Clinical diagnosis of progressive supranuclear palsy: The movement disorder society criteria

  • Günter U. Höglinger
    Department of Neurology Technische Universität München Munich Germany
  • Gesine Respondek
    Department of Neurology Technische Universität München Munich Germany
  • Maria Stamelou
    Second Department of Neurology Attikon University Hospital, University of Athens Athens Greece
  • Carolin Kurz
    Department of Psychiatry Ludwig‐Maximilians‐Universität Munich Germany
  • Keith A. Josephs
    Department of Neurology Mayo Clinic Rochester Minnesota USA
  • Anthony E. Lang
    Morton and Gloria Shulman Movement Disorders Clinic and the Edmond J. Safra Program in Parkinson's Disease Toronto Western Hospital Toronto Canada
  • Brit Mollenhauer
    Paracelsus‐Elena Klinik, Kassel, Germany, and University Medical Center Göttingen, Institute of Neuropathology Göttingen Germany
  • Ulrich Müller
    Institute of Human Genetics Giessen Germany
  • Christer Nilsson
    Department of Clinical Sciences, Division of Neurology Lund University Lund Sweden
  • Jennifer L. Whitwell
    Department of Radiology Mayo Clinic Rochester Minnesoya USA
  • Thomas Arzberger
    German Center for Neurodegenerative Diseases (DZNE) Munich Germany
  • Elisabet Englund
    Department of Clinical Sciences Division of Oncology and Pathology, Lund University Lund Sweden
  • Ellen Gelpi
    Neurological Tissue Bank of the Biobank ‐ Hospital Clínic de Barcelona Universitat de Barcelona, IDIBAPS Barcelona Spain
  • Armin Giese
    Center for Neuropathology and Prion Research Ludwig‐Maximilians‐Universität Munich Germany
  • David J. Irwin
    Frontotemporal Degeneration Center Department of Neurology, University of Pennsylvania Philadelphia Pennsylvania USA
  • Wassilios G. Meissner
    Université de Bordeaux, Institut des Maladies Neurodégénératives UMR 5293 Bordeaux France
  • Alexander Pantelyat
    Department of Neurology Johns Hopkins University Baltimore Maryland USA
  • Alex Rajput
    Division of Neurology Royal University Hospital, University of Saskatchewan Saskatoon SK Canada
  • John C. van Swieten
    Department of Neurology Erasmus Medical Centre Rotterdam The Netherlands
  • Claire Troakes
    London Neurodegenerative Diseases Brain Bank Institute of Psychiatry, Psychology and Neuroscience, Kings College London London United Kingdom
  • Angelo Antonini
    Parkinson and Movement Disorders Unit IRCCS Hospital San Camillo, Venice, and Department of Neurosciences, Padova University Padova Italy
  • Kailash P. Bhatia
    Sobell Department of Motor Neuroscience and Movement Disorders UCL Institute of Neurology Queen Square London United Kingdom
  • Yvette Bordelon
    Department of Neurology University of California Los Angeles California USA
  • Yaroslau Compta
    Parkinson's Disease & Movement Disorders Unit Neurology Service, Hospital Clinic/IDIBAPS/University of Barcelona Barcelona, Catalonia Spain
  • Jean‐Christophe Corvol
    Sorbonne Universités, UPMC Univ Paris 06; and INSERM UMRS_1127, CIC_1422; and CNRS UMR_7225; and AP‐HP; and ICM, Hôpital Pitié‐Salpêtrière, Département des maladies du système nerveux Paris France
  • Carlo Colosimo
    Department of Neurology Santa Maria University Hospital of Terni Terni Italy
  • Dennis W. Dickson
    Mayo Clinic Jacksonville Florida USA
  • Richard Dodel
    Department of Geriatric Medicine University Hospital Essen Essen Germany
  • Leslie Ferguson
    Division of Neurology Royal University Hospital, University of Saskatchewan Saskatoon SK Canada
  • Murray Grossman
    Frontotemporal Degeneration Center Department of Neurology, University of Pennsylvania Philadelphia Pennsylvania USA
  • Jan Kassubek
    Department of Neurology University of Ulm Ulm Germany
  • Florian Krismer
    Department of Neurology Medical University Innsbruck Innsbruck Austria
  • Johannes Levin
    German Center for Neurodegenerative Diseases (DZNE) Munich Germany
  • Stefan Lorenzl
    Institute of Nursing Science and Practice Paracelsus Medical University Salzburg Austria
  • Huw R. Morris
    Department of Clinical Neuroscience UCL Institute of Neurology London United Kingdom
  • Peter Nestor
    German Center for Neurodegenerative Diseases (DZNE) Magdeburg Germany
  • Wolfgang H. Oertel
    Department of Neurology Philipps Universität Marburg Germany
  • Werner Poewe
    Department of Neurology Medical University Innsbruck Innsbruck Austria
  • Gil Rabinovici
    Memory and Aging Center Department of Neurology, University of California San Francisco California USA
  • James B. Rowe
    Department of Clinical Neurosciences Cambridge University Cambridge United Kingdom
  • Gerard D. Schellenberg
    Department of Pathology and Laboratory Medicine Perelman School of Medicine, University of Pennsylvania Philadelphia Pennsylvania USA
  • Klaus Seppi
    Department of Neurology Medical University Innsbruck Innsbruck Austria
  • Thilo van Eimeren
    Departments of Nuclear Medicine and Neurology University of Cologne Cologne Germany
  • Gregor K. Wenning
    Department of Neurology Medical University Innsbruck Innsbruck Austria
  • Adam L. Boxer
    Memory and Aging Center Department of Neurology, University of California San Francisco California USA
  • Lawrence I. Golbe
    Department of Neurology Rutgers Robert Wood Johnson Medical School New Brunswick New Jersey USA
  • Irene Litvan
    Department of Neurology University of California San Diego California USA

書誌事項

公開日
2017-05-03
権利情報
  • http://onlinelibrary.wiley.com/termsAndConditions#vor
DOI
  • 10.1002/mds.26987
公開者
Wiley

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説明

<jats:title>ABSTRACT</jats:title><jats:p><jats:bold>Background</jats:bold>: PSP is a neuropathologically defined disease entity. Clinical diagnostic criteria, published in 1996 by the National Institute of Neurological Disorders and Stroke/Society for PSP, have excellent specificity, but their sensitivity is limited for variant PSP syndromes with presentations other than Richardson's syndrome.</jats:p><jats:p><jats:bold>Objective</jats:bold>: We aimed to provide an evidence‐ and consensus‐based revision of the clinical diagnostic criteria for PSP.</jats:p><jats:p><jats:bold>Methods</jats:bold>: We searched the PubMed, Cochrane, Medline, and PSYCInfo databases for articles published in English since 1996, using postmortem diagnosis or highly specific clinical criteria as the diagnostic standard. Second, we generated retrospective standardized clinical data from patients with autopsy‐confirmed PSP and control diseases. On this basis, diagnostic criteria were drafted, optimized in two modified Delphi evaluations, submitted to structured discussions with consensus procedures during a 2‐day meeting, and refined in three further Delphi rounds.</jats:p><jats:p><jats:bold>Results</jats:bold>: Defined clinical, imaging, laboratory, and genetic findings serve as mandatory basic features, mandatory exclusion criteria, or context‐dependent exclusion criteria. We identified four functional domains (ocular motor dysfunction, postural instability, akinesia, and cognitive dysfunction) as clinical predictors of PSP. Within each of these domains, we propose three clinical features that contribute different levels of diagnostic certainty. Specific combinations of these features define the diagnostic criteria, stratified by three degrees of diagnostic certainty (probable PSP, possible PSP, and suggestive of PSP). Clinical clues and imaging findings represent supportive features.</jats:p><jats:p><jats:bold>Conclusions</jats:bold>: Here, we present new criteria aimed to optimize early, sensitive, and specific clinical diagnosis of PSP on the basis of currently available evidence. © 2017 International Parkinson and Movement Disorder Society</jats:p>

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