Unruptured brain arteriovenous malformations causing seizures localize to one common brain network

Seizures are a frequent symptom of unruptured brain arteriovenous malformations (bAVMs). However, the brain regions responsible for these seizures remain unclear. To identify the brain regions causally involved in bAVM‐related seizures, we retrospectively reviewed 220 patients with unruptured bAVMs....

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Veröffentlicht in:Journal of neuroscience research 2023-02, Vol.101 (2), p.245-255
Hauptverfasser: Zhao, Shao‐Zhi, Zhao, Yu‐Xin, Liao, Xiao‐Hua, Huo, Ran, Li, Hao, Jiao, Yu‐Ming, Weng, Jian‐Cong, Wang, Jie, Liu, Bing, Cao, Yong
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container_title Journal of neuroscience research
container_volume 101
creator Zhao, Shao‐Zhi
Zhao, Yu‐Xin
Liao, Xiao‐Hua
Huo, Ran
Li, Hao
Jiao, Yu‐Ming
Weng, Jian‐Cong
Wang, Jie
Liu, Bing
Cao, Yong
description Seizures are a frequent symptom of unruptured brain arteriovenous malformations (bAVMs). However, the brain regions responsible for these seizures remain unclear. To identify the brain regions causally involved in bAVM‐related seizures, we retrospectively reviewed 220 patients with unruptured bAVMs. Using voxel‐based lesion‐symptom mapping (VLSM) analyses, we tested whether individual brain regions were associated with unruptured bAVM‐related seizures. The result revealed that unruptured bAVMs causing seizures are anatomically heterogeneous at the voxel level. Subsequently, lesion network mapping (LNM) analyses was performed to determine whether bAVMs causing seizures belonged to a distributed brain network. LNM analyses indicated that these lesions were located in a functional network characterized by connectivity to the left caudate and precuneus. Moreover, the discrimination performance of the identified seizure network was evaluated in discovery set by calculating the individualized network damage score and was tested in validation set. Based on the calculated network damage scores, patients were divided into low‐, medium‐, and high‐risk groups. The prevalence of seizures significantly differed among the three risk categories in both discovery (p = .003) and validation set (p = .004). Finally, we calculated the percentage of voxels in the canonical resting‐state networks that overlapped with the seizure‐susceptible brain regions to investigate the involvement of resting‐state networks. With an involvement percentage over 50%, the frontoparietal control (82.9%), limbic function (76.7%), and default mode network (69.3%) were considered to be impacted in bAVM‐related seizures. Our study identified the seizure‐susceptible brain regions for unruptured bAVMs, which could be a plausible neuroimaging biomarker in predicting possible seizures. Seizures are a frequent symptom of unruptured brain arteriovenous malformations (bAVMs). Using VLSM and LNM analyses, we indicated that unruptured bAVMs causing seizures, while anatomically heterogeneous, were located within a common network, which could be a plausible neuroimaging biomarker for the prediction of possible seizures.
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However, the brain regions responsible for these seizures remain unclear. To identify the brain regions causally involved in bAVM‐related seizures, we retrospectively reviewed 220 patients with unruptured bAVMs. Using voxel‐based lesion‐symptom mapping (VLSM) analyses, we tested whether individual brain regions were associated with unruptured bAVM‐related seizures. The result revealed that unruptured bAVMs causing seizures are anatomically heterogeneous at the voxel level. Subsequently, lesion network mapping (LNM) analyses was performed to determine whether bAVMs causing seizures belonged to a distributed brain network. LNM analyses indicated that these lesions were located in a functional network characterized by connectivity to the left caudate and precuneus. Moreover, the discrimination performance of the identified seizure network was evaluated in discovery set by calculating the individualized network damage score and was tested in validation set. Based on the calculated network damage scores, patients were divided into low‐, medium‐, and high‐risk groups. The prevalence of seizures significantly differed among the three risk categories in both discovery (p = .003) and validation set (p = .004). Finally, we calculated the percentage of voxels in the canonical resting‐state networks that overlapped with the seizure‐susceptible brain regions to investigate the involvement of resting‐state networks. With an involvement percentage over 50%, the frontoparietal control (82.9%), limbic function (76.7%), and default mode network (69.3%) were considered to be impacted in bAVM‐related seizures. Our study identified the seizure‐susceptible brain regions for unruptured bAVMs, which could be a plausible neuroimaging biomarker in predicting possible seizures. Seizures are a frequent symptom of unruptured brain arteriovenous malformations (bAVMs). 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source MEDLINE; Wiley Online Library Journals Frontfile Complete
subjects Arteriovenous Malformations
Biomarkers
Brain
Brain - diagnostic imaging
brain arteriovenous malformations
Brain mapping
Cortex (parietal)
Damage
Humans
lesion network mapping
Lesions
Mapping
Mathematical analysis
Medical imaging
Neural networks
Neuroimaging
Retrospective Studies
Risk groups
Seizures
Seizures - diagnostic imaging
Seizures - etiology
voxel‐based lesion‐symptom mapping
title Unruptured brain arteriovenous malformations causing seizures localize to one common brain network
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