Factor analysis–derived cognitive profile predicting early dementia conversion in PD

OBJECTIVESTo investigate which baseline neuropsychological profile predicts the risk of developing dementia in early-stage Parkinson disease (PD). METHODSWe retrospectively reviewed detailed medical records of 350 drug-naive patients with early-stage PD (follow-up >3 years) who underwent a detail...

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Veröffentlicht in:Neurology 2020-09, Vol.95 (12), p.e1650-e1659
Hauptverfasser: Chung, Seok Jong, Lee, Hye Sun, Kim, Hang-Rai, Yoo, Han Soo, Lee, Yang Hyun, Jung, Jin Ho, Baik, KyoungWon, Ye, Byoung Seok, Sohn, Young H., Lee, Phil Hyu
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container_end_page e1659
container_issue 12
container_start_page e1650
container_title Neurology
container_volume 95
creator Chung, Seok Jong
Lee, Hye Sun
Kim, Hang-Rai
Yoo, Han Soo
Lee, Yang Hyun
Jung, Jin Ho
Baik, KyoungWon
Ye, Byoung Seok
Sohn, Young H.
Lee, Phil Hyu
description OBJECTIVESTo investigate which baseline neuropsychological profile predicts the risk of developing dementia in early-stage Parkinson disease (PD). METHODSWe retrospectively reviewed detailed medical records of 350 drug-naive patients with early-stage PD (follow-up >3 years) who underwent a detailed neuropsychological test at initial assessment. Factor analysis was conducted to determine cognitive profiles that yielded 4 cognitive function factorsfactor 1, visual memory/visuospatial; factor 2, verbal memory; factor 3, frontal/executive; and factor 4, attention/working memory/language. Subsequently, we assessed the effect of these cognitive function factors on the risk for dementia conversion. We also constructed a nomogram to calculate the risk for developing dementia over a 5-year follow-up period based on these cognitive profiles. RESULTSCox regression analysis demonstrated that a higher composite score of factor 1 (hazard ratio [HR] 0.558, 95% confidence interval [CI] 0.427–0.730), factor 2 (HR 0.768, 95% CI 0.596–0.991), and factor 3 (HR 0.425, 95% CI 0.305–0.593) was associated with a lower risk for dementia conversion, while factor 3 had the most predictive power. The nomogram had a fair ability (Heagerty integrated area under the curve 0.763) to estimate the risk for dementia conversion within 5 years. The composite scores of factor 3 contributed more to the occurrence of dementia in PD than those of the other cognitive function factors. CONCLUSIONSThese findings suggest that these factor analysis–derived cognitive profiles can be used to predict dementia conversion in early-stage PD. In addition, frontal/executive dysfunction contributes most to the occurrence of dementia in PD.
doi_str_mv 10.1212/WNL.0000000000010347
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METHODSWe retrospectively reviewed detailed medical records of 350 drug-naive patients with early-stage PD (follow-up &gt;3 years) who underwent a detailed neuropsychological test at initial assessment. Factor analysis was conducted to determine cognitive profiles that yielded 4 cognitive function factorsfactor 1, visual memory/visuospatial; factor 2, verbal memory; factor 3, frontal/executive; and factor 4, attention/working memory/language. Subsequently, we assessed the effect of these cognitive function factors on the risk for dementia conversion. We also constructed a nomogram to calculate the risk for developing dementia over a 5-year follow-up period based on these cognitive profiles. RESULTSCox regression analysis demonstrated that a higher composite score of factor 1 (hazard ratio [HR] 0.558, 95% confidence interval [CI] 0.427–0.730), factor 2 (HR 0.768, 95% CI 0.596–0.991), and factor 3 (HR 0.425, 95% CI 0.305–0.593) was associated with a lower risk for dementia conversion, while factor 3 had the most predictive power. The nomogram had a fair ability (Heagerty integrated area under the curve 0.763) to estimate the risk for dementia conversion within 5 years. The composite scores of factor 3 contributed more to the occurrence of dementia in PD than those of the other cognitive function factors. CONCLUSIONSThese findings suggest that these factor analysis–derived cognitive profiles can be used to predict dementia conversion in early-stage PD. In addition, frontal/executive dysfunction contributes most to the occurrence of dementia in PD.</description><identifier>ISSN: 0028-3878</identifier><identifier>EISSN: 1526-632X</identifier><identifier>DOI: 10.1212/WNL.0000000000010347</identifier><language>eng</language><publisher>American Academy of Neurology</publisher><ispartof>Neurology, 2020-09, Vol.95 (12), p.e1650-e1659</ispartof><rights>American Academy of Neurology</rights><rights>2020 American Academy of Neurology</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c3787-331ac9a16d496b3b14d64db2b67f8bd3e2842301253897c26bebee484342c5d63</citedby><cites>FETCH-LOGICAL-c3787-331ac9a16d496b3b14d64db2b67f8bd3e2842301253897c26bebee484342c5d63</cites><orcidid>0000-0003-0187-8440 ; 0000-0001-7215-375X</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27903,27904</link.rule.ids></links><search><creatorcontrib>Chung, Seok Jong</creatorcontrib><creatorcontrib>Lee, Hye Sun</creatorcontrib><creatorcontrib>Kim, Hang-Rai</creatorcontrib><creatorcontrib>Yoo, Han Soo</creatorcontrib><creatorcontrib>Lee, Yang Hyun</creatorcontrib><creatorcontrib>Jung, Jin Ho</creatorcontrib><creatorcontrib>Baik, KyoungWon</creatorcontrib><creatorcontrib>Ye, Byoung Seok</creatorcontrib><creatorcontrib>Sohn, Young H.</creatorcontrib><creatorcontrib>Lee, Phil Hyu</creatorcontrib><title>Factor analysis–derived cognitive profile predicting early dementia conversion in PD</title><title>Neurology</title><description>OBJECTIVESTo investigate which baseline neuropsychological profile predicts the risk of developing dementia in early-stage Parkinson disease (PD). METHODSWe retrospectively reviewed detailed medical records of 350 drug-naive patients with early-stage PD (follow-up &gt;3 years) who underwent a detailed neuropsychological test at initial assessment. Factor analysis was conducted to determine cognitive profiles that yielded 4 cognitive function factorsfactor 1, visual memory/visuospatial; factor 2, verbal memory; factor 3, frontal/executive; and factor 4, attention/working memory/language. Subsequently, we assessed the effect of these cognitive function factors on the risk for dementia conversion. We also constructed a nomogram to calculate the risk for developing dementia over a 5-year follow-up period based on these cognitive profiles. RESULTSCox regression analysis demonstrated that a higher composite score of factor 1 (hazard ratio [HR] 0.558, 95% confidence interval [CI] 0.427–0.730), factor 2 (HR 0.768, 95% CI 0.596–0.991), and factor 3 (HR 0.425, 95% CI 0.305–0.593) was associated with a lower risk for dementia conversion, while factor 3 had the most predictive power. The nomogram had a fair ability (Heagerty integrated area under the curve 0.763) to estimate the risk for dementia conversion within 5 years. The composite scores of factor 3 contributed more to the occurrence of dementia in PD than those of the other cognitive function factors. CONCLUSIONSThese findings suggest that these factor analysis–derived cognitive profiles can be used to predict dementia conversion in early-stage PD. 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METHODSWe retrospectively reviewed detailed medical records of 350 drug-naive patients with early-stage PD (follow-up &gt;3 years) who underwent a detailed neuropsychological test at initial assessment. Factor analysis was conducted to determine cognitive profiles that yielded 4 cognitive function factorsfactor 1, visual memory/visuospatial; factor 2, verbal memory; factor 3, frontal/executive; and factor 4, attention/working memory/language. Subsequently, we assessed the effect of these cognitive function factors on the risk for dementia conversion. We also constructed a nomogram to calculate the risk for developing dementia over a 5-year follow-up period based on these cognitive profiles. RESULTSCox regression analysis demonstrated that a higher composite score of factor 1 (hazard ratio [HR] 0.558, 95% confidence interval [CI] 0.427–0.730), factor 2 (HR 0.768, 95% CI 0.596–0.991), and factor 3 (HR 0.425, 95% CI 0.305–0.593) was associated with a lower risk for dementia conversion, while factor 3 had the most predictive power. The nomogram had a fair ability (Heagerty integrated area under the curve 0.763) to estimate the risk for dementia conversion within 5 years. The composite scores of factor 3 contributed more to the occurrence of dementia in PD than those of the other cognitive function factors. CONCLUSIONSThese findings suggest that these factor analysis–derived cognitive profiles can be used to predict dementia conversion in early-stage PD. 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title Factor analysis–derived cognitive profile predicting early dementia conversion in PD
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