Evidence map›Paper›PMID 30726566›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2019

Sensitivity and Specificity of Diagnostic Criteria for Progressive Supranuclear Palsy.

Farwa Ali, Peter R Martin, Hugo Botha, J Eric Ahlskog, James H Bower, Joseph Y Masumoto, Demetrius Maraganore, Anhar Hassan, Scott Eggers, Bradley F Boeve and 9 more

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2019. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 97 papers, 3 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
97citing papers in PubMed, 3 pooled it
11.6field-weighted citation impact, top 1% of its field
1 · What the graph read from it

What it found

Each row is one number read from the abstract, on the scale the paper reported it, with its interval. Left of the dashed line favours the treatment, right favours the comparator. Under each row is the sentence it came from. New to these charts? A ten-minute tutorial.

The abstract states no effect estimate the extractor could read, or names no intervention and outcome on the map, so this paper lights no cell and moves no belief. It is still indexed, cited and linked below.

2 · The registry

The trial behind it

Trials whose registry record cites this paper, or whose number appears in the abstract. A trial that started after this paper was published is citing it as background, not reporting it.

Neither the registry nor the abstract names a trial number. If this is a trial report, that itself is worth knowing.

3 · Its place in the literature

Who cites it

97 citing papers in PubMed, 3 syntheses or guidelines pooled it, 142 citations in OpenAlex.

  1. Differentiating progressive supranuclear palsy from other movement disorders using transcranial sonography: a systematic review and meta-analysis.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2024
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  19. Bedside Assessment of Downgaze Limit by Amplitude.Movement disorders clinical practice · 2025
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37 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

19 authors at 6 institutions in 1 country.

Farwa AliDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Peter R MartinDepartment of Biostatistics, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Hugo BothaDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
J Eric AhlskogDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
James H BowerDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Joseph Y MasumotoUnniversity of Minnesota, Minneapolis, Minnesota, USA.
Demetrius MaraganoreUniversity of Florida, Gainesville, Florida, USA.
Anhar HassanDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Scott EggersDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Bradley F BoeveDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
David S KnopmanDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Daniel DrubachDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Ronald C PetersenDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Erika Driver DunkleyDepartment of Neurology, Mayo Clinic Arizona, Phoenix, Arizona, USA.
Jay van GerpenDepartment of Neurology, Mayo Clinic Arizona, Phoenix, Arizona, USA.
Ryan UittiDepartment of Neurology, Mayo Clinic Florida, Jacksonville, Florida, USA.
Jennifer L WhitwellDepartment of Radiology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Dennis W DicksonDepartment of Neuroscience, Mayo Clinic Florida, Jacksonville, Florida, USA.
Keith A JosephsDepartment of Neurology, Mayo Clinic Rochester, Rochester, Minnesota, USA.
Mayo Clinic · USJacksonville College · USMayo Clinic Hospital · USMayo Clinic in Florida · USUniversity of Florida · USUniversity of Minnesota · US

Funding

SUPPLEMENT TO ALZHEIMERS DISEASE PATIENT REGISTRYU01AG006786 · NIA · MAYO CLINIC ROCHESTER · PI GRAFF-RADFORD, JONATHAN, JACK, CLIFFORD R. · 1986 to 2023
$49.6M
THE PGRN/TDP-43 AXIS IN ALZHEIMER?S DISEASE AND NEURODEGENERATIONP50AG016574 · NIA · MAYO CLINIC ROCHESTER · PI BU, GUOJUN · 1999 to 2018
$36.9M
Research Education ComponentP30AG062677 · NIA · MAYO CLINIC ROCHESTER · PI Walter K. Kremers · 2019 to 2026
$33.5M
Longitudinal Imaging Biomarkers of Prodromal DLBU01NS100620 · NINDS · MAYO CLINIC ROCHESTER · PI Bradley F Boeve, KEJAL KANTARCI · 2017 to 2026
$19.2M
The Four Repeat Tauopathy Neuroimaging InitiativeR01AG038791 · NIA · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOXER, ADAM L. · 2010 to 2020
$18.1M
Longitudinal Evaluation of Familial Frontotemporal Dementia Subjects (LEFFTDS)U01AG045390 · NIA · MAYO CLINIC ROCHESTER · PI BOEVE, BRADLEY F, ROSEN, HOWARD J · 2014 to 2018
$16.9M
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
Training - The Frontotemporal Lobar Degeneration Clinical Research ConsortiumU54NS092089 · NINDS · UNIVERSITY OF CALIFORNIA, SAN FRANCISCO · PI BOXER, ADAM L. · 2014 to 2018
$6.4M
Connectomic imaging in familial and sporadic frontotemporal degenerationU01AG052943 · NIA · UNIVERSITY OF PENNSYLVANIA · PI GORNO TEMPINI, MARIA LUISA, GROSSMAN, MURRAY · 2016 to 2019
$5.9M
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
Multi-site longitudinal Integrated Neurocognitive and Sleep-Behavior Profiler for the Endophenotypic Classification of Dementia Subtypes (INSPECDS)R44AG050326 · NIA · ADVANCED BRAIN MONITORING, INC. · PI BERKA, CHRIS · 2016 to 2024
$4.4M
Epidemiology of Familial Late-Onset Alzheimer's DiseaseR01AG041797 · NIA · COLUMBIA UNIVERSITY HEALTH SCIENCES · PI MAYEUX, RICHARD P · 2012 to 2016
$4.2M
NIA NIH HHS P30 AG062677NIA NIH HHS P50 AG016574NIA NIH HHS R01 AG038791NIA NIH HHS R01 AG041797NIA NIH HHS R34 AG056639NIA NIH HHS R44 AG050326NIA NIH HHS R44 AG054256NIA NIH HHS U01 AG006786NIA NIH HHS U01 AG045390NIA NIH HHS U01 AG052943NIDCD NIH HHS R01 DC010367NIDCD NIH HHS R01 DC012519NINDS NIH HHS R01 NS089757NINDS NIH HHS R21 NS094684NINDS NIH HHS U01 NS100620NINDS NIH HHS U54 NS092089
6 · The paper itself

Abstract

backgroundIn 2017, the International Parkinson and Movement Disorder Society put forward new clinical criteria for the diagnosis of PSP, recognizing diverse PSP phenotypes. In this study, we compared the sensitivity and specificity of the new criteria with the National Institutes of Neurological Disease and Society for Progressive Supranuclear Palsy criteria at different times.

methodsPatients with clinical parkinsonism, clinical and/or neuropathological diagnosis of PSP, were identified from the Society for Progressive Supranuclear Palsy brain bank. All patients had neuropathologic diagnoses and detailed clinical examination performed by a neurologist at 1 of the 3 Mayo Clinic sites, in Florida, Arizona, and Minnesota. Clinical symptoms and signs were abstracted retrospectively in a blinded fashion and used to determine whether patients met either diagnostic criterion. Patients were divided into early and late disease stage groups using a 3-year cutoff.

resultsA total of 129 patients were included, of whom 66 had PSP pathology (51%). The remainder had other neurodegenerative diseases. The overall sensitivity of the International Parkinson and Movement Disorder Society criteria was 87.9%, compared with 45.5% for the National Institutes of Neurological Disease and Society for Progressive Supranuclear Palsy criteria, whereas the specificity of the International Parkinson and Movement Disorder Society probable PSP criteria was 85.7%, compared with 90.5% for the National Institutes of Neurological Disease and Society for Progressive Supranuclear Palsy. Individual patients were noted to have features of multiple PSP phenotypes.

conclusionThe International Parkinson and Movement Disorder Society criteria recognize several phenotypes of progressive supranuclear palsy and hence have higher sensitivity than the previous criteria. © 2019 International Parkinson and Movement Disorder Society.

Indexed as

Biological Specimen BanksBrainCognitive DysfunctionFemaleFrontotemporal Lobar DegenerationHumansLewy Body DiseaseMaleMultiple System AtrophyParkinsonian DisordersPostural BalanceSensation DisordersSensitivity and SpecificitySupranuclear Palsy, ProgressiveTauopathiesMDS-PSPNINDS-SPSPprogressive supranuclear palsyPSP diagnostic criteria

Identifiers

PMID30726566
PMCPMC6688972
OpenAlexW2913385104

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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.