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@ARTICLE{Parveen:281870,
author = {Parveen, Kayenat and Ross, J Alexander and van der Wurp,
Hendrik and Balzer-Geldsetzer, Monika and Berg, Daniela and
Deuschl, Günther and Gasser, Thomas and Hilker-Roggendorf,
Rüdiger and Kalbe, Elke and Liepelt-Scarfone, Inga and
Mollenhauer, Brit and Riedel, Oliver and Röske, Sandra and
Schulz, Jörg B and Spottke, Annika and Storch, Alexander
and Trenkwalder, Claudia and Kassubek, Jan and Witt, Karsten
and Dodel, Richard and Wüllner, Ullrich and Ramirez,
Alfredo and Dalmasso, Maria Carolina},
title = {{P}rogression to {P}arkinson's dementia is not modulated by
genetic risk variants for {A}lzheimer's or {P}arkinson's
disease.},
journal = {Journal of Parkinson's Disease},
volume = {15},
number = {7},
issn = {1877-7171},
address = {Amsterdam},
publisher = {IOS Press},
reportid = {DZNE-2025-01241},
pages = {1304 - 1311},
year = {2025},
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.},
keywords = {Humans / Parkinson Disease: genetics / Parkinson Disease:
complications / Genome-Wide Association Study / Male / Aged
/ Female / Disease Progression / Cognitive Dysfunction:
genetics / Cognitive Dysfunction: etiology / Alzheimer
Disease: genetics / Dementia: genetics / Dementia: etiology
/ Middle Aged / Genetic Predisposition to Disease /
Multifactorial Inheritance / Alzheimer's disease (Other) /
Parkinson's disease (Other) / genome-wide association study
(Other) / mild cognitive impairment (Other) / single
nucleotide polymorphism (Other)},
cin = {AG Gasser / AG Wagner / AG Spottke / Clinical Research
Platform (CRP) / AG Storch / Clinical Study Center (Ulm) /
AG Wüllner / Patient Studies (Bonn)},
ddc = {610},
cid = {I:(DE-2719)1210000 / I:(DE-2719)1011201 /
I:(DE-2719)1011103 / I:(DE-2719)1011401 / I:(DE-2719)5000014
/ I:(DE-2719)5000077 / I:(DE-2719)1011302 /
I:(DE-2719)1011101},
pnm = {353 - Clinical and Health Care Research (POF4-353)},
pid = {G:(DE-HGF)POF4-353},
typ = {PUB:(DE-HGF)16},
pubmed = {pmid:40739885},
doi = {10.1177/1877718X251356512},
url = {https://pub.dzne.de/record/281870},
}