Evidence map›Paper›PMID 40384451›Full record

ArticleMovement disorders clinical practice2025

Evaluating the Homogeneity of the PSP-RS Syndrome beyond Core Features.

Mahesh Kumar, Benjamin Brewer, Farwa Ali, Heather M Clark, Julie Stierwalt, Yehkyoung C Stephens, Rodolfo Savica, Dennis W Dickson, Jennifer L Whitwell, Keith A Josephs

Abstract read
In one paragraph

Article in Movement disorders clinical practice, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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1 · What the graph read from it

What it found

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2 · The registry

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3 · Its place in the literature

Who cites it

0 citing papers in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

10 authors.

Mahesh KumarDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0009-0002-8708-6726
Benjamin BrewerDepartment of Health Sciences Research (Biostatistics), Mayo Clinic, Rochester, MN, USA.
Farwa AliDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Heather M ClarkDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0001-9697-0084
Julie StierwaltDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Yehkyoung C StephensDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.
Rodolfo SavicaDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0002-2543-0627
Dennis W DicksonDepartment of Neuroscience, Mayo Clinic, Jacksonville, FL, USA.
Jennifer L WhitwellDepartment of Radiology, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0001-6914-1563
Keith A JosephsDepartment of Neurology, Mayo Clinic, Rochester, MN, USA.ORCID https://orcid.org/0000-0003-2930-8634

Funding

Longitudinal multi-modality imaging in progressive apraxia of speech (Diversity Supplement)R01DC012519 · NIDCD · MAYO CLINIC ROCHESTER · PI Jennifer Louise Whitwell · 2013 to 2026
$7.2M
Longitudinal Multi-modal Imaging in Progressive Supranuclear Palsy SyndromesR01NS089757 · NINDS · MAYO CLINIC ROCHESTER · PI JOSEPHS, KEITH A, WHITWELL, JENNIFER LOUISE · 2015 to 2024
$5.6M
The neurobiology of two distinct types of progressive apraxia of speechR01DC014942 · NIDCD · MAYO CLINIC ROCHESTER · PI Keith A Josephs, Rene Lynn Utianski · 2017 to 2026
$4.9M
Longitudinal multi-modal imaging in progressive supranuclear palsy syndromesR37NS089757 · NINDS · MAYO CLINIC ROCHESTER · PI Keith A Josephs, Jennifer Louise Whitwell · 2026 to 2026
$3.7M
NIDCD NIH HHS R01 DC012519NIDCD NIH HHS R01 DC014942NIDCD NIH HHS R01-DC12519NIDCD NIH HHS R01-DC14942NINDS NIH HHS R01 NS089757NINDS NIH HHS R01- NS89757NINDS NIH HHS R37 NS089757
6 · The paper itself

Abstract

backgroundClassic progressive supranuclear palsy RS syndrome (PSP-RS) is characterized by early postural instability/falls and vertical supranuclear gaze palsy, although other signs/symptoms can occur, for example, axial rigidity, bradykinesia, and cognitive dysfunction. The Movement Disorders Society-PSP (MDS-PSP) criteria consider probable PSP-RS a homogenous syndrome, but this has not been tested.

objectivesWe aim to investigate relationships between signs/symptoms of PSP-RS beyond its core features and determine whether PSP-RS is a homogeneous syndrome.

methods118 participants who met MDS-PSP criteria for probable PSP-RS were analyzed. All participants received an independent clinical diagnosis based on clinical judgment. We first performed a Network Analysis using qgraph with Spearman's correlation to quantify relationships between 16 signs/symptoms followed by a k-means clustering analysis using the same signs/symptoms to identify possible heterogeneity of the PSP-RS designation.

resultsFive network clusters were identified, reflecting: (1) tremor, (2) sensitivity to bright light, (3) oculomotor function, (4) cognition, and (5) akinetic-rigidity-praxis. Worse akinetic-rigidity was associated with better oculomotor function, but worse cognition. Cluster analysis revealed two clusters. Cluster I (n = 89) had more severe clinical features than Cluster II (n = 29). Cluster II had a higher frequency of participants (37.9%) clinically judged as not PSP-RS: these participants were less likely to have PSP pathology on autopsy (P = 0.03).

conclusionsSome signs/symptoms of PSP-RS strongly associate and are more likely to co-occur. PSP-RS, as defined by the MDS-PSP criteria includes a subset of participants not clinically judged as PSP-RS who are less likely to have PSP pathology.

Indexed as

Supranuclear Palsy, ProgressiveAgedAged, 80 and overCluster AnalysisFemaleHumansMaleMiddle AgedTremorclinical phenotypeshomogeneityPSP‐Richardson syndrome

Identifiers

PMID40384451
PMCPMC12528967

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Read under generation 80e0d062 · epoch 390. Bibliography from PubMed, PubMed Central and OpenAlex; grants from NIH RePORTER; trial links from ClinicalTrials.gov; estimates, votes and beliefs from the OpenQuestion graph.