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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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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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.</description><identifier>ISSN: 0360-4012</identifier><identifier>EISSN: 1097-4547</identifier><identifier>DOI: 10.1002/jnr.25142</identifier><identifier>PMID: 36345215</identifier><language>eng</language><publisher>United States: Wiley Subscription Services, Inc</publisher><subject>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</subject><ispartof>Journal of neuroscience research, 2023-02, Vol.101 (2), p.245-255</ispartof><rights>2022 The Authors. published by Wiley Periodicals LLC.</rights><rights>2022 The Authors. Journal of Neuroscience Research published by Wiley Periodicals LLC.</rights><rights>2022. This article is published under http://creativecommons.org/licenses/by-nc-nd/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3742-e8e0dd3a702867b233bba10476f255746349ac528f7de6c00d2f73a0c6521ec43</citedby><cites>FETCH-LOGICAL-c3742-e8e0dd3a702867b233bba10476f255746349ac528f7de6c00d2f73a0c6521ec43</cites><orcidid>0000-0003-2029-5187 ; 0000-0002-8289-1120</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1002%2Fjnr.25142$$EPDF$$P50$$Gwiley$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1002%2Fjnr.25142$$EHTML$$P50$$Gwiley$$Hfree_for_read</linktohtml><link.rule.ids>230,314,776,780,881,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36345215$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Zhao, Shao‐Zhi</creatorcontrib><creatorcontrib>Zhao, Yu‐Xin</creatorcontrib><creatorcontrib>Liao, Xiao‐Hua</creatorcontrib><creatorcontrib>Huo, Ran</creatorcontrib><creatorcontrib>Li, Hao</creatorcontrib><creatorcontrib>Jiao, Yu‐Ming</creatorcontrib><creatorcontrib>Weng, Jian‐Cong</creatorcontrib><creatorcontrib>Wang, Jie</creatorcontrib><creatorcontrib>Liu, Bing</creatorcontrib><creatorcontrib>Cao, Yong</creatorcontrib><title>Unruptured brain arteriovenous malformations causing seizures localize to one common brain network</title><title>Journal of neuroscience research</title><addtitle>J Neurosci Res</addtitle><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.</description><subject>Arteriovenous Malformations</subject><subject>Biomarkers</subject><subject>Brain</subject><subject>Brain - diagnostic imaging</subject><subject>brain arteriovenous malformations</subject><subject>Brain mapping</subject><subject>Cortex (parietal)</subject><subject>Damage</subject><subject>Humans</subject><subject>lesion network mapping</subject><subject>Lesions</subject><subject>Mapping</subject><subject>Mathematical analysis</subject><subject>Medical imaging</subject><subject>Neural networks</subject><subject>Neuroimaging</subject><subject>Retrospective Studies</subject><subject>Risk groups</subject><subject>Seizures</subject><subject>Seizures - diagnostic imaging</subject><subject>Seizures - etiology</subject><subject>voxel‐based lesion‐symptom mapping</subject><issn>0360-4012</issn><issn>1097-4547</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>24P</sourceid><sourceid>WIN</sourceid><sourceid>EIF</sourceid><recordid>eNp1kc1u1DAUhS0EosPAoi-ALLEpi7TXf3Fmhaqq_KlqJUTXluPctJ4m9tROWrVPj2GGCpBYeeHPn8-9h5B9BocMgB-tQzrkikn-jCwYrHQlldTPyQJEDZUExvfIq5zXALBaKfGS7IlaSMWZWpD2MqR5M80JO9om6wO1acLk4x2GOGc62qGPabSTjyFTZ-fswxXN6B_Lk0yH6OzgH5FOkcaA1MVxjGFnCjjdx3Tzmrzo7ZDxze5cksuPp99PPldnF5--nByfVU5oyStsELpOWA28qXXLhWhby0DquudKaVkir6xTvOl1h7UD6HivhQVXl0nQSbEkH7bezdyO2DkMU7KD2SQ_2vRgovXm75vgr81VvDMMyhahfLgkBztDircz5smMPjscBhuwLMNwLSSrlVa6oO_-QddxTqHMVyjZgBB1wwv1fku5FHNO2D-lYWB-VmdKdeZXdYV9-2f8J_J3VwU42gL3fsCH_5vM1_NvW-UPA3Ok5g</recordid><startdate>202302</startdate><enddate>202302</enddate><creator>Zhao, Shao‐Zhi</creator><creator>Zhao, Yu‐Xin</creator><creator>Liao, Xiao‐Hua</creator><creator>Huo, Ran</creator><creator>Li, Hao</creator><creator>Jiao, Yu‐Ming</creator><creator>Weng, Jian‐Cong</creator><creator>Wang, Jie</creator><creator>Liu, Bing</creator><creator>Cao, Yong</creator><general>Wiley Subscription Services, Inc</general><general>John Wiley and Sons Inc</general><scope>24P</scope><scope>WIN</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7QG</scope><scope>7QP</scope><scope>7QR</scope><scope>7TK</scope><scope>7U7</scope><scope>8FD</scope><scope>C1K</scope><scope>FR3</scope><scope>K9.</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0003-2029-5187</orcidid><orcidid>https://orcid.org/0000-0002-8289-1120</orcidid></search><sort><creationdate>202302</creationdate><title>Unruptured brain arteriovenous malformations causing seizures localize to one common brain network</title><author>Zhao, Shao‐Zhi ; 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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). 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.</abstract><cop>United States</cop><pub>Wiley Subscription Services, Inc</pub><pmid>36345215</pmid><doi>10.1002/jnr.25142</doi><tpages>11</tpages><orcidid>https://orcid.org/0000-0003-2029-5187</orcidid><orcidid>https://orcid.org/0000-0002-8289-1120</orcidid><oa>free_for_read</oa></addata></record> |
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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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