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Brain MRI in Progressive Supranuclear Palsy with Richardson's Syndrome and Variant Phenotypes.
Wattjes, Mike P; Huppertz, Hans-Jürgen; Mahmoudi, Nima; Stöcklein, Sophia; Rogozinski, Sophia; Wegner, Florian; Klietz, Martin; Apostolova, Ivayla; Levin, Johannes; Katzdobler, Sabrina; Buhmann, Carsten; Quattrone, Andrea; Berding, Georg; Brendel, Matthias; Barthel, Henryk; Sabri, Osama; Höglinger, Günter; Buchert, Ralph.
Afiliação
  • Wattjes MP; Department of Neuroradiology, Hannover Medical School, Hannover, Germany.
  • Huppertz HJ; Swiss Epilepsy Clinic, Klinik Lengg, Zurich, Switzerland.
  • Mahmoudi N; Department of Neuroradiology, Hannover Medical School, Hannover, Germany.
  • Stöcklein S; Department of Radiology, University Hospital of Munich, LMU Munich, Munich, Germany.
  • Rogozinski S; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Wegner F; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Klietz M; Department of Neurology, Hannover Medical School, Hannover, Germany.
  • Apostolova I; Department of Diagnostic and Interventional Radiology and Nuclear Medicine, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Levin J; Department of Neurology, University Hospital, LMU Munich, Munich, Germany.
  • Katzdobler S; German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
  • Buhmann C; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
  • Quattrone A; Department of Neurology, University Hospital, LMU Munich, Munich, Germany.
  • Berding G; German Center for Neurodegenerative Diseases (DZNE) Munich, Munich, Germany.
  • Brendel M; Munich Cluster for Systems Neurology (SyNergy), Munich, Germany.
  • Barthel H; Department of Neurology, University Medical Center Hamburg-Eppendorf, Hamburg, Germany.
  • Sabri O; Department of Neurology, University Hospital, LMU Munich, Munich, Germany.
  • Höglinger G; Institute of Neurology, Department of Medical and Surgical Sciences, University "Magna Graecia" of Catanzaro, Catanzaro, Italy.
  • Buchert R; Department of Nuclear Medicine, Hannover Medical School, Hannover, Germany.
Mov Disord ; 38(10): 1891-1900, 2023 10.
Article em En | MEDLINE | ID: mdl-37545102
ABSTRACT

BACKGROUND:

Brain magnetic resonance imaging (MRI) is used to support the diagnosis of progressive supranuclear palsy (PSP). However, the value of visual descriptive, manual planimetric, automatic volumetric MRI markers and fully automatic categorization is unclear, particularly regarding PSP predominance types other than Richardson's syndrome (RS).

OBJECTIVES:

To compare different visual reading strategies and automatic classification of T1-weighted MRI for detection of PSP in a typical clinical cohort including PSP-RS and (non-RS) variant PSP (vPSP) patients.

METHODS:

Forty-one patients (21 RS, 20 vPSP) and 46 healthy controls were included. Three readers using three strategies performed MRI

analysis:

exclusively visual reading using descriptive signs (hummingbird, morning-glory, Mickey-Mouse), visual reading supported by manual planimetry measures, and visual reading supported by automatic volumetry. Fully automatic classification was performed using a pre-trained support vector machine (SVM) on the results of atlas-based volumetry.

RESULTS:

All tested methods achieved higher specificity than sensitivity. Limited sensitivity was driven to large extent by false negative vPSP cases. Support by automatic volumetry resulted in the highest accuracy (75.1% ± 3.5%) among the visual strategies, but performed not better than the midbrain area (75.9%), the best single planimetric measure. Automatic classification by SVM clearly outperformed all other methods (accuracy, 87.4%), representing the only method to provide clinically useful sensitivity also in vPSP (70.0%).

CONCLUSIONS:

Fully automatic classification of volumetric MRI measures using machine learning methods outperforms visual MRI analysis without and with planimetry or volumetry support, particularly regarding diagnosis of vPSP, suggesting the use in settings with a broad phenotypic PSP spectrum. © 2023 The Authors. Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Supranuclear Progressiva / Encéfalo Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Paralisia Supranuclear Progressiva / Encéfalo Tipo de estudo: Guideline Limite: Humans Idioma: En Revista: Mov Disord Assunto da revista: NEUROLOGIA Ano de publicação: 2023 Tipo de documento: Article País de afiliação: Alemanha