rated SVD features using validated qualitative magnetic resonance (MR) scales. Leakage of BBB was assessed with postprocessing of perfusion-weighted images. We evaluated associations between SVD features (individually and summed in a global SVD score) and BBB leakage using linear regression analysis, adjusting for major clinical confounders.RESULTS: A total of 212 patients, mean age (±SD) 69.5 years (±16.1), 102 (48%) male, had available MR before IV thrombolysis. Evidence of BBB leakage was present in 175 (80%) and 205 (94%) patients in the ischemic and nonischemic area, respectively. Lacunar infarcts (β = 0.17, p = 0.042) were associated with BBB leakage in the ischemic area, and brain atrophy was associated with BBB leakage in both ischemic (β = 0.20, p = 0.026) and nonischemic (β = 0.27, p = 0.001) areas. Increasing SVD grade was independently associated with BBB leakage in both ischemic (β = 0.26, p = 0.007) and nonischemic (β = 0.27, p = 0.003) area.CONCLUSIONS: Global SVD burden is associated with increased BBB leakage in both acutely ischemic and nonischemic area. Our results support that SVD score has construct validity, and confirm a relation between SVD and BBB disruption also in patients with acute stroke.",
keywords = "Aged, Aged, 80 and over, Analysis of Variance, Blood-Brain Barrier, Brain Ischemia, Cerebral Small Vessel Diseases, Female, Humans, Magnetic Resonance Imaging, Male, Middle Aged, Multivariate Analysis, Stroke, Tomography, X-Ray Computed, Journal Article",
author = "Francesco Arba and Richard Leigh and Domenico Inzitari and Warach, {Steven J} and Marie Luby and Lees, {Kennedy R} and {STIR/VISTA Imaging Collaboration}",
note = "{\textcopyright} 2017 American Academy of Neurology.",
year = "2017",
month = nov,
day = "21",
doi = "10.1212/WNL.0000000000004677",
language = "English",
volume = "89",
pages = "2143--2150",
journal = "NEUROLOGY",
issn = "0028-3878",
publisher = "Lippincott Williams and Wilkins",
number = "21",

}

RIS

TY - JOUR

T1 - Blood-brain barrier leakage increases with small vessel disease in acute ischemic stroke

AU - Arba, Francesco

AU - Leigh, Richard

AU - Inzitari, Domenico

AU - Warach, Steven J

AU - Luby, Marie

AU - Lees, Kennedy R

AU - STIR/VISTA Imaging Collaboration

N1 - © 2017 American Academy of Neurology.

PY - 2017/11/21

Y1 - 2017/11/21

N2 - OBJECTIVE: In patients with acute ischemic stroke, we aimed to investigate the relation between preexisting small vessel disease (SVD) and the amount of blood-brain barrier (BBB) leakage in ischemic and nonischemic area before IV thrombolysis.METHODS: We retrospectively accessed anonymous patient-level data from the Stroke Imaging Repository and the Virtual International Stroke Trials Archive resources and included patients treated with IV thrombolysis with pretreatment MRI. We rated SVD features using validated qualitative magnetic resonance (MR) scales. Leakage of BBB was assessed with postprocessing of perfusion-weighted images. We evaluated associations between SVD features (individually and summed in a global SVD score) and BBB leakage using linear regression analysis, adjusting for major clinical confounders.RESULTS: A total of 212 patients, mean age (±SD) 69.5 years (±16.1), 102 (48%) male, had available MR before IV thrombolysis. Evidence of BBB leakage was present in 175 (80%) and 205 (94%) patients in the ischemic and nonischemic area, respectively. Lacunar infarcts (β = 0.17, p = 0.042) were associated with BBB leakage in the ischemic area, and brain atrophy was associated with BBB leakage in both ischemic (β = 0.20, p = 0.026) and nonischemic (β = 0.27, p = 0.001) areas. Increasing SVD grade was independently associated with BBB leakage in both ischemic (β = 0.26, p = 0.007) and nonischemic (β = 0.27, p = 0.003) area.CONCLUSIONS: Global SVD burden is associated with increased BBB leakage in both acutely ischemic and nonischemic area. Our results support that SVD score has construct validity, and confirm a relation between SVD and BBB disruption also in patients with acute stroke.

AB - OBJECTIVE: In patients with acute ischemic stroke, we aimed to investigate the relation between preexisting small vessel disease (SVD) and the amount of blood-brain barrier (BBB) leakage in ischemic and nonischemic area before IV thrombolysis.METHODS: We retrospectively accessed anonymous patient-level data from the Stroke Imaging Repository and the Virtual International Stroke Trials Archive resources and included patients treated with IV thrombolysis with pretreatment MRI. We rated SVD features using validated qualitative magnetic resonance (MR) scales. Leakage of BBB was assessed with postprocessing of perfusion-weighted images. We evaluated associations between SVD features (individually and summed in a global SVD score) and BBB leakage using linear regression analysis, adjusting for major clinical confounders.RESULTS: A total of 212 patients, mean age (±SD) 69.5 years (±16.1), 102 (48%) male, had available MR before IV thrombolysis. Evidence of BBB leakage was present in 175 (80%) and 205 (94%) patients in the ischemic and nonischemic area, respectively. Lacunar infarcts (β = 0.17, p = 0.042) were associated with BBB leakage in the ischemic area, and brain atrophy was associated with BBB leakage in both ischemic (β = 0.20, p = 0.026) and nonischemic (β = 0.27, p = 0.001) areas. Increasing SVD grade was independently associated with BBB leakage in both ischemic (β = 0.26, p = 0.007) and nonischemic (β = 0.27, p = 0.003) area.CONCLUSIONS: Global SVD burden is associated with increased BBB leakage in both acutely ischemic and nonischemic area. Our results support that SVD score has construct validity, and confirm a relation between SVD and BBB disruption also in patients with acute stroke.

KW - Aged

KW - Aged, 80 and over

KW - Analysis of Variance

KW - Blood-Brain Barrier

KW - Brain Ischemia

KW - Cerebral Small Vessel Diseases

KW - Female

KW - Humans

KW - Magnetic Resonance Imaging

KW - Male

KW - Middle Aged

KW - Multivariate Analysis

KW - Stroke

KW - Tomography, X-Ray Computed

KW - Journal Article

U2 - 10.1212/WNL.0000000000004677

DO - 10.1212/WNL.0000000000004677

M3 - SCORING: Journal article

C2 - 29070665

VL - 89

SP - 2143

EP - 2150

JO - NEUROLOGY

JF - NEUROLOGY

SN - 0028-3878

IS - 21

ER -