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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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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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 <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><identifier>ISSN: 0195-6108</identifier><identifier>EISSN: 1936-959X</identifier><identifier>DOI: 10.3174/ajnr.A5376</identifier><identifier>PMID: 28982784</identifier><language>eng</language><publisher>United States: American Society of Neuroradiology</publisher><subject>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</subject><ispartof>American journal of neuroradiology : AJNR, 2017-11, Vol.38 (11), p.2172-2179</ispartof><rights>2017 by American Journal of Neuroradiology.</rights><rights>Copyright American Society of Neuroradiology Nov 2017</rights><rights>2017 by American Journal of Neuroradiology 2017 American Journal of Neuroradiology</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c406t-8f129e90cb2f1129e74548533b499bded050e28021446f747cb6b67cec30b5783</citedby><cites>FETCH-LOGICAL-c406t-8f129e90cb2f1129e74548533b499bded050e28021446f747cb6b67cec30b5783</cites><orcidid>0000-0002-7349-7981 ; 0000-0001-5519-3135 ; 0000-0003-0678-1840 ; 0000-0003-4291-7346 ; 0000-0002-6726-3951 ; 0000-0002-9584-0576 ; 0000-0002-3787-1112 ; 0000-0002-9767-5156 ; 0000-0001-5209-3374 ; 0000-0001-6653-0774 ; 0000-0002-1041-8182 ; 0000-0002-4828-1687</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985237/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC5985237/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,723,776,780,881,27901,27902,53766,53768</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/28982784$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><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><title>Clinical and Imaging Characteristics of Arteriopathy Subtypes in Children with Arterial Ischemic Stroke: Results of the VIPS Study</title><title>American journal of neuroradiology : AJNR</title><addtitle>AJNR Am J Neuroradiol</addtitle><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 <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 & Calcified Tissue Abstracts</collection><collection>Neurosciences Abstracts</collection><collection>Technology Research Database</collection><collection>Engineering Research Database</collection><collection>Biotechnology and BioEngineering Abstracts</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>American journal of neuroradiology : AJNR</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Wintermark, M</au><au>Hills, N K</au><au>DeVeber, G A</au><au>Barkovich, A J</au><au>Bernard, T J</au><au>Friedman, N R</au><au>Mackay, M T</au><au>Kirton, A</au><au>Zhu, G</au><au>Leiva-Salinas, C</au><au>Hou, Q</au><au>Fullerton, H J</au><aucorp>VIPS Investigators</aucorp><aucorp>the VIPS Investigators</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Clinical and Imaging Characteristics of Arteriopathy Subtypes in Children with Arterial Ischemic Stroke: Results of the VIPS Study</atitle><jtitle>American journal of neuroradiology : AJNR</jtitle><addtitle>AJNR Am J Neuroradiol</addtitle><date>2017-11</date><risdate>2017</risdate><volume>38</volume><issue>11</issue><spage>2172</spage><epage>2179</epage><pages>2172-2179</pages><issn>0195-6108</issn><eissn>1936-959X</eissn><abstract>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 <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.</abstract><cop>United States</cop><pub>American Society of Neuroradiology</pub><pmid>28982784</pmid><doi>10.3174/ajnr.A5376</doi><tpages>8</tpages><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><oa>free_for_read</oa></addata></record> |
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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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