Evidence map›Paper›PMID 32383020›Full record

ArticleActa neuropathologica2020

Distribution patterns of tau pathology in progressive supranuclear palsy.

Gabor G Kovacs, Milica Jecmenica Lukic, David J Irwin, Thomas Arzberger, Gesine Respondek, Edward B Lee, David Coughlin, Armin Giese, Murray Grossman, Carolin Kurz and 13 more

Open access · hybridAbstract read
In one paragraph

Article in Acta neuropathologica, 2020. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 299 papers, 4 of them syntheses that pooled it.

0numbers the graph read from it
0cells of the map it votes in
299citing papers in PubMed, 4 pooled it
18.7field-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

299 citing papers in PubMed, 4 syntheses or guidelines pooled it, 449 citations in OpenAlex.

  1. Pooled it
  2. Pooled it
  3. 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
    Pooled it
  4. Pooled it
  5. Trial
  6. Article
  7. Article
  8. Dynamic [Molecular neurodegeneration · 2026
    Article
  9. Review
  10. Article
  11. Review
  12. Article
  13. Glymphatic dysfunction in cerebellar neurodegeneration: mechanistic insights and emerging clinical implications.Neurological sciences : official journal of the Italian Neurological Society and of the Italian Society of Clinical Neurophysiology · 2026
    Review
  14. Article
  15. Article
  16. Article
  17. A Brainstem Radiomics Framework to Distinguish Progressive Supranuclear Palsy from Parkinson's Disease.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  18. Article
  19. Article
  20. Article

239 more citing papers are in PubMed but not listed here.

4 · The record

Corrections and comments

PubMed lists nothing against this paper. Absence here is not a guarantee, only a check that was made.

5 · Who and what money

Authors and funding

23 authors at 12 institutions in 8 countries.

Gabor G KovacsCenter for Neurodegenerative Disease Research (CNDR), Institute On Aging and Department of Pathology & Laboratory Medicine, University of Pennsylvania, 3600 Spruce Street, 3 Maloney Building, Philadelphia, PA, 19104-4283, USA. gabor.kovacs@uhnresearch.ca.ORCID http://orcid.org/0000-0003-3841-5511
Milica Jecmenica LukicGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
David J IrwinDepartment of Neurology, University of Pennsylvania, Philadelphia, USA.
Thomas ArzbergerGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Gesine RespondekGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Edward B LeeCenter for Neurodegenerative Disease Research (CNDR), Institute On Aging and Department of Pathology & Laboratory Medicine, University of Pennsylvania, 3600 Spruce Street, 3 Maloney Building, Philadelphia, PA, 19104-4283, USA.
David CoughlinFrontotemporal Degeneration Center, University of Pennsylvania, Philadelphia, USA.ORCID https://orcid.org/0000-0003-4111-0102
Armin GieseCenter for Neuropathology and Prion Research, LMU Munich, Munich, Germany.
Murray GrossmanDepartment of Neurology, University of Pennsylvania, Philadelphia, USA.
Carolin KurzGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany.
Corey T McMillanDepartment of Neurology, University of Pennsylvania, Philadelphia, USA.
Ellen GelpiNeurological Tissue Bank and Neurology Department, Hospital Clínic de Barcelona, Universitat de Barcelona, IDIBAPS, CERCA, Barcelona, Catalonia, Spain.
Yaroslau ComptaParkinson's Disease & Movement Disorders Unit, Hospital Clínic / IDIBAPS / CIBERNED (CB06/05/0018-ISCIII) / European Reference Network for Rare Neurological Diseases (ERN-RND) / Institut de Neurociències (Maria de Maeztu Center), Universitat de Barcelona, Barcelona, Catalonia, Spain.
John C van SwietenDepartment of Neurology, Erasmus Medical Centre, Rotterdam, The Netherlands.
Laura Donker LaatDepartment Clinical Genetics, Erasmus Medical Center, Rotterdam, The Netherlands.
Claire TroakesLondon Neurodegenerative Diseases Brain Bank, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London, UK.
Safa Al-SarrajLondon Neurodegenerative Diseases Brain Bank, Institute of Psychiatry, Psychology and Neuroscience, Kings College London, London, UK.
John L RobinsonCenter for Neurodegenerative Disease Research (CNDR), Institute On Aging and Department of Pathology & Laboratory Medicine, University of Pennsylvania, 3600 Spruce Street, 3 Maloney Building, Philadelphia, PA, 19104-4283, USA.
Sigrun RoeberCenter for Neuropathology and Prion Research, LMU Munich, Munich, Germany.
Sharon X XieDepartment of Biostatistics, Epidemiology and Informatics, University of Pennsylvania, Philadelphia, USA.
Virginia M-Y LeeCenter for Neurodegenerative Disease Research (CNDR), Institute On Aging and Department of Pathology & Laboratory Medicine, University of Pennsylvania, 3600 Spruce Street, 3 Maloney Building, Philadelphia, PA, 19104-4283, USA.
John Q TrojanowskiCenter for Neurodegenerative Disease Research (CNDR), Institute On Aging and Department of Pathology & Laboratory Medicine, University of Pennsylvania, 3600 Spruce Street, 3 Maloney Building, Philadelphia, PA, 19104-4283, USA. trojanow@upenn.edu.
Günter U HöglingerGerman Center for Neurodegenerative Diseases (DZNE), Munich, Germany. guenter.hoeglinger@dzne.de.
German Center for Neurodegenerative Diseases · DEUniversity of Pennsylvania · USInstitute on Aging · USKing's College London · GBLudwig-Maximilians-Universität München · DEErasmus MC · NLErasmus University Rotterdam · NLHospital Clínic de Barcelona · ESInstitute for Neurodegenerative Disorders · USInstituto de Salud Carlos III · ESUniversity Health Network · CAUniversity of California San Diego · US

Funding

Transgenic Mouse Models of Tau PathologiesP01AG017586 · NIA · UNIVERSITY OF PENNSYLVANIA · PI LEE, VIRGINIA M · 2000 to 2021
$37.3M
UPenn ADCC Biomarker CoreP30AG010124 · NIA · UNIVERSITY OF PENNSYLVANIA · PI XIE, SHARON XIANGWEN · 1991 to 2020
$35.1M
Understanding Environmental Contributions to Heterogeneity in bvFTD.P01AG066597 · NIA · UNIVERSITY OF PENNSYLVANIA · PI David John Irwin, Corey T McMillan · 2020 to 2026
$18.8M
Project IV "Tackling Heterogeneity of Cognitive Trajectory in LBD"U19AG062418 · NIA · UNIVERSITY OF PENNSYLVANIA · PI TROJANOWSKI, JOHN Q. · 2019 to 2023
$18.1M
NRSA Training CoreTL1TR001880 · NCATS · UNIVERSITY OF PENNSYLVANIA · PI MEAGHER, EMMA ANNE · 2016 to 2025
$10.0M
Microscopic and Large-Scale Networks of Molecular Pathology in Frontotemporal Lobar DegenerationR01NS109260 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI IRWIN, DAVID JOHN · 2019 to 2023
$3.8M
Identification of Endophenotypes in the Behavioral-Variant of Frontotemporal DemeK23NS088341 · NINDS · UNIVERSITY OF PENNSYLVANIA · PI IRWIN, DAVID JOHN · 2014 to 2018
$836k
Medical Research Council MR/L016397/1NCATS NIH HHS TL1 TR001880NIA NIH HHS P01 AG017586NIA NIH HHS P01 AG066597NIA NIH HHS P30 AG010124NIA NIH HHS U19 AG062418NINDS NIH HHS K23 NS088341NINDS NIH HHS R01 NS109260
6 · The paper itself

Abstract

Progressive supranuclear palsy (PSP) is a 4R-tauopathy predominated by subcortical pathology in neurons, astrocytes, and oligodendroglia associated with various clinical phenotypes. In the present international study, we addressed the question of whether or not sequential distribution patterns can be recognized for PSP pathology. We evaluated heat maps and distribution patterns of neuronal, astroglial, and oligodendroglial tau pathologies and their combinations in different clinical subtypes of PSP in postmortem brains. We used conditional probability and logistic regression to model the sequential distribution of tau pathologies across different brain regions. Tau pathology uniformly predominates in the neurons of the pallido-nigro-luysian axis in different clinical subtypes. However, clinical subtypes are distinguished not only by total tau load but rather cell-type (neuronal versus glial) specific vulnerability patterns of brain regions suggesting distinct dynamics or circuit-specific segregation of propagation of tau pathologies. For Richardson syndrome (n = 81) we recognize six sequential steps of involvement of brain regions by the combination of cellular tau pathologies. This is translated to six stages for the practical neuropathological diagnosis by the evaluation of the subthalamic nucleus, globus pallidus, striatum, cerebellum with dentate nucleus, and frontal and occipital cortices. This system can be applied to further clinical subtypes by emphasizing whether they show caudal (cerebellum/dentate nucleus) or rostral (cortical) predominant, or both types of pattern. Defining cell-specific stages of tau pathology helps to identify preclinical or early-stage cases for the better understanding of early pathogenic events, has implications for understanding the clinical subtype-specific dynamics of disease-propagation, and informs tau-neuroimaging on distribution patterns.

Indexed as

tau ProteinsAgedBrainCohort StudiesFemaleHumansMaleMiddle AgedSupranuclear Palsy, ProgressiveMAPT protein, humantau ProteinsCoiled bodyNeurofibrillary tangleProgressive supranuclear palsyPropagationRichardson syndromeSequential involvementStageTauTauopathyTufted astrocyte

Identifiers

PMID32383020
PMCPMC7360645
OpenAlexW3022376055

What OpenQuestion holds

Textmetadata
LicenceCC BY
Read underepoch 390

Registered trials

None linked

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.