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Progression of initially unilateral Moyamoya angiopathy in Caucasian Europeans
Background Moyamoya angiopathy (MMA) is a rare cause of stroke in Caucasians, but it is much more frequent in East Asia. Since 2021, diagnostic criteria not only comprise bilateral, but also unilateral MMA. Hitherto, progression of unilateral MMA has predominantly been described in East Asians. Our...
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Published in: | Journal of neurology 2023-09, Vol.270 (9), p.4415-4422 |
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creator | Strunk, Daniel Diehl, Rolf R. Veltkamp, Roland Meuth, Sven G. Kraemer, Markus |
description | Background
Moyamoya angiopathy (MMA) is a rare cause of stroke in Caucasians, but it is much more frequent in East Asia. Since 2021, diagnostic criteria not only comprise bilateral, but also unilateral MMA. Hitherto, progression of unilateral MMA has predominantly been described in East Asians. Our study aimed to analyze the occurrence and characteristics of progression of initially unilateral MMA in Caucasian Europeans.
Methods
By retrospective analysis of medical records of 200 European Caucasians with MMA, admitted to our German center between 2010 and 2022, cases of unilateral MMA and its progression, i.e. progressive ipsi- or novel contralateral arterial stenosis, during follow-up were identified. Kruskal Wallis Test and Fisher’s Exact Test were used to identify statistically significant differences between progressive and stable patients concerning demographic, clinical, laboratory, and radiographic features.
Results
Our cohort comprised 63 patients with initially unilateral MMA. Fourteen (22.2%) had an ipsi- (
n
= 3, 21.4%) or contralateral (
n
= 11, 78.6%) progression. Mean age of patients with progressive MMA at symptom onset was 32 ± 14.1 years. The ratio of women to men in this subgroup was 2.5:1. Mean follow-up period was 5.4 ± 3.7 years, mean age at progression was 39.9 ± 12.7 years. Mean time interval between penultimate follow-up and progression was 4.8 ± 4.5 years. Patients with progression showed affection of the posterior cerebral artery (
p
= 0.009) and suffered from vertigo (
p
= 0.009) significantly more often.
Conclusion
Unilateral MMA progresses in a substantial proportion in European Caucasians. Long-term follow-up is required due to potential late progression with consecutive symptoms and the need for bypass surgery. |
doi_str_mv | 10.1007/s00415-023-11793-0 |
format | article |
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Moyamoya angiopathy (MMA) is a rare cause of stroke in Caucasians, but it is much more frequent in East Asia. Since 2021, diagnostic criteria not only comprise bilateral, but also unilateral MMA. Hitherto, progression of unilateral MMA has predominantly been described in East Asians. Our study aimed to analyze the occurrence and characteristics of progression of initially unilateral MMA in Caucasian Europeans.
Methods
By retrospective analysis of medical records of 200 European Caucasians with MMA, admitted to our German center between 2010 and 2022, cases of unilateral MMA and its progression, i.e. progressive ipsi- or novel contralateral arterial stenosis, during follow-up were identified. Kruskal Wallis Test and Fisher’s Exact Test were used to identify statistically significant differences between progressive and stable patients concerning demographic, clinical, laboratory, and radiographic features.
Results
Our cohort comprised 63 patients with initially unilateral MMA. Fourteen (22.2%) had an ipsi- (
n
= 3, 21.4%) or contralateral (
n
= 11, 78.6%) progression. Mean age of patients with progressive MMA at symptom onset was 32 ± 14.1 years. The ratio of women to men in this subgroup was 2.5:1. Mean follow-up period was 5.4 ± 3.7 years, mean age at progression was 39.9 ± 12.7 years. Mean time interval between penultimate follow-up and progression was 4.8 ± 4.5 years. Patients with progression showed affection of the posterior cerebral artery (
p
= 0.009) and suffered from vertigo (
p
= 0.009) significantly more often.
Conclusion
Unilateral MMA progresses in a substantial proportion in European Caucasians. Long-term follow-up is required due to potential late progression with consecutive symptoms and the need for bypass surgery.</description><identifier>ISSN: 0340-5354</identifier><identifier>EISSN: 1432-1459</identifier><identifier>DOI: 10.1007/s00415-023-11793-0</identifier><identifier>PMID: 37261501</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Adolescent ; Adult ; European People ; Female ; Humans ; Male ; Medical records ; Medicine ; Medicine & Public Health ; Middle Aged ; Moyamoya Disease - complications ; Moyamoya Disease - diagnostic imaging ; Neurology ; Neuroradiology ; Neurosciences ; Original Communication ; Patients ; Retrospective Studies ; Statistical analysis ; Stenosis ; Stroke ; White People ; Young Adult</subject><ispartof>Journal of neurology, 2023-09, Vol.270 (9), p.4415-4422</ispartof><rights>The Author(s), under exclusive licence to Springer-Verlag GmbH Germany 2023. Springer Nature or its licensor (e.g. a society or other partner) holds exclusive rights to this article under a publishing agreement with the author(s) or other rightsholder(s); author self-archiving of the accepted manuscript version of this article is solely governed by the terms of such publishing agreement and applicable law.</rights><rights>2023. The Author(s), under exclusive licence to Springer-Verlag GmbH Germany.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c326t-59b3b594c8ef6ca9f6708d4b980633a26521f05e445463efcbc62521dd78422c3</cites><orcidid>0000-0002-5667-3621</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37261501$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Strunk, Daniel</creatorcontrib><creatorcontrib>Diehl, Rolf R.</creatorcontrib><creatorcontrib>Veltkamp, Roland</creatorcontrib><creatorcontrib>Meuth, Sven G.</creatorcontrib><creatorcontrib>Kraemer, Markus</creatorcontrib><title>Progression of initially unilateral Moyamoya angiopathy in Caucasian Europeans</title><title>Journal of neurology</title><addtitle>J Neurol</addtitle><addtitle>J Neurol</addtitle><description>Background
Moyamoya angiopathy (MMA) is a rare cause of stroke in Caucasians, but it is much more frequent in East Asia. Since 2021, diagnostic criteria not only comprise bilateral, but also unilateral MMA. Hitherto, progression of unilateral MMA has predominantly been described in East Asians. Our study aimed to analyze the occurrence and characteristics of progression of initially unilateral MMA in Caucasian Europeans.
Methods
By retrospective analysis of medical records of 200 European Caucasians with MMA, admitted to our German center between 2010 and 2022, cases of unilateral MMA and its progression, i.e. progressive ipsi- or novel contralateral arterial stenosis, during follow-up were identified. Kruskal Wallis Test and Fisher’s Exact Test were used to identify statistically significant differences between progressive and stable patients concerning demographic, clinical, laboratory, and radiographic features.
Results
Our cohort comprised 63 patients with initially unilateral MMA. Fourteen (22.2%) had an ipsi- (
n
= 3, 21.4%) or contralateral (
n
= 11, 78.6%) progression. Mean age of patients with progressive MMA at symptom onset was 32 ± 14.1 years. The ratio of women to men in this subgroup was 2.5:1. Mean follow-up period was 5.4 ± 3.7 years, mean age at progression was 39.9 ± 12.7 years. Mean time interval between penultimate follow-up and progression was 4.8 ± 4.5 years. Patients with progression showed affection of the posterior cerebral artery (
p
= 0.009) and suffered from vertigo (
p
= 0.009) significantly more often.
Conclusion
Unilateral MMA progresses in a substantial proportion in European Caucasians. Long-term follow-up is required due to potential late progression with consecutive symptoms and the need for bypass surgery.</description><subject>Adolescent</subject><subject>Adult</subject><subject>European People</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Medical records</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Middle Aged</subject><subject>Moyamoya Disease - complications</subject><subject>Moyamoya Disease - diagnostic imaging</subject><subject>Neurology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Original Communication</subject><subject>Patients</subject><subject>Retrospective Studies</subject><subject>Statistical analysis</subject><subject>Stenosis</subject><subject>Stroke</subject><subject>White People</subject><subject>Young Adult</subject><issn>0340-5354</issn><issn>1432-1459</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><recordid>eNp9kLlOxDAQhi0EguV4AQoUiYYmMD4Tl2jFJS1HAbXleJ3Fq6y92EmRt8ewHBIFhTWS55t_Rh9CxxjOMUB1kQAY5iUQWmJcSVrCFppgRkmJGZfbaAKUQckpZ3toP6UlANS5sYv2aEUE5oAn6OEphkW0Kbngi9AWzrve6a4bi8G7Tvc26q64D6Ne5Vdov3BhrfvXMYPFVA9GJ6d9cTXEsLbap0O00-ou2aOveoBerq-ep7fl7PHmbno5Kw0loi-5bGjDJTO1bYXRshUV1HPWyBoEpZoITnAL3DLGmaC2NY0RJP_N51XNCDH0AJ1tctcxvA029WrlkrFdp70NQ1KkJlgwLKnM6OkfdBmG6PN1mWISVzlZZIpsKBNDStG2ah3dSsdRYVAfttXGtsq21adtBXno5Ct6aFZ2_jPyrTcDdAOk3PILG393_xP7DjNeiYU</recordid><startdate>20230901</startdate><enddate>20230901</enddate><creator>Strunk, Daniel</creator><creator>Diehl, Rolf R.</creator><creator>Veltkamp, Roland</creator><creator>Meuth, Sven G.</creator><creator>Kraemer, Markus</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</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>3V.</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>7X8</scope><orcidid>https://orcid.org/0000-0002-5667-3621</orcidid></search><sort><creationdate>20230901</creationdate><title>Progression of initially unilateral Moyamoya angiopathy in Caucasian Europeans</title><author>Strunk, Daniel ; Diehl, Rolf R. ; Veltkamp, Roland ; Meuth, Sven G. ; Kraemer, Markus</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c326t-59b3b594c8ef6ca9f6708d4b980633a26521f05e445463efcbc62521dd78422c3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>European People</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Medical records</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Middle Aged</topic><topic>Moyamoya Disease - complications</topic><topic>Moyamoya Disease - diagnostic imaging</topic><topic>Neurology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Original Communication</topic><topic>Patients</topic><topic>Retrospective Studies</topic><topic>Statistical analysis</topic><topic>Stenosis</topic><topic>Stroke</topic><topic>White People</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Strunk, Daniel</creatorcontrib><creatorcontrib>Diehl, Rolf R.</creatorcontrib><creatorcontrib>Veltkamp, Roland</creatorcontrib><creatorcontrib>Meuth, Sven G.</creatorcontrib><creatorcontrib>Kraemer, Markus</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>MEDLINE - Academic</collection><jtitle>Journal of neurology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Strunk, Daniel</au><au>Diehl, Rolf R.</au><au>Veltkamp, Roland</au><au>Meuth, Sven G.</au><au>Kraemer, Markus</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Progression of initially unilateral Moyamoya angiopathy in Caucasian Europeans</atitle><jtitle>Journal of neurology</jtitle><stitle>J Neurol</stitle><addtitle>J Neurol</addtitle><date>2023-09-01</date><risdate>2023</risdate><volume>270</volume><issue>9</issue><spage>4415</spage><epage>4422</epage><pages>4415-4422</pages><issn>0340-5354</issn><eissn>1432-1459</eissn><abstract>Background
Moyamoya angiopathy (MMA) is a rare cause of stroke in Caucasians, but it is much more frequent in East Asia. Since 2021, diagnostic criteria not only comprise bilateral, but also unilateral MMA. Hitherto, progression of unilateral MMA has predominantly been described in East Asians. Our study aimed to analyze the occurrence and characteristics of progression of initially unilateral MMA in Caucasian Europeans.
Methods
By retrospective analysis of medical records of 200 European Caucasians with MMA, admitted to our German center between 2010 and 2022, cases of unilateral MMA and its progression, i.e. progressive ipsi- or novel contralateral arterial stenosis, during follow-up were identified. Kruskal Wallis Test and Fisher’s Exact Test were used to identify statistically significant differences between progressive and stable patients concerning demographic, clinical, laboratory, and radiographic features.
Results
Our cohort comprised 63 patients with initially unilateral MMA. Fourteen (22.2%) had an ipsi- (
n
= 3, 21.4%) or contralateral (
n
= 11, 78.6%) progression. Mean age of patients with progressive MMA at symptom onset was 32 ± 14.1 years. The ratio of women to men in this subgroup was 2.5:1. Mean follow-up period was 5.4 ± 3.7 years, mean age at progression was 39.9 ± 12.7 years. Mean time interval between penultimate follow-up and progression was 4.8 ± 4.5 years. Patients with progression showed affection of the posterior cerebral artery (
p
= 0.009) and suffered from vertigo (
p
= 0.009) significantly more often.
Conclusion
Unilateral MMA progresses in a substantial proportion in European Caucasians. Long-term follow-up is required due to potential late progression with consecutive symptoms and the need for bypass surgery.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><pmid>37261501</pmid><doi>10.1007/s00415-023-11793-0</doi><tpages>8</tpages><orcidid>https://orcid.org/0000-0002-5667-3621</orcidid></addata></record> |
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subjects | Adolescent Adult European People Female Humans Male Medical records Medicine Medicine & Public Health Middle Aged Moyamoya Disease - complications Moyamoya Disease - diagnostic imaging Neurology Neuroradiology Neurosciences Original Communication Patients Retrospective Studies Statistical analysis Stenosis Stroke White People Young Adult |
title | Progression of initially unilateral Moyamoya angiopathy in Caucasian Europeans |
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