Evidence map›Paper›PMID 41106089›Full record

ArticleParkinsonism & related disorders2025

Parkinson's disease mild cognitive impairment with MRI evidence of cholinergic nucleus 4 degeneration: A new subtype?

Ahmed Negida, Hiba Z Vohra, Sarah K Lageman, Nitai Mukhopadhyay, Brian D Berman, Daniel Weintraub, Matthew J Barrett

Abstract read
In one paragraph

Article in Parkinsonism & related disorders, 2025. 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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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

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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. Article
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4 · The record

Corrections and comments

5 · Who and what money

Authors and funding

7 authors.

Ahmed NegidaDepartment of Neurology, Virginia Commonwealth University, Richmond, VA, USA. Electronic address: ahmed.negida@vcuhealth.org.
Hiba Z VohraDepartment of Neurology, Virginia Commonwealth University, Richmond, VA, USA.
Sarah K LagemanDepartment of Neurology, Virginia Commonwealth University, Richmond, VA, USA.
Nitai MukhopadhyayDepartment of Biostatistics, Virginia Commonwealth University, Richmond, VA, USA.
Brian D BermanDepartment of Neurology, Virginia Commonwealth University, Richmond, VA, USA.
Daniel WeintraubDepartments of Psychiatry and Neurology, Perelman School of Medicine at the University of Pennsylvania, Parkinson's Disease Research, Education and Clinical Center (PADRECC), Philadelphia Veterans Affairs Medical Center, Philadelphia, PA, USA.
Matthew J BarrettDepartment of Neurology, Virginia Commonwealth University, Richmond, VA, USA.

Funding

Dystonia CoalitionU54NS065701 · NINDS · EMORY UNIVERSITY · PI JINNAH, HYDER A · 2009 to 2014
$7.0M
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 AG077469NINDS NIH HHS R01 NS142622NINDS NIH HHS U54 NS065701
6 · The paper itself

Abstract

backgroundSubtyping Parkinson's disease with mild cognitive impairment (PD-MCI) into clinically and pathologically homogeneous groups could improve clinical trials and enable personalized treatments. Cholinergic nucleus 4 (Ch4) degeneration has been linked to cognitive decline in PD, suggesting a distinct PD-MCI subtype with worse prognosis.

objectiveTo determine whether PD-MCI patients with MRI evidence of Ch4 degeneration exhibit a different clinical profile and cognitive trajectory than those without Ch4 degeneration.

methodsWe analyzed baseline MRI scans from 162 PD-MCI participants in the Parkinson's Progression Markers Initiative. Ch4 grey matter density (GMD) was assessed using voxel-based morphometry and probabilistic maps. Participants were classified as having low or normal Ch4 GMD using a z-score threshold of 1 SD below the mean. We compared clinical features and time to cognitive milestones using Kaplan-Meier survival analysis.

resultsOf 162 participants, 40 had low Ch4 GMD and 122 had normal Ch4 GMD. Those with low Ch4 GMD had significantly worse MDS-UPDRS total and subscale scores (II-III), greater autonomic dysfunction, and reduced olfaction (all P < 0.05). PD-MCI patients with low Ch4 GMD progressed faster to cognitive decline milestones (log-rank P = 0.0017). Subtyping PD-MCI patients by Ch4 GMD may provide more prognostic accuracy for capturing earlier cognitive progression compared to currently established PD subtypes.

conclusionPD-MCI patients with Ch4 degeneration may represent a distinct, clinically severe PD-MCI subtype with faster progression. This group may benefit from targeted inclusion in clinical trials, particularly those assessing cholinergic therapies.

Indexed as

Basal Nucleus of MeynertCognitive DysfunctionGray MatterNerve DegenerationParkinson DiseaseAgedDisease ProgressionFemaleHumansMagnetic Resonance ImagingMaleMiddle AgedCholinergic nucleiMild cognitive impairmentParkinson's diseaseSubtyping

Identifiers

PMID41106089
PMCPMC12949478

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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.