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Profile of cognitive impairment in late‐stage Parkinson's disease

INTRODUCTION: The profile of cognitive impairment associated with the late stages of Parkinson's disease (LSPD) is rarely reported. Its characterization is necessary to better understand the cognitive changes that occur as the disease progresses and to better contribute to its management. METHO...

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Autores principales: Severiano e Sousa, Catarina, Fabbri, Margherita, Godinho, Catarina, Moiron Simões, Rita, Chendo, Inês, Coelho, Miguel, Pavão Martins, Isabel, Ferreira, Joaquim J.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: John Wiley and Sons Inc. 2022
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014988/
https://www.ncbi.nlm.nih.gov/pubmed/35254007
http://dx.doi.org/10.1002/brb3.2537
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author Severiano e Sousa, Catarina
Fabbri, Margherita
Godinho, Catarina
Moiron Simões, Rita
Chendo, Inês
Coelho, Miguel
Pavão Martins, Isabel
Ferreira, Joaquim J.
author_facet Severiano e Sousa, Catarina
Fabbri, Margherita
Godinho, Catarina
Moiron Simões, Rita
Chendo, Inês
Coelho, Miguel
Pavão Martins, Isabel
Ferreira, Joaquim J.
author_sort Severiano e Sousa, Catarina
collection PubMed
description INTRODUCTION: The profile of cognitive impairment associated with the late stages of Parkinson's disease (LSPD) is rarely reported. Its characterization is necessary to better understand the cognitive changes that occur as the disease progresses and to better contribute to its management. METHODS: In this cross‐sectional study, we characterized the cognitive profile of LSPD patients using the comprehensive assessment methodology proposed by the International Parkinson and Movement Disorders Society Task Force. The association of clinical and demographic variables with dementia diagnosis was also investigated using binary logistic regression analysis. RESULTS: Eighty‐four LSPD patients were included (age 75.4 ± 6.9; disease duration 16.9 ± 7.5). Fifty‐four (64.3%) were classified as demented and presented a global impairment cognitive profile. In the nondemented group (N = 30), 25 (83.3%) LSPD patients met the diagnostic criteria for mild cognitive impairment, mostly with multiple domain impairment (96.0%) and a heterogeneous profile. Memory was the most frequent and severely impaired cognitive domain in both groups. Disease disability, orientation, complex order comprehension, verbal learning, and visuoconstructive abilities were significantly associated with dementia diagnosis (p < .05). CONCLUSIONS: Cognitive impairment in multiple domains was common in LSPD patients. The most frequent and prominent deficits were in the memory domain, with a strong interference from attention impairment. Disease disability, orientation, complex order comprehension, verbal learning, and visuoconstructive abilities proved to be important determinants for dementia diagnosis.
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spelling pubmed-90149882022-04-20 Profile of cognitive impairment in late‐stage Parkinson's disease Severiano e Sousa, Catarina Fabbri, Margherita Godinho, Catarina Moiron Simões, Rita Chendo, Inês Coelho, Miguel Pavão Martins, Isabel Ferreira, Joaquim J. Brain Behav Original Articles INTRODUCTION: The profile of cognitive impairment associated with the late stages of Parkinson's disease (LSPD) is rarely reported. Its characterization is necessary to better understand the cognitive changes that occur as the disease progresses and to better contribute to its management. METHODS: In this cross‐sectional study, we characterized the cognitive profile of LSPD patients using the comprehensive assessment methodology proposed by the International Parkinson and Movement Disorders Society Task Force. The association of clinical and demographic variables with dementia diagnosis was also investigated using binary logistic regression analysis. RESULTS: Eighty‐four LSPD patients were included (age 75.4 ± 6.9; disease duration 16.9 ± 7.5). Fifty‐four (64.3%) were classified as demented and presented a global impairment cognitive profile. In the nondemented group (N = 30), 25 (83.3%) LSPD patients met the diagnostic criteria for mild cognitive impairment, mostly with multiple domain impairment (96.0%) and a heterogeneous profile. Memory was the most frequent and severely impaired cognitive domain in both groups. Disease disability, orientation, complex order comprehension, verbal learning, and visuoconstructive abilities were significantly associated with dementia diagnosis (p < .05). CONCLUSIONS: Cognitive impairment in multiple domains was common in LSPD patients. The most frequent and prominent deficits were in the memory domain, with a strong interference from attention impairment. Disease disability, orientation, complex order comprehension, verbal learning, and visuoconstructive abilities proved to be important determinants for dementia diagnosis. John Wiley and Sons Inc. 2022-03-07 /pmc/articles/PMC9014988/ /pubmed/35254007 http://dx.doi.org/10.1002/brb3.2537 Text en © 2022 The Authors. Brain and Behavior published by Wiley Periodicals LLC https://creativecommons.org/licenses/by/4.0/This is an open access article under the terms of the http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) License, which permits use, distribution and reproduction in any medium, provided the original work is properly cited.
spellingShingle Original Articles
Severiano e Sousa, Catarina
Fabbri, Margherita
Godinho, Catarina
Moiron Simões, Rita
Chendo, Inês
Coelho, Miguel
Pavão Martins, Isabel
Ferreira, Joaquim J.
Profile of cognitive impairment in late‐stage Parkinson's disease
title Profile of cognitive impairment in late‐stage Parkinson's disease
title_full Profile of cognitive impairment in late‐stage Parkinson's disease
title_fullStr Profile of cognitive impairment in late‐stage Parkinson's disease
title_full_unstemmed Profile of cognitive impairment in late‐stage Parkinson's disease
title_short Profile of cognitive impairment in late‐stage Parkinson's disease
title_sort profile of cognitive impairment in late‐stage parkinson's disease
topic Original Articles
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9014988/
https://www.ncbi.nlm.nih.gov/pubmed/35254007
http://dx.doi.org/10.1002/brb3.2537
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