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dc.creatorMaraki M.I., Hatzimanolis A., Mourtzi N., Stefanis L., Yannakoulia M., Kosmidis M.H., Dardiotis E., Hadjigeorgiou G.M., Sakka P., Ramirez A., Grenier-Boley B., Lambert J.-C., Heilmann-Heimbach S., Stamelou M., Scarmeas N., Xiromerisiou G.en
dc.date.accessioned2023-01-31T08:57:14Z
dc.date.available2023-01-31T08:57:14Z
dc.date.issued2021
dc.identifier10.3389/fnmol.2021.739571
dc.identifier.issn16625099
dc.identifier.urihttp://hdl.handle.net/11615/76333
dc.description.abstractSeveral studies have investigated the association of the Parkinson’s disease (PD) polygenic risk score (PRS) with several aspects of well-established PD. We sought to evaluate the association of PRS with the prodromal stage of PD. We calculated PRS in a longitudinal sample (n = 1120) of community dwelling individuals ≥ 65 years from the HELIAD (The Hellenic Longitudinal Investigation of Aging and Diet) study in order to evaluate the association of this score with the probability of prodromal PD or any of the established risk and prodromal markers in MDS research criteria, using regression multi-adjusted models. Increases in PRS estimated from GWAS summary statistics’ ninety top SNPS with p < 5 × 10–8 was associated with increased odds of having probable/possible prodromal PD (i.e., ≥ 30% probability, OR = 1.033, 95%CI: 1.009–1.057 p = 0.006). From the prodromal PD risk markers, significant association was found between PRS and global cognitive deficit exclusively (p = 0.003). To our knowledge, our study is the first population based study investigating the association between PRS scores and prodromal markers of Parkinson’s disease. Our results suggest a strong relationship between the accumulation of many common genetic variants, as measured by PRS, and cognitive deficits. Copyright © 2021 Maraki, Hatzimanolis, Mourtzi, Stefanis, Yannakoulia, Kosmidis, Dardiotis, Hadjigeorgiou, Sakka, Ramirez, Grenier-Boley, Lambert, Heilmann-Heimbach, Stamelou, Scarmeas and Xiromerisiou.en
dc.language.isoenen
dc.sourceFrontiers in Molecular Neuroscienceen
dc.source.urihttps://www.scopus.com/inward/record.uri?eid=2-s2.0-85122193234&doi=10.3389%2ffnmol.2021.739571&partnerID=40&md5=6a36176e66b350a4411e2cec5f2f23e4
dc.subjectageden
dc.subjectanxietyen
dc.subjectArticleen
dc.subjectcommunity dwelling personen
dc.subjectcomputer assisted tomographyen
dc.subjectconstipationen
dc.subjectdementiaen
dc.subjectdepressionen
dc.subjectfemaleen
dc.subjectfood frequency questionnaireen
dc.subjectgene frequencyen
dc.subjectgenetic associationen
dc.subjectgenetic risk scoreen
dc.subjectgenetic variabilityen
dc.subjectgenome-wide association studyen
dc.subjectgenotypeen
dc.subjecthaplotypeen
dc.subjectheterozygosityen
dc.subjecthumanen
dc.subjecthypotensionen
dc.subjectmajor clinical studyen
dc.subjectmaleen
dc.subjectmild cognitive impairmenten
dc.subjectneuropsychological testen
dc.subjectorthostatic hypotensionen
dc.subjectParkinson diseaseen
dc.subjectparkinsonismen
dc.subjectprincipal component analysisen
dc.subjectquality controlen
dc.subjectREM sleepen
dc.subjectsingle nucleotide polymorphismen
dc.subjectstructured questionnaireen
dc.subjectUnified Parkinson Disease Rating Scaleen
dc.subjectFrontiers Media S.A.en
dc.titleAssociation of the Polygenic Risk Score With the Probability of Prodromal Parkinson’s Disease in Older Adultsen
dc.typejournalArticleen


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