Evidence map›Paper›PMID 40353880›Full record

ReviewJournal of neural transmission (Vienna, Austria : 1996)2025

Neuroimaging in advanced Parkinson's disease: insights into pathophysiology, biomarkers, and personalized therapies.

Nils Schröter, Sergiu Groppa, Michel Rijntjes, Gabriel Gonzalez-Escamilla, Horst Urbach, Wolfgang H Jost, Alexander Rau

Abstract readReview
In one paragraph

Review in Journal of neural transmission (Vienna, Austria : 1996), 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 4 papers.

0numbers the graph read from it
0cells of the map it votes in
4citing 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

4 citing papers in PubMed.

  1. What's in a name? reframing advanced Parkinson's disease as a multidimensional state.Journal of neural transmission (Vienna, Austria : 1996) · 2026
    Review
  2. Article
  3. Article
  4. 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

7 authors.

Nils SchröterDepartment of Neurology, Saarland University Medical Center, Building 90, Kirrberger Straße, 66421, Homburg, Germany. nils.schroeter@uks.eu.ORCID 0000-0002-3833-9822
Sergiu GroppaDepartment of Neurology, Saarland University Medical Center, Building 90, Kirrberger Straße, 66421, Homburg, Germany.
Michel RijntjesDepartment of Neurology and Clinical Neuroscience, Medical Center, Faculty of Medicine, University of Freiburg, University of Freiburg, Freiburg, Germany.
Gabriel Gonzalez-EscamillaDepartment of Neurology, Saarland University Medical Center, Building 90, Kirrberger Straße, 66421, Homburg, Germany.
Horst UrbachDepartment of Neuroradiology, Medical Center, Faculty of Medicine, University of Freiburg, University of Freiburg, Freiburg, Germany.
Wolfgang H JostDepartment of Neurology, Saarland University Medical Center, Building 90, Kirrberger Straße, 66421, Homburg, Germany.
Alexander RauDepartment of Neuroradiology, Medical Center, Faculty of Medicine, University of Freiburg, University of Freiburg, Freiburg, Germany.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Advanced Parkinson's disease (APD) represents a late stage of Parkinson's disease and is characterized by complex motor and non-motor symptoms that are less responsive to oral dopaminergic therapies. While APD has a relevant impact on patients' quality of life and requires intensified treatment, consistent diagnostic criteria have only recently been proposed. The precise pathophysiology underlying the symptoms of APD remains poorly understood, making early prognostication and intervention difficult. Neuroimaging has emerged as a promising tool for elucidating the mechanisms driving APD, identifying biomarkers for disease staging, and predicting therapeutic response. Techniques such as molecular imaging and magnetic resonance imaging provide insight into molecular and structural changes associated with the progression of PD, including protein aggregation, neuroinflammation, and regional neurodegeneration. While positron emission tomography imaging of alpha-synuclein and other pathologies offers avenues for staging and differential diagnosis, advanced magnetic resonance imaging approaches have the potential for capturing subtle microstructural changes i.e. through neuromelanin-sensitive or diffusion-weighted imaging. However, the majority of imaging studies has focused on early Parkinson's disease, leaving their applicability to APD uncertain. Future research should prioritize the validation of neuroimaging findings in well-defined APD cohorts and extend their use to predict clinical milestones such as motor fluctuations, dyskinesia, and cognitive decline. These efforts are essential to advance personalized therapeutic strategies and bridge the gap between research and clinical management of APD.

Indexed as

NeuroimagingParkinson DiseasePrecision MedicineBiomarkersHumansBiomarkersAdvanced Parkinson’s diseaseImagingMRIPET

Identifiers

PMID40353880
PMCPMC12630204

What OpenQuestion holds

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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.