Evidence map›Paper›PMID 40415649›Full record

ArticleMovement disorders : official journal of the Movement Disorder Society2025

Distinct Longitudinal Clinical-Neuroanatomical Trajectories in Parkinson's Disease Clinical Subtypes: Insight toward Precision Medicine.

Seyed-Mohammad Fereshtehnejad, Roqaie Moqadam, Houman Azizi, Ronald B Postuma, Mahsa Dadar, Anthony E Lang, Connie Marras, Yashar Zeighami

Abstract read
In one paragraph

Article in Movement disorders : official journal of the Movement Disorder Society, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 11 papers.

0numbers the graph read from it
0cells of the map it votes in
11citing 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

11 citing papers in PubMed.

  1. Impulse Control Disorders Are Independent of Parkinson Disease Motor Subtypes.medRxiv : the preprint server for health sciences · 2026
    Article
  2. Review
  3. Article
  4. Clinical and Imaging Characteristics of Parkinson's Disease with Negative Alpha-Synuclein Seed Amplification Assay.Movement disorders : official journal of the Movement Disorder Society · 2026
    Article
  5. Article
  6. Review
  7. Article
  8. Article
  9. Article
  10. Article
  11. Review
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

8 authors.

Seyed-Mohammad FereshtehnejadDivision of Neurology, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.ORCID https://orcid.org/0000-0001-9255-9351
Roqaie MoqadamDouglas Mental Health University Institute, Department of Psychiatry, McGill University, Montreal, Quebec, Canada.
Houman AziziDouglas Mental Health University Institute, Department of Psychiatry, McGill University, Montreal, Quebec, Canada.
Ronald B PostumaDepartment of Neurology and Neurosurgery, Montreal Neurological Institute, McGill University, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0002-6468-4734
Mahsa DadarDouglas Mental Health University Institute, Department of Psychiatry, McGill University, Montreal, Quebec, Canada.
Anthony E LangDivision of Neurology, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.
Connie MarrasDivision of Neurology, Toronto Western Hospital, University of Toronto, Toronto, Ontario, Canada.
Yashar ZeighamiDouglas Mental Health University Institute, Department of Psychiatry, McGill University, Montreal, Quebec, Canada.ORCID https://orcid.org/0000-0002-0583-5811

Funding

CIHRFonds de Recherche du Québec - SantéHealthy Brains Healthy LivesNatural Sciences and Engineering Research Council of Canada
6 · The paper itself

Abstract

backgroundParkinson's disease (PD) varies widely across individuals in clinical manifestations and course of progression. Identification of distinct biological subtypes could explain this heterogeneity, identify its pathophysiology, and predict disease progression.

objectivesOur aim was to compare longitudinal clinical trajectories and brain atrophy patterns between clinical subtypes defined at the baseline de novo PD.

methodsWe analyzed data from 421 PD patients (mean follow-up: 8.2 years) in the Parkinson's Progression Markers Initiative (PPMI). Using multi-domain motor and non-motor criteria, de novo patients were classified into "mild motor-predominant" (n = 223), "intermediate" (n = 146), and "diffuse-malignant" (n = 52) subtypes. Deformation-based morphometry was performed on T1-weighted magnetic resonance imaging (MRIs) from 128 PD patients with at least two MRIs (71 mild motor-predominant, 42 intermediate, and 15 diffuse-malignant) and 60 controls, with an average MRI follow-up duration of 3.4 ± 1.1 in the PD cohort. Mixed-effects models compared clinical progression and longitudinal pattern of regional atrophy across subtypes.

resultsThe diffuse-malignant subtype exhibited faster worsening of motor severity (P = 0.007), cognition (P < 0.0001), and activities of daily living (P < 0.0001) compared to mild motor-predominant subtype over 8 years. These findings remained statistically significant after an age-matched subgroup analysis and adjustment for the levodopa treatment. Accelerated atrophy was observed in the precuneus, temporal and fusiform gyri, cerebellum, and other regions (corrected-P < 0.05).

conclusionsLongitudinal analysis revealed distinct patterns of clinical progression and regional atrophy in PD subtypes, with the diffuse-malignant subtype showing more severe neurodegeneration and clinical deterioration suggesting existence of diverse pathophysiological mechanisms in PD. © 2025 The Author(s). Movement Disorders published by Wiley Periodicals LLC on behalf of International Parkinson and Movement Disorder Society.

Indexed as

BrainParkinson DiseasePrecision MedicineAgedAtrophyDisease ProgressionFemaleHumansLongitudinal StudiesMagnetic Resonance ImagingMaleMiddle Agedbased morphometrydeformationlongitudinalmagnetic resonance imagingParkinson's diseasesubtype

Identifiers

PMID40415649
PMCPMC12371632

What OpenQuestion holds

Textmetadata
LicenceCC BY-NC-ND
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.