Evidence map›Paper›PMID 42481001›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2026

Risk Factors for the Diagnosis of Progressive Supranuclear Palsy in the UK Biobank.

Charlie Weige Zhao, Marian Dale, Alexander Pantelyat, Maria Carmela Tartaglia, Ruth B Schneider, David G Coughlin, Federico Rodriguez-Porcel, Zbigniew Wszolek, Tao Xie, Lawrence I Golbe and 2 more

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

0numbers the graph read from it
0cells of the map it votes in
0citing papers in PubMed
–field-weighted citation impact
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

0 citing papers in PubMed.

No citing paper in PubMed yet.

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

12 authors.

Charlie Weige ZhaoDepartment of Neurology, Massachusetts General Brigham, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-8670-0985
Marian DaleDepartment of Neurology, Oregon Health and Science University, Portland, Oregon, USA.ORCID https://orcid.org/0000-0003-1010-982X
Alexander PantelyatDepartment of Neurology, Johns Hopkins University School of Medicine, Baltimore, Maryland, USA.ORCID https://orcid.org/0000-0002-6427-7485
Maria Carmela TartagliaTanz Centre for Research in Neurodegenerative Diseases, University of Toronto, Toronto, Ontario, Canada.
Ruth B SchneiderDepartment of Neurology and Center for Health & Technology, University of Rochester, Rochester, New York, USA.
David G CoughlinDepartment of Neurology, University of California San Diego, San Diego, California, USA.
Federico Rodriguez-PorcelDepartment of Neurology, Medical University of South Carolina, Charleston, South Carolina, USA.ORCID https://orcid.org/0000-0002-7492-5095
Zbigniew WszolekDepartment of Neurology, Mayo Clinic Florida, Jacksonville, Florida, USA.ORCID https://orcid.org/0000-0001-5487-1053
Tao XieDepartment of Neurology, University of Chicago Medicine, Chicago, Illinois, USA.
Lawrence I GolbeRutgers Robert Wood Johnson Medical School, New Brunswick, New Jersey, USA.
James B RoweDepartment of Clinical Neurosciences, MRC Cognition and Brain Sciences Unit, Cambridge, United Kingdom.ORCID https://orcid.org/0000-0001-7216-8679
Anne-Marie WillsDepartment of Neurology, Massachusetts General Brigham, Boston, Massachusetts, USA.ORCID https://orcid.org/0000-0002-0901-4711

Funding

Dolce family fund
6 · The paper itself

Abstract

backgroundProgressive supranuclear palsy (PSP) is a tauopathy for which there is limited understanding of epidemiological risk factors.

objectiveThe objective of this study was to identify premorbid nonmedical and medical risk factors for PSP diagnosis in a large prospective population-based cohort.

methodsWe performed a matched nested case-control study using the UK Biobank (UKB) cohort consisting of >500,000 adults aged 37 to 73 years. PSP diagnoses were identified from 2007 to censor date (August 2025) and matched 1:10 by age and sex to control subjects without parkinsonism or dementia diagnoses. We derived risk factors using an iterative logistic regression approach.

resultsThere were 240 incident PSP diagnoses in the UKB. In the fully adjusted model, premorbid depression (odds ratio [OR], 3.22; 95% confidence interval [CI], 2.30-4.50; P < 0.001), delirium (OR, 6.76; 95% CI, 4.08-11.19; P < 0.001), and functional gastrointestinal disorders (OR, 1.91; 95% CI, 1.39-2.63; P < 0.001) were associated with increased risk. Heavy alcohol consumption was associated with higher risk compared with moderate consumption (OR, 1.65; 95% CI: 1.21-2.26; P = 0.0017). Body mass index (BMI) and alcohol consumption had nonlinear risk profiles. Cancer diagnosis was inversely associated with PSP (OR, 0.56; 95% CI, 0.40-0.79; P < 0.001). Depression and delirium diagnoses remained significant 5 to 10 years before diagnosis.

conclusionsIn this large prospective cohort, PSP was associated with premorbid lifestyle practices and neuropsychiatric diagnoses years before diagnosis. This suggests a long premotor phase and highlights opportunities for earlier diagnosis and further mechanistic investigation. The inverse association with cancer mirrors the relationship seen in other neurodegenerative conditions and may point toward shared mechanisms. © 2026 International Parkinson and Movement Disorder Society.

Indexed as

Supranuclear Palsy, ProgressiveAdultAgedBiological Specimen BanksCase-Control StudiesCohort StudiesFemaleHumansMaleMiddle AgedProspective StudiesRisk FactorsUK BiobankUnited Kingdomatypical parkinsonismcase control studyepidemiologyprogressive supranuclear palsyrisk factors

Identifiers

PMID42481001
PMCPMC13387903

What Socratic holds

Textmetadata
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 Socratic graph.