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Progressive Supranuclear Palsy: an Update

  • Movement Disorders (S Fox, Section Editor)
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Abstract

Purpose of review

Progressive supranuclear palsy (PSP) is a 4R tau neuropathologic entity. While historically defined by the presence of a vertical supranuclear gaze palsy and falls in the first symptomatic year, clinicopathologic studies identify alternate presenting phenotypes. This article reviews the new PSP diagnostic criteria, diagnostic approaches, and treatment strategies.

Recent findings

The 2017 International Parkinson and Movement Disorder Society PSP criteria outline 14 core clinical features and 4 clinical clues that combine to diagnose one of eight PSP phenotypes with probable, possible, or suggestive certainty. Evidence supports the use of select imaging approaches in the classic PSP-Richardson syndrome phenotype. Recent trials of putative disease-modifying agents showed no benefit.

Summary

The new PSP diagnostic criteria incorporating the range of presenting phenotypes have important implications for diagnosis and research. More work is needed to understand how diagnostic evaluations inform phenotype assessment and identify expected progression. Current treatment is symptomatic, but tau-based therapeutics are in active clinical trials.

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Authors and Affiliations

  1. Department of Neurology, University of Florida College of Medicine, Gainesville, FL, USA

    Melissa J. Armstrong

  2. Department of Neurology, University of Florida College of Medicine, McKnight Brain Institute, P.O. Box 100236, Gainesville, FL, 32610, USA

    Melissa J. Armstrong

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Armstrong, M.J. Progressive Supranuclear Palsy: an Update. Curr Neurol Neurosci Rep 18, 12 (2018). https://doi.org/10.1007/s11910-018-0819-5

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