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1000 Titel
  • CDKN2A deletion in supratentorial ependymoma with RELA alteration indicates a dismal prognosis: a retrospective analysis of the HIT ependymoma trial cohort
1000 Autor/in
  1. Jünger, Stephanie T. |
  2. Andreiuolo, Felipe |
  3. Mynarek, Martin |
  4. Wohlers, Inken |
  5. Rahmann, Sven |
  6. Klein-Hitpass, Ludger |
  7. Dörner, Evelyn |
  8. zur Mühlen, Anja |
  9. Velez-Char, Natalia |
  10. von Hoff, Katja |
  11. Warmuth-Metz, Monika |
  12. Kortmann, Rolf-Dieter |
  13. Timmermann, Beate |
  14. von Bueren, Andre |
  15. Rutkowski, Stefan |
  16. Pietsch, Torsten |
1000 Erscheinungsjahr 2020
1000 Publikationstyp
  1. Artikel |
1000 Online veröffentlicht
  • 2020-06-08
1000 Erschienen in
1000 Quellenangabe
  • 140(3):405-407
1000 Copyrightjahr
  • 2020
1000 Lizenz
1000 Verlagsversion
  • https://doi.org/10.1007/s00401-020-02169-z |
  • https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7423858/ |
1000 Publikationsstatus
1000 Sprache der Publikation
1000 Abstract/Summary
  • Progressive supranuclear palsy (PSP) is a 4R-tauopathy predominated by subcortical pathology in neurons, astrocytes, and oligodendroglia associated with various clinical phenotypes. In the present international study, we addressed the question of whether or not sequential distribution patterns can be recognized for PSP pathology. We evaluated heat maps and distribution patterns of neuronal, astroglial, and oligodendroglial tau pathologies and their combinations in different clinical subtypes of PSP in postmortem brains. We used conditional probability and logistic regression to model the sequential distribution of tau pathologies across different brain regions. Tau pathology uniformly predominates in the neurons of the pallido-nigro-luysian axis in different clinical subtypes. However, clinical subtypes are distinguished not only by total tau load but rather cell-type (neuronal versus glial) specific vulnerability patterns of brain regions suggesting distinct dynamics or circuit-specific segregation of propagation of tau pathologies. For Richardson syndrome (n = 81) we recognize six sequential steps of involvement of brain regions by the combination of cellular tau pathologies. This is translated to six stages for the practical neuropathological diagnosis by the evaluation of the subthalamic nucleus, globus pallidus, striatum, cerebellum with dentate nucleus, and frontal and occipital cortices. This system can be applied to further clinical subtypes by emphasizing whether they show caudal (cerebellum/dentate nucleus) or rostral (cortical) predominant, or both types of pattern. Defining cell-specific stages of tau pathology helps to identify preclinical or early-stage cases for the better understanding of early pathogenic events, has implications for understanding the clinical subtype-specific dynamics of disease-propagation, and informs tau-neuroimaging on distribution patterns.
1000 Sacherschließung
lokal Ependymoma/metabolism [MeSH]
lokal Cyclin-Dependent Kinase Inhibitor p16/deficiency [MeSH]
lokal Ependymoma/drug therapy [MeSH]
lokal Cyclin-Dependent Kinase Inhibitor p16/metabolism [MeSH]
lokal Humans [MeSH]
lokal Supratentorial Neoplasms/pathology [MeSH]
lokal Transcription Factor RelA/metabolism [MeSH]
lokal Ependymoma/pathology [MeSH]
lokal Cohort Studies [MeSH]
lokal Ependymoma/diagnosis [MeSH]
lokal Supratentorial Neoplasms/metabolism [MeSH]
lokal Prognosis [MeSH]
lokal Pathology
lokal Neurosciences
lokal Correspondence
1000 Liste der Beteiligten
  1. https://frl.publisso.de/adhoc/uri/SsO8bmdlciwgU3RlcGhhbmllIFQu|https://frl.publisso.de/adhoc/uri/QW5kcmVpdW9sbywgRmVsaXBl|https://frl.publisso.de/adhoc/uri/TXluYXJlaywgTWFydGlu|https://frl.publisso.de/adhoc/uri/V29obGVycywgSW5rZW4=|https://frl.publisso.de/adhoc/uri/UmFobWFubiwgU3Zlbg==|https://frl.publisso.de/adhoc/uri/S2xlaW4tSGl0cGFzcywgTHVkZ2Vy|https://frl.publisso.de/adhoc/uri/RMO2cm5lciwgRXZlbHlu|https://frl.publisso.de/adhoc/uri/enVyIE3DvGhsZW4sIEFuamE=|https://frl.publisso.de/adhoc/uri/VmVsZXotQ2hhciwgTmF0YWxpYQ==|https://frl.publisso.de/adhoc/uri/dm9uIEhvZmYsIEthdGph|https://frl.publisso.de/adhoc/uri/V2FybXV0aC1NZXR6LCBNb25pa2E=|https://frl.publisso.de/adhoc/uri/S29ydG1hbm4sIFJvbGYtRGlldGVy|https://frl.publisso.de/adhoc/uri/VGltbWVybWFubiwgQmVhdGU=|https://frl.publisso.de/adhoc/uri/dm9uIEJ1ZXJlbiwgQW5kcmU=|https://frl.publisso.de/adhoc/uri/UnV0a293c2tpLCBTdGVmYW4=|https://orcid.org/0000-0003-0763-6506
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  • DeepGreen-ID: 89f3db2b11a141038109ea20a4d35beb ; metadata provieded by: DeepGreen (https://www.oa-deepgreen.de/api/v1/), LIVIVO search scope life sciences (http://z3950.zbmed.de:6210/livivo), Crossref Unified Resource API (https://api.crossref.org/swagger-ui/index.html), to.science.api (https://frl.publisso.de/), ZDB JSON-API (beta) (https://zeitschriftendatenbank.de/api/), lobid - Dateninfrastruktur für Bibliotheken (https://lobid.org/resources/search)
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1000 Erstellt am 2023-11-16T23:22:09.316+0100
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1000 Zuletzt bearbeitet Fri Dec 01 04:17:34 CET 2023
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