Imaging Assessments and Clinical Significance of Brain Frailty in Moyamoya Disease.

AJNR Am J Neuroradiol

From the Department of Radiology (L.X.W., J.H.L., D.S.H., X.B.B., D.K.Z., H.W., L.M., X.L.), Chinese PLA General Hospital/Chinese PLA Medical School, Beijing, China

Published: July 2024

Background And Purpose: Imaging assessment of brain frailty in ischemic stroke has been extensively studied, while the correlation between brain frailty and Moyamoya disease remains obscure. This study aimed to investigate the imaging characteristics of brain frailty and its clinical applications in Moyamoya disease.

Materials And Methods: This study included 60 patients with Moyamoya disease (107 hemispheres). All patients were divided into stroke and nonstroke groups based on clinical symptoms and imaging findings. The modified brain frailty score was adapted to consider 4 imaging signs: white matter hyperintensity, enlargement of perivascular space, old vascular lesions, and cerebral microbleed. The relative CBF of the MCA territory was quantified using pseudocontinuous arterial-spin labeling. Surgical outcome after revascularization surgery was defined by the Matsushima grade.

Results: The relative CBF of the MCA territory decreased as the modified brain frailty score and periventricular white matter hyperintensity grades increased (ρ = -0.22, = .02; ρ = -0.27, = .005). Clinically, the modified brain frailty score could identify patients with Moyamoya disease with stroke (OR = 2.00, = .02). Although the modified brain frailty score showed no predictive value for surgical outcome, basal ganglia enlargement of the perivascular space had a significant correlation with the postoperative Matsushima grade (OR = 1.29, = .03).

Conclusions: The modified brain frailty score could reflect a cerebral perfusion deficit and clinical symptoms of Moyamoya disease, and its component basal ganglia enlargement of perivascular space may be a promising marker to predict surgical outcome and thus aid future clinical decision-making.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC11286025PMC
http://dx.doi.org/10.3174/ajnr.A8232DOI Listing

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