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Visuospatial dysfunction indicates an increased risk of rapid dementia conversion in Parkinson's disease

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dc.contributor.authorPark, Chan Wook-
dc.contributor.authorChoi, Youngseok-
dc.contributor.authorSun, Yeeun-
dc.contributor.authorLee, Hye Sun-
dc.contributor.authorLee, Phil Hyu-
dc.contributor.authorKim, Yun Joong-
dc.contributor.authorSohn, Young H.-
dc.contributor.authorLee, Jeyeon-
dc.contributor.authorChung, Seok Jong-
dc.date.accessioned2026-03-24T05:00:24Z-
dc.date.available2026-03-24T05:00:24Z-
dc.date.issued2026-01-
dc.identifier.issn1552-5260-
dc.identifier.issn1552-5279-
dc.identifier.urihttps://scholarworks.bwise.kr/hanyang/handle/2021.sw.hanyang/211517-
dc.description.abstractINTRODUCTION The aim of this study was to define cognitive subtypes of early-stage Parkinson's disease (PD) based on temporal evolutionary patterns of domain-specific decline. METHODS We retrospectively enrolled 474 patients with early-stage PD who underwent detailed neuropsychological testing at initial assessment. Age- and education-specific z-scores from 13 neuropsychological subtests were used to apply Subtype and Stage Inference (SuStaIn) to identify distinct cognitive subtypes. We compared the risk of developing dementia between subtypes. RESULTS SuStaIn analysis delineated three pd subtypes with cognitive impairment: Subtype 1 (n = 121) with early verbal memory impairment; Subtype 2 (n = 108) with early visuospatial dysfunction; and Subtype 3 (n = 87) with early frontal/executive dysfunction. The remaining 158 patients were classified as a cognitively intact subtype (Subtype 0). Time-dependent Cox regression models showed that the risk of dementia after 3.5 years was highest in Subtype 2. DISCUSSION Visuospatial dysfunction may be a potential cognitive profile for predicting the risk of rapid dementia conversion in PD.-
dc.format.extent14-
dc.language영어-
dc.language.isoENG-
dc.publisherWILEY-
dc.titleVisuospatial dysfunction indicates an increased risk of rapid dementia conversion in Parkinson's disease-
dc.typeArticle-
dc.publisher.location미국-
dc.identifier.doi10.1002/alz.71130-
dc.identifier.scopusid2-s2.0-105027703352-
dc.identifier.wosid001663710400001-
dc.identifier.bibliographicCitationALZHEIMERS & DEMENTIA, v.22, no.1, pp 1 - 14-
dc.citation.titleALZHEIMERS & DEMENTIA-
dc.citation.volume22-
dc.citation.number1-
dc.citation.startPage1-
dc.citation.endPage14-
dc.type.docTypeArticle-
dc.description.isOpenAccessY-
dc.description.journalRegisteredClassscie-
dc.description.journalRegisteredClassscopus-
dc.relation.journalResearchAreaNeurosciences & Neurology-
dc.relation.journalWebOfScienceCategoryClinical Neurology-
dc.subject.keywordPlusMILD COGNITIVE IMPAIRMENT-
dc.subject.keywordPlusCLINICAL DIAGNOSTIC-CRITERIA-
dc.subject.keywordPlusMEMORY-
dc.subject.keywordPlusCAMPAIGN-
dc.subject.keywordPlusDECLINE-
dc.subject.keywordAuthorcognitive profile-
dc.subject.keywordAuthordementia-
dc.subject.keywordAuthorSubtype and Stage Inference (SuStaIn)-
dc.subject.keywordAuthorParkinson’s disease-
dc.subject.keywordAuthorvisuospatial-
dc.identifier.urlhttps://alz-journals.onlinelibrary.wiley.com/doi/10.1002/alz.71130-
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