Evidence map›Paper›PMID 42286020›Full record

ArticleNPJ Parkinson's disease2026

Comparative analysis of progression milestones across Parkinson's disease clinical, pathological, and data-driven subtypes: a 10-year follow-up.

Ahmed Negida, Nitai Mukhopadhyay, Brian D Berman, Matthew J Barrett

Abstract read
In one paragraph

Article in NPJ Parkinson's disease, 2026. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 2 papers.

0numbers the graph read from it
0cells of the map it votes in
2citing papers in PubMed
–field-weighted citation impact
1 · What the graph read from it

What it found

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2 · The registry

The trial behind it

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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

2 citing papers in PubMed.

  1. Observational
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

4 authors.

Ahmed NegidaDepartment of Neurology, Virginia Commonwealth University, Richmond, VA, USA. ahmed.negida@vcuhealth.org.ORCID http://orcid.org/0000-0001-5363-6369
Nitai MukhopadhyayDepartment of Biostatistics, Virginia Commonwealth University, Richmond, VA, USA.
Brian D BermanDepartment of Neurology, Virginia Commonwealth University, Richmond, VA, USA.
Matthew J BarrettDepartment of Neurology, Virginia Commonwealth University, Richmond, VA, USA.

Funding

Elucidating the Role of Cholinergic Degeneration in Cognitive Fluctuations in Lewy Body DementiaR01NS142622 · NINDS · VIRGINIA COMMONWEALTH UNIVERSITY · PI Matthew James Barrett · 2025 to 2026
$1.4M
Development and characterization of EEG signature of cognitive fluctuations in Lewy body dementiaR21AG077469 · NIA · VIRGINIA COMMONWEALTH UNIVERSITY · PI BARRETT, MATTHEW JAMES, MUKHOPADHYAY, NITAI D. · 2022 to 2022
$427k
NIA NIH HHS R21 AG077469NIH HHS 1R21AG077469-01NINDS NIH HHS R01 NS142622
6 · The paper itself

Abstract

Parkinson's disease (PD) heterogeneity complicates disease-modification clinical trial design and lead to ambiguous results, necessitating robust subtyping frameworks to identify rapid progressors. This study compared progression milestones across previously defined clinical (tremor-dominant [TD], postural instability/gait difficulty [PIGD], indeterminate), pathological (brain-first, body-first), and data-driven (diffuse malignant [DM], intermediate [IM], mild motor-predominant [MMP]) PD subtypes. Using data from the Parkinson's Progression Markers Initiative (PPMI), we analyzed milestone attainment across six functional domains and performed Cox proportional hazards regression. Randomized controlled trial sample size simulations evaluated the impact of subtyping on trial efficiency. Data-driven subtypes exhibited the highest progression rates, with DM patients attaining 63.0% of milestones, surpassing PIGD (55.6%) and body-first (54.0%) subtypes. Cox proportional hazards regression confirmed that DM patients had the highest hazard of progression compared to MMP, after adjusting for age at enrollment. Trial power simulations demonstrated that enrolling DM patients could reduce sample size requirements by approximately 50% using standard trial durations compared to unstratified PD cohorts. This analysis showed that data-driven subtyping, particularly the identification of the DM subtype, offers a promising strategy to optimize disease-modification trials in PD by capturing patients who meet progression milestones earlier.

Identifiers

PMID42286020
PMCPMC13616926

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Registered trials

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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.