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Neural Substrates of Cognitive Subtypes in Parkinson's Disease: A 3-Year Longitudinal Study

BACKGROUND: The neuropsychological features and neuropathological progression patterns associated with rapidly evolving cognitive decline or dementia in Parkinson's disease (PD) remain to be elucidated. METHODS: Fifty-three PD patients without dementia were recruited to participate in a 3-year...

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Autores principales: Shoji, Yumiko, Nishio, Yoshiyuki, Baba, Toru, Uchiyama, Makoto, Yokoi, Kayoko, Ishioka, Toshiyuki, Hosokai, Yoshiyuki, Hirayama, Kazumi, Fukuda, Hiroshi, Aoki, Masashi, Hasegawa, Takafumi, Takeda, Atsushi, Mori, Etsuro
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Public Library of Science 2014
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203806/
https://www.ncbi.nlm.nih.gov/pubmed/25330390
http://dx.doi.org/10.1371/journal.pone.0110547
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author Shoji, Yumiko
Nishio, Yoshiyuki
Baba, Toru
Uchiyama, Makoto
Yokoi, Kayoko
Ishioka, Toshiyuki
Hosokai, Yoshiyuki
Hirayama, Kazumi
Fukuda, Hiroshi
Aoki, Masashi
Hasegawa, Takafumi
Takeda, Atsushi
Mori, Etsuro
author_facet Shoji, Yumiko
Nishio, Yoshiyuki
Baba, Toru
Uchiyama, Makoto
Yokoi, Kayoko
Ishioka, Toshiyuki
Hosokai, Yoshiyuki
Hirayama, Kazumi
Fukuda, Hiroshi
Aoki, Masashi
Hasegawa, Takafumi
Takeda, Atsushi
Mori, Etsuro
author_sort Shoji, Yumiko
collection PubMed
description BACKGROUND: The neuropsychological features and neuropathological progression patterns associated with rapidly evolving cognitive decline or dementia in Parkinson's disease (PD) remain to be elucidated. METHODS: Fifty-three PD patients without dementia were recruited to participate in a 3-year longitudinal cohort study. The patients were grouped according to the Clinical Dementia Rating (CDR). Group-wise comparisons were made with regard to demographic characteristics, motor symptoms, neuropsychological performances and 18F-fluorodeoxyglucose positron emission tomography. RESULTS: Patients who had memory-plus cognitive impairment (patients whose CDR was 0 at baseline and 0.5 in memory and other domains at follow-up, and those whose baseline CDR was 0.5 in memory and other domains) exhibited higher age at onset, visuoperceptual impairment, non-tremor-dominant motor disturbance, rapid symptomatic progression and posterior neocortical hypometabolism. In patients who were cognitively unimpaired and those who had memory-dominant cognitive impairment (patients whose CDR was 0 at baseline and 0.5 only in memory domain at follow-up, and those whose baseline CDR was 0.5 only in memory domain), the posterior neocortex was relatively unaffected until a later stage of the disease. CONCLUSIONS: These results suggest that visuoperceptual impairment and the early involvement of the posterior neocortex may be risk factors for rapid symptomatic progression and dementia in PD.
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spelling pubmed-42038062014-10-27 Neural Substrates of Cognitive Subtypes in Parkinson's Disease: A 3-Year Longitudinal Study Shoji, Yumiko Nishio, Yoshiyuki Baba, Toru Uchiyama, Makoto Yokoi, Kayoko Ishioka, Toshiyuki Hosokai, Yoshiyuki Hirayama, Kazumi Fukuda, Hiroshi Aoki, Masashi Hasegawa, Takafumi Takeda, Atsushi Mori, Etsuro PLoS One Research Article BACKGROUND: The neuropsychological features and neuropathological progression patterns associated with rapidly evolving cognitive decline or dementia in Parkinson's disease (PD) remain to be elucidated. METHODS: Fifty-three PD patients without dementia were recruited to participate in a 3-year longitudinal cohort study. The patients were grouped according to the Clinical Dementia Rating (CDR). Group-wise comparisons were made with regard to demographic characteristics, motor symptoms, neuropsychological performances and 18F-fluorodeoxyglucose positron emission tomography. RESULTS: Patients who had memory-plus cognitive impairment (patients whose CDR was 0 at baseline and 0.5 in memory and other domains at follow-up, and those whose baseline CDR was 0.5 in memory and other domains) exhibited higher age at onset, visuoperceptual impairment, non-tremor-dominant motor disturbance, rapid symptomatic progression and posterior neocortical hypometabolism. In patients who were cognitively unimpaired and those who had memory-dominant cognitive impairment (patients whose CDR was 0 at baseline and 0.5 only in memory domain at follow-up, and those whose baseline CDR was 0.5 only in memory domain), the posterior neocortex was relatively unaffected until a later stage of the disease. CONCLUSIONS: These results suggest that visuoperceptual impairment and the early involvement of the posterior neocortex may be risk factors for rapid symptomatic progression and dementia in PD. Public Library of Science 2014-10-20 /pmc/articles/PMC4203806/ /pubmed/25330390 http://dx.doi.org/10.1371/journal.pone.0110547 Text en © 2014 Shoji et al http://creativecommons.org/licenses/by/4.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original author and source are properly credited.
spellingShingle Research Article
Shoji, Yumiko
Nishio, Yoshiyuki
Baba, Toru
Uchiyama, Makoto
Yokoi, Kayoko
Ishioka, Toshiyuki
Hosokai, Yoshiyuki
Hirayama, Kazumi
Fukuda, Hiroshi
Aoki, Masashi
Hasegawa, Takafumi
Takeda, Atsushi
Mori, Etsuro
Neural Substrates of Cognitive Subtypes in Parkinson's Disease: A 3-Year Longitudinal Study
title Neural Substrates of Cognitive Subtypes in Parkinson's Disease: A 3-Year Longitudinal Study
title_full Neural Substrates of Cognitive Subtypes in Parkinson's Disease: A 3-Year Longitudinal Study
title_fullStr Neural Substrates of Cognitive Subtypes in Parkinson's Disease: A 3-Year Longitudinal Study
title_full_unstemmed Neural Substrates of Cognitive Subtypes in Parkinson's Disease: A 3-Year Longitudinal Study
title_short Neural Substrates of Cognitive Subtypes in Parkinson's Disease: A 3-Year Longitudinal Study
title_sort neural substrates of cognitive subtypes in parkinson's disease: a 3-year longitudinal study
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4203806/
https://www.ncbi.nlm.nih.gov/pubmed/25330390
http://dx.doi.org/10.1371/journal.pone.0110547
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