Evidence map›Paper›PMID 40739885›Full record

ArticleJournal of Parkinson's disease2025

Progression to Parkinson's dementia is not modulated by genetic risk variants for Alzheimer's or Parkinson's disease.

Kayenat Parveen, J Alexander Ross, Hendrik van der Wurp, Monika Balzer-Geldsetzer, Daniela Berg, Günther Deuschl, Thomas Gasser, Rüdiger Hilker-Roggendorf, Elke Kalbe, Inga Liepelt-Scarfone and 13 more

Abstract read
In one paragraph

Article in Journal of Parkinson's disease, 2025. 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

23 authors.

Kayenat ParveenDivision of Neurogenetics and Molecular Psychiatry, Department of Psychiatry and Psychotherapy, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.
J Alexander RossDepartment of Geriatric Medicine and Center for Translational and Behavioral Neuroscience, University Duisburg-Essen, Essen, Germany.ORCID 0000-0001-9286-2748
Hendrik van der WurpDepartment of Geriatric Medicine and Center for Translational and Behavioral Neuroscience, University Duisburg-Essen, Essen, Germany.ORCID 0000-0002-1044-417X
Monika Balzer-GeldsetzerDepartment of Neurology, Philipps University Marburg, Marburg, Germany.
Daniela BergDepartment of Neurology, Christian Albrechts University, Kiel, Germany.ORCID 0000-0001-5796-5442
Günther DeuschlDepartment of Neurology, Christian Albrechts University, Kiel, Germany.ORCID 0000-0002-4176-9196
Thomas GasserDepartment of Neurodegenerative Diseases, Hertie Institute for Clinical Brain Research and German Center for Neurodegenerative Diseases (DZNE), University Tübingen, and German Center for Neurodegenerative Diseases, Tübingen, Germany.ORCID 0000-0002-1069-1146
Rüdiger Hilker-RoggendorfDepartment of Neurology, J.W. Goethe University, Frankfurt/Main, Germany.
Elke KalbeMedical Psychology, Neuropsychology, Gender Studies & Centre for Neuropsychological Diagnostics and Intervention (CeNDI), Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.ORCID 0000-0001-8603-2545
Inga Liepelt-ScarfoneDepartment of Parkinson, Sleep and Movement Disorders, Centre of Neurology, University Hospital Bonn and German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.
Brit MollenhauerParacelsus-Elena Clinic, Centre of Parkinsonism and Movement Disorders, Kassel, Germany.
Oliver RiedelLeibniz Institute for Prevention Research and Epidemiology, Bremen, Germany.ORCID 0000-0002-1721-502X
Sandra RöskeDepartment of Parkinson, Sleep and Movement Disorders, Centre of Neurology, University Hospital Bonn and German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.ORCID 0000-0002-8262-4356
Jörg B SchulzDepartment of Neurology, Medical Faculty, RWTH Aachen University, Aachen, Germany.ORCID 0000-0002-8903-0593
Annika SpottkeDepartment of Parkinson, Sleep and Movement Disorders, Centre of Neurology, University Hospital Bonn and German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.ORCID 0000-0001-9854-2972
Alexander StorchDepartment of Neurology, University of Rostock, Rostock, Germany.ORCID 0000-0002-1133-9216
Claudia TrenkwalderParacelsus-Elena Clinic, Centre of Parkinsonism and Movement Disorders, Kassel, Germany.ORCID 0000-0001-6407-1199
Jan KassubekDepartment of Neurology, University Hospital Ulm, Ulm, Germany.ORCID 0000-0002-7106-9270
Karsten WittDepartment of Neurology, School of Medicine and Health Sciences, Carl von Ossietzky University of Oldenburg, Oldenburg, Germany.
Richard DodelDepartment of Geriatric Medicine and Center for Translational and Behavioral Neuroscience, University Duisburg-Essen, Essen, Germany.ORCID 0000-0003-2044-6299
Ullrich WüllnerDepartment of Parkinson, Sleep and Movement Disorders, Centre of Neurology, University Hospital Bonn and German Center for Neurodegenerative Diseases (DZNE), Bonn, Germany.ORCID 0000-0002-3132-0790
Alfredo RamirezDivision of Neurogenetics and Molecular Psychiatry, Department of Psychiatry and Psychotherapy, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.ORCID 0000-0003-4991-763X
Maria Carolina DalmassoDivision of Neurogenetics and Molecular Psychiatry, Department of Psychiatry and Psychotherapy, Faculty of Medicine and University Hospital Cologne, University of Cologne, Cologne, Germany.ORCID 0000-0002-4901-9955

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

Parkinson's disease (PD) is marked by motor symptoms and often accompanied by mild cognitive impairment (PD-MCI), affecting up to 50% of patients and preceding PD dementia (PDD). Genetic factors may influence this progression, yet the underlying mechanisms remain unclear. This study investigated genetic factors influencing the progression from PD-MCI to PDD using polygenic risk scores (PRS). A genome-wide association study (GWAS) was conducted using data from the LANDSCAPE study. Multivariable Cox regression, Kaplan-Meier survival analysis, and concordance statistics assessed the relationship between PRS and PDD progression. No significant association was found between PD PRS and the risk of developing PDD.

Indexed as

Alzheimer DiseaseCognitive DysfunctionDementiaDisease ProgressionParkinson DiseaseAgedFemaleGenetic Predisposition to DiseaseGenome-Wide Association StudyHumansMaleMiddle AgedMultifactorial InheritanceAlzheimer's diseasegenome-wide association studymild cognitive impairmentParkinson's diseasesingle nucleotide polymorphism

Identifiers

PMID40739885
PMCPMC13347514

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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.