Abstract DP256: Characteristics of Brain Structural Damage in General Population with Intracranial Artery Stenosis.

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Authors: Ziang Pan, Ziyue Liu, Xingqi Pan, Fei Han, Yi‐Cheng Zhu
Cited by: 0

Abstract

Background and aims: Covert magnetic resonance imaging (MRI) markers of cerebral small vessel disease (CSVD) can coexist with large artery atherosclerosis. We aimed to explore whether the spatial distributions of these markers were diverse in people with or without intracranial artery stenosis (ICAS). Methods: This cross-sectional analysis included 1206 stroke-free participants (aged 55.69 ± 9.27, 62.94% female) with brain MRI and MR angiography from Shunyi cohort. We analyzed the relationships between ICAS and CSVD markers. We also compared the probability maps of lacunes, cerebral microbleeds (CMB), white matter hyperintensities (WMH) and vertex-wise cortex maps at a voxel/vertex-wise level in groups with and without ICAS. Results: ICAS was significantly correlated with lacunes (OR = 2.95, 95% CI = 1.97-4.43, p < 0.001), WMH (β = 0.333, SE = 0.058, p < 0.001) and BPF (β = -0.011, SE = 0.002, p < 0.001) independently, but not with CMB. Lacunes coexist ICAS were prone in basal ganglia, while the lacunes without ICAS appeared in centrum semiovale more often. WMH with ICAS were likely to present in deep white matter involving the bilateral pyramidal tracts and superior thalamic radiation. People with ICAS were susceptible to worse cortical atrophy of right superior frontal and left rostral anterior cingulate. No obvious distributional differences were found for CMB between the two groups. Conclusions: Since ICAS may involve in the upstream pathogenesis of lacunes, white matter lesion and cortical atrophy, the impact of ICAS should not be ignored when evaluate MRI markers of CSVD.

Fields of Study & Subjects

Cerebrovascular and genetic disorders Cerebrovascular and Carotid Artery Diseases Intracerebral and Subarachnoid Hemorrhage Research

Publication details

Journal / source
Stroke
Volume
57
Issue
Suppl_1
Publication date
29 January 2026
Language
EN