Clinical and Imaging Characteristics of Arteriopathy Subtypes in Children with Arterial Ischemic Stroke: Results of the VIPS Study

Childhood arteriopathies are rare but heterogenous, and difficult to diagnose and classify, especially by nonexperts. We quantified clinical and imaging characteristics associated with childhood arteriopathy subtypes to facilitate their diagnosis and classification in research and clinical settings....

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Veröffentlicht in:American journal of neuroradiology : AJNR 2017-11, Vol.38 (11), p.2172-2179
Hauptverfasser: Wintermark, M, Hills, N K, DeVeber, G A, Barkovich, A J, Bernard, T J, Friedman, N R, Mackay, M T, Kirton, A, Zhu, G, Leiva-Salinas, C, Hou, Q, Fullerton, H J
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container_issue 11
container_start_page 2172
container_title American journal of neuroradiology : AJNR
container_volume 38
creator Wintermark, M
Hills, N K
DeVeber, G A
Barkovich, A J
Bernard, T J
Friedman, N R
Mackay, M T
Kirton, A
Zhu, G
Leiva-Salinas, C
Hou, Q
Fullerton, H J
description Childhood arteriopathies are rare but heterogenous, and difficult to diagnose and classify, especially by nonexperts. We quantified clinical and imaging characteristics associated with childhood arteriopathy subtypes to facilitate their diagnosis and classification in research and clinical settings. The Vascular Effects of Infection in Pediatric Stroke (VIPS) study prospectively enrolled 355 children with arterial ischemic stroke (2010-2014). A central team of experts reviewed all data to diagnose childhood arteriopathy and classify subtypes, including arterial dissection and focal cerebral arteriopathy-inflammatory type, which includes transient cerebral arteriopathy, Moyamoya disease, and diffuse/multifocal vasculitis. Only children whose stroke etiology could be conclusively diagnosed were included in these analyses. We constructed logistic regression models to identify characteristics associated with each arteriopathy subtype. Among 127 children with definite arteriopathy, the arteriopathy subtype could not be classified in 18 (14%). Moyamoya disease ( = 34) occurred mostly in children younger than 8 years of age; focal cerebral arteriopathy-inflammatory type ( = 25), in children 8-15 years of age; and dissection ( = 26), at all ages. Vertigo at stroke presentation was common in dissection. Dissection affected the cervical arteries, while Moyamoya disease involved the supraclinoid internal carotid arteries. A banded appearance of the M1 segment of the middle cerebral artery was pathognomonic of focal cerebral arteriopathy-inflammatory type but was present in
doi_str_mv 10.3174/ajnr.A5376
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We quantified clinical and imaging characteristics associated with childhood arteriopathy subtypes to facilitate their diagnosis and classification in research and clinical settings. The Vascular Effects of Infection in Pediatric Stroke (VIPS) study prospectively enrolled 355 children with arterial ischemic stroke (2010-2014). A central team of experts reviewed all data to diagnose childhood arteriopathy and classify subtypes, including arterial dissection and focal cerebral arteriopathy-inflammatory type, which includes transient cerebral arteriopathy, Moyamoya disease, and diffuse/multifocal vasculitis. Only children whose stroke etiology could be conclusively diagnosed were included in these analyses. We constructed logistic regression models to identify characteristics associated with each arteriopathy subtype. Among 127 children with definite arteriopathy, the arteriopathy subtype could not be classified in 18 (14%). Moyamoya disease ( = 34) occurred mostly in children younger than 8 years of age; focal cerebral arteriopathy-inflammatory type ( = 25), in children 8-15 years of age; and dissection ( = 26), at all ages. Vertigo at stroke presentation was common in dissection. Dissection affected the cervical arteries, while Moyamoya disease involved the supraclinoid internal carotid arteries. A banded appearance of the M1 segment of the middle cerebral artery was pathognomonic of focal cerebral arteriopathy-inflammatory type but was present in &lt;25% of patients with focal cerebral arteriopathy-inflammatory type; a small lenticulostriate distribution infarct was a more common predictor of focal cerebral arteriopathy-inflammatory type, present in 76%. It remained difficult to distinguish focal cerebral arteriopathy-inflammatory type from intracranial dissection of the anterior circulation. We observed only secondary forms of diffuse/multifocal vasculitis, mostly due to meningitis. 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We quantified clinical and imaging characteristics associated with childhood arteriopathy subtypes to facilitate their diagnosis and classification in research and clinical settings. The Vascular Effects of Infection in Pediatric Stroke (VIPS) study prospectively enrolled 355 children with arterial ischemic stroke (2010-2014). A central team of experts reviewed all data to diagnose childhood arteriopathy and classify subtypes, including arterial dissection and focal cerebral arteriopathy-inflammatory type, which includes transient cerebral arteriopathy, Moyamoya disease, and diffuse/multifocal vasculitis. Only children whose stroke etiology could be conclusively diagnosed were included in these analyses. We constructed logistic regression models to identify characteristics associated with each arteriopathy subtype. Among 127 children with definite arteriopathy, the arteriopathy subtype could not be classified in 18 (14%). Moyamoya disease ( = 34) occurred mostly in children younger than 8 years of age; focal cerebral arteriopathy-inflammatory type ( = 25), in children 8-15 years of age; and dissection ( = 26), at all ages. Vertigo at stroke presentation was common in dissection. Dissection affected the cervical arteries, while Moyamoya disease involved the supraclinoid internal carotid arteries. A banded appearance of the M1 segment of the middle cerebral artery was pathognomonic of focal cerebral arteriopathy-inflammatory type but was present in &lt;25% of patients with focal cerebral arteriopathy-inflammatory type; a small lenticulostriate distribution infarct was a more common predictor of focal cerebral arteriopathy-inflammatory type, present in 76%. It remained difficult to distinguish focal cerebral arteriopathy-inflammatory type from intracranial dissection of the anterior circulation. We observed only secondary forms of diffuse/multifocal vasculitis, mostly due to meningitis. Childhood arteriopathy subtypes have some typical features that aid diagnosis. Better imaging methods, including vessel wall imaging, are needed for improved classification of focal cerebral arteriopathy of childhood.</description><subject>Adolescent</subject><subject>Arteries</subject><subject>Brain Ischemia - diagnostic imaging</subject><subject>Brain Ischemia - etiology</subject><subject>Brain Ischemia - pathology</subject><subject>Carotid arteries</subject><subject>Carotid artery</subject><subject>Cerebral Arterial Diseases - complications</subject><subject>Cerebral Arterial Diseases - diagnostic imaging</subject><subject>Cerebral Arterial Diseases - pathology</subject><subject>Cerebral blood flow</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Children</subject><subject>Classification</subject><subject>Diagnosis</subject><subject>Dissection</subject><subject>Etiology</subject><subject>Female</subject><subject>Humans</subject><subject>Imaging</subject><subject>Infant</subject><subject>Inflammation</subject><subject>Ischemia</subject><subject>Male</subject><subject>Meningitis</subject><subject>Moyamoya disease</subject><subject>Pediatrics</subject><subject>Regression analysis</subject><subject>Regression models</subject><subject>Stroke</subject><subject>Stroke - diagnostic imaging</subject><subject>Stroke - etiology</subject><subject>Stroke - pathology</subject><subject>Studies</subject><subject>Vasculitis</subject><subject>Vertigo</subject><issn>0195-6108</issn><issn>1936-959X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpdkUFrFDEYhoModlu9-AMk4KUIU5NJMkk8CMuidaGguCreQiaT2ck6k6xJpmWv_vLOtGtRT18-voeHN7wAvMDogmBO3-idjxdLRnj1CCywJFUhmfzxGCwQlqyoMBIn4DSlHUKISV4-BSelkKLkgi7A71XvvDO6h9o3cD3orfNbuOp01Cbb6FJ2JsHQwmWc17DXuTvAzVjnw94m6PzEur6J1sMbl7sjNunWyXR2cAZucgw_7Vv4xaaxz3eu3Fn4ff15M93G5vAMPGl1n-zz4zwD3z68_7r6WFx9ulyvlleFoajKhWhxKa1Epi5bPD85ZVQwQmoqZd3YBjFkS4FKTGnVcspNXdUVN9YQVDMuyBl4d-_dj_VgG2N9jrpX--gGHQ8qaKf-vXjXqW24VkwKVhI-Cc6Pghh-jTZlNbhkbN9rb8OYFJZUcEYwYhP66j90F8bop-9NlJgIScmc6PU9ZWJIKdr2IQxGaq5WzdWqu2on-OXf8R_QP12SW7DVoQU</recordid><startdate>201711</startdate><enddate>201711</enddate><creator>Wintermark, M</creator><creator>Hills, N K</creator><creator>DeVeber, G A</creator><creator>Barkovich, A J</creator><creator>Bernard, T J</creator><creator>Friedman, N R</creator><creator>Mackay, M T</creator><creator>Kirton, A</creator><creator>Zhu, G</creator><creator>Leiva-Salinas, C</creator><creator>Hou, Q</creator><creator>Fullerton, H J</creator><general>American Society of Neuroradiology</general><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>7QO</scope><scope>7QP</scope><scope>7TK</scope><scope>8FD</scope><scope>FR3</scope><scope>P64</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-7349-7981</orcidid><orcidid>https://orcid.org/0000-0001-5519-3135</orcidid><orcidid>https://orcid.org/0000-0003-0678-1840</orcidid><orcidid>https://orcid.org/0000-0003-4291-7346</orcidid><orcidid>https://orcid.org/0000-0002-6726-3951</orcidid><orcidid>https://orcid.org/0000-0002-9584-0576</orcidid><orcidid>https://orcid.org/0000-0002-3787-1112</orcidid><orcidid>https://orcid.org/0000-0002-9767-5156</orcidid><orcidid>https://orcid.org/0000-0001-5209-3374</orcidid><orcidid>https://orcid.org/0000-0001-6653-0774</orcidid><orcidid>https://orcid.org/0000-0002-1041-8182</orcidid><orcidid>https://orcid.org/0000-0002-4828-1687</orcidid></search><sort><creationdate>201711</creationdate><title>Clinical and Imaging Characteristics of Arteriopathy Subtypes in Children with Arterial Ischemic Stroke: Results of the VIPS Study</title><author>Wintermark, M ; Hills, N K ; DeVeber, G A ; Barkovich, A J ; Bernard, T J ; Friedman, N R ; Mackay, M T ; Kirton, A ; Zhu, G ; Leiva-Salinas, C ; Hou, Q ; Fullerton, H J</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c406t-8f129e90cb2f1129e74548533b499bded050e28021446f747cb6b67cec30b5783</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Adolescent</topic><topic>Arteries</topic><topic>Brain Ischemia - diagnostic imaging</topic><topic>Brain Ischemia - etiology</topic><topic>Brain Ischemia - pathology</topic><topic>Carotid arteries</topic><topic>Carotid artery</topic><topic>Cerebral Arterial Diseases - complications</topic><topic>Cerebral Arterial Diseases - diagnostic imaging</topic><topic>Cerebral Arterial Diseases - pathology</topic><topic>Cerebral blood flow</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Children</topic><topic>Classification</topic><topic>Diagnosis</topic><topic>Dissection</topic><topic>Etiology</topic><topic>Female</topic><topic>Humans</topic><topic>Imaging</topic><topic>Infant</topic><topic>Inflammation</topic><topic>Ischemia</topic><topic>Male</topic><topic>Meningitis</topic><topic>Moyamoya disease</topic><topic>Pediatrics</topic><topic>Regression analysis</topic><topic>Regression models</topic><topic>Stroke</topic><topic>Stroke - diagnostic imaging</topic><topic>Stroke - etiology</topic><topic>Stroke - pathology</topic><topic>Studies</topic><topic>Vasculitis</topic><topic>Vertigo</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Wintermark, M</creatorcontrib><creatorcontrib>Hills, N K</creatorcontrib><creatorcontrib>DeVeber, G A</creatorcontrib><creatorcontrib>Barkovich, A J</creatorcontrib><creatorcontrib>Bernard, T J</creatorcontrib><creatorcontrib>Friedman, N R</creatorcontrib><creatorcontrib>Mackay, M T</creatorcontrib><creatorcontrib>Kirton, A</creatorcontrib><creatorcontrib>Zhu, G</creatorcontrib><creatorcontrib>Leiva-Salinas, C</creatorcontrib><creatorcontrib>Hou, Q</creatorcontrib><creatorcontrib>Fullerton, H J</creatorcontrib><creatorcontrib>VIPS Investigators</creatorcontrib><creatorcontrib>the VIPS Investigators</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Biotechnology Research Abstracts</collection><collection>Calcium &amp; 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We quantified clinical and imaging characteristics associated with childhood arteriopathy subtypes to facilitate their diagnosis and classification in research and clinical settings. The Vascular Effects of Infection in Pediatric Stroke (VIPS) study prospectively enrolled 355 children with arterial ischemic stroke (2010-2014). A central team of experts reviewed all data to diagnose childhood arteriopathy and classify subtypes, including arterial dissection and focal cerebral arteriopathy-inflammatory type, which includes transient cerebral arteriopathy, Moyamoya disease, and diffuse/multifocal vasculitis. Only children whose stroke etiology could be conclusively diagnosed were included in these analyses. We constructed logistic regression models to identify characteristics associated with each arteriopathy subtype. Among 127 children with definite arteriopathy, the arteriopathy subtype could not be classified in 18 (14%). Moyamoya disease ( = 34) occurred mostly in children younger than 8 years of age; focal cerebral arteriopathy-inflammatory type ( = 25), in children 8-15 years of age; and dissection ( = 26), at all ages. Vertigo at stroke presentation was common in dissection. Dissection affected the cervical arteries, while Moyamoya disease involved the supraclinoid internal carotid arteries. A banded appearance of the M1 segment of the middle cerebral artery was pathognomonic of focal cerebral arteriopathy-inflammatory type but was present in &lt;25% of patients with focal cerebral arteriopathy-inflammatory type; a small lenticulostriate distribution infarct was a more common predictor of focal cerebral arteriopathy-inflammatory type, present in 76%. It remained difficult to distinguish focal cerebral arteriopathy-inflammatory type from intracranial dissection of the anterior circulation. We observed only secondary forms of diffuse/multifocal vasculitis, mostly due to meningitis. 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source MEDLINE; Elektronische Zeitschriftenbibliothek - Frei zugängliche E-Journals; PubMed Central
subjects Adolescent
Arteries
Brain Ischemia - diagnostic imaging
Brain Ischemia - etiology
Brain Ischemia - pathology
Carotid arteries
Carotid artery
Cerebral Arterial Diseases - complications
Cerebral Arterial Diseases - diagnostic imaging
Cerebral Arterial Diseases - pathology
Cerebral blood flow
Child
Child, Preschool
Children
Classification
Diagnosis
Dissection
Etiology
Female
Humans
Imaging
Infant
Inflammation
Ischemia
Male
Meningitis
Moyamoya disease
Pediatrics
Regression analysis
Regression models
Stroke
Stroke - diagnostic imaging
Stroke - etiology
Stroke - pathology
Studies
Vasculitis
Vertigo
title Clinical and Imaging Characteristics of Arteriopathy Subtypes in Children with Arterial Ischemic Stroke: Results of the VIPS Study
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