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1000 Titel
  • Moyamoya disease in Southeast Asians: genetic and autopsy data, new cases, systematic review, and meta-analysis of all patients from the literature
1000 Autor/in
  1. Strunk, Daniel |
  2. Bauer, Peter |
  3. Keyvani, Kathy |
  4. Diehl, Rolf R. |
  5. Veltkamp, Roland |
  6. Berlit, Peter |
  7. Meuth, Sven G. |
  8. Timmermann, Lars |
  9. Schwitalla, Jan Claudius |
  10. Kraemer, Markus |
1000 Verlag Springer Berlin Heidelberg
1000 Erscheinungsjahr 2024
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2024-03-13
1000 Erschienen in
1000 Quellenangabe
  • 271(6):3328-3339
1000 Copyrightjahr
  • 2024
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00415-024-12228-0 |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC11136762/ |
1000 Publikationsstatus
1000 Begutachtungsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • <jats:title>Abstract</jats:title><jats:sec> <jats:title>Background</jats:title> <jats:p>Moyamoya disease (MMD) is a rare disorder causing ischemic and hemorrhagic juvenile stroke. It is associated with the founder susceptibility variant p.R4810K in the <jats:italic>RNF213</jats:italic> gene in East Asia. Our aim was to enhance understanding of MMD in so far poorly characterized Southeast Asians and exploring differences with Caucasian Europeans.</jats:p> </jats:sec><jats:sec> <jats:title>Methods</jats:title> <jats:p>By retrospective analysis of medical records and systematic database search on PubMed for all published cases, we identified Southeast Asian patients with MMD. We extracted and pooled proportions using fixed-effects models. Our own cohort was tested for the East Asian <jats:italic>RNF213</jats:italic> founder variant p.R4810K. One of our Southeast Asian patients underwent post-mortem histopathological examination.</jats:p> </jats:sec><jats:sec> <jats:title>Results</jats:title> <jats:p>The study cohort comprised 32 Southeast Asians. Mean age at onset in the entire cohort was 32.5 ± 20.3 years (<jats:italic>n</jats:italic> = 24), 43.4 ± 8.7 years in patients admitted to our center (<jats:italic>n</jats:italic> = 11), and 23.4 ± 22.4 years in patients from the international literature (<jats:italic>n</jats:italic> = 13). Female-to-male ratio was 1.6:1. MMD predominantly affected bilateral anterior intracranial vessels. Cerebral ischemia outnumbered transient ischemic attacks (TIAs) and intracranial hemorrhage. TIAs, arterial hypertension and obesity were significantly less frequent in Southeast Asian patients compared to Caucasian Europeans. p.R4810K was absent in all examined Southeast Asians despite of typical histopathological signs of MMD in one autopsy case.</jats:p> </jats:sec><jats:sec> <jats:title>Conclusion</jats:title> <jats:p>Clinical and histopathological manifestations of MMD in Southeast Asians are similar to those in Caucasian Europeans. The genotype of MMD in Southeast Asians differs from that of most East Asian patients.</jats:p> </jats:sec>
1000 Sacherschließung
lokal Moyamoya Disease/ethnology [MeSH]
lokal Asian People/genetics [MeSH]
lokal Ubiquitin-Protein Ligases/genetics [MeSH]
lokal White People [MeSH]
lokal Adenosine Triphosphatases/genetics [MeSH]
lokal East Asian
lokal Male [MeSH]
lokal East Asian People [MeSH]
lokal European People [MeSH]
lokal Asia, Southeastern [MeSH]
lokal Moyamoya Disease/genetics [MeSH]
lokal Adolescent [MeSH]
lokal Female [MeSH]
lokal Moyamoya Disease/pathology [MeSH]
lokal Adult [MeSH]
lokal Humans [MeSH]
lokal Retrospective Studies [MeSH]
lokal Middle Aged [MeSH]
lokal Histopathology
lokal Southeast Asian
lokal Southeast Asian People [MeSH]
lokal Young Adult [MeSH]
lokal European Caucasian
lokal Moyamoya disease
lokal Original Communication
lokal Asian People/ethnology [MeSH]
lokal Autopsy [MeSH]
1000 Fächerklassifikation (DDC)
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/U3RydW5rLCBEYW5pZWw=|https://frl.publisso.de/adhoc/uri/QmF1ZXIsIFBldGVy|https://frl.publisso.de/adhoc/uri/S2V5dmFuaSwgS2F0aHk=|https://frl.publisso.de/adhoc/uri/RGllaGwsIFJvbGYgUi4=|https://frl.publisso.de/adhoc/uri/VmVsdGthbXAsIFJvbGFuZA==|https://frl.publisso.de/adhoc/uri/QmVybGl0LCBQZXRlcg==|https://frl.publisso.de/adhoc/uri/TWV1dGgsIFN2ZW4gRy4=|https://frl.publisso.de/adhoc/uri/VGltbWVybWFubiwgTGFycw==|https://frl.publisso.de/adhoc/uri/U2Nod2l0YWxsYSwgSmFuIENsYXVkaXVz|https://orcid.org/0000-0002-5667-3621
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  1. Philipps-Universität Marburg |
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    1000 Förderer Philipps-Universität Marburg |
    1000 Förderprogramm -
    1000 Fördernummer -
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1000 Erstellt am 2025-07-05T08:56:45.045+0200
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