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Screening for Mild Cognitive Impairment in Parkinson's Disease: Comparison of the Italian Versions of Three Neuropsychological Tests

Mild cognitive impairment (MCI) is frequent in Parkinson's disease (PD). Recently proposed criteria for MCI in PD (PD-MCI) indicate level I diagnosis based on abbreviated assessment and level II based on comprehensive neuropsychological evaluation. The study explored the sensitivity and specifi...

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Autores principales: Federico, Angela, Maier, Alice, Vianello, Greta, Mapelli, Daniela, Trentin, Michela, Zanette, Giampietro, Picelli, Alessandro, Gandolfi, Marialuisa, Tamburin, Stefano
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Hindawi Publishing Corporation 2015
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655066/
https://www.ncbi.nlm.nih.gov/pubmed/26634171
http://dx.doi.org/10.1155/2015/681976
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author Federico, Angela
Maier, Alice
Vianello, Greta
Mapelli, Daniela
Trentin, Michela
Zanette, Giampietro
Picelli, Alessandro
Gandolfi, Marialuisa
Tamburin, Stefano
author_facet Federico, Angela
Maier, Alice
Vianello, Greta
Mapelli, Daniela
Trentin, Michela
Zanette, Giampietro
Picelli, Alessandro
Gandolfi, Marialuisa
Tamburin, Stefano
author_sort Federico, Angela
collection PubMed
description Mild cognitive impairment (MCI) is frequent in Parkinson's disease (PD). Recently proposed criteria for MCI in PD (PD-MCI) indicate level I diagnosis based on abbreviated assessment and level II based on comprehensive neuropsychological evaluation. The study explored the sensitivity and specificity of the Italian versions of three neuropsychological tests for level I diagnosis of PD-MCI. We recruited 100 consecutive PD patients. After screening for inclusion criteria, 43 patients were included. The sensitivity and specificity of the Mini Mental State Examination (MMSE), the Montreal Cognitive Assessment (MoCA), and the Addenbrooke's Cognitive Examination Revised (ACE-R) in comparison to level II diagnosis of PD-MCI were examined. PD-MCI was diagnosed (level II) in 51% of patients. Disease duration was significantly longer and PD motor scales were more severely impaired in MCI group. The receiver-operator characteristics curve documented nonsignificant difference in the performance of the three tests, with slight advantage of MMSE (corrected data). The time of administration favored MMSE. In Italian-speaking PD patients, MMSE might represent a good screening tool for PD-MCI, because of the shorter time of administration and the performance comparable to those of MoCA and ACE-R. Further studies are needed to validate the new PD-MCI criteria across different languages and cultures.
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spelling pubmed-46550662015-12-02 Screening for Mild Cognitive Impairment in Parkinson's Disease: Comparison of the Italian Versions of Three Neuropsychological Tests Federico, Angela Maier, Alice Vianello, Greta Mapelli, Daniela Trentin, Michela Zanette, Giampietro Picelli, Alessandro Gandolfi, Marialuisa Tamburin, Stefano Parkinsons Dis Research Article Mild cognitive impairment (MCI) is frequent in Parkinson's disease (PD). Recently proposed criteria for MCI in PD (PD-MCI) indicate level I diagnosis based on abbreviated assessment and level II based on comprehensive neuropsychological evaluation. The study explored the sensitivity and specificity of the Italian versions of three neuropsychological tests for level I diagnosis of PD-MCI. We recruited 100 consecutive PD patients. After screening for inclusion criteria, 43 patients were included. The sensitivity and specificity of the Mini Mental State Examination (MMSE), the Montreal Cognitive Assessment (MoCA), and the Addenbrooke's Cognitive Examination Revised (ACE-R) in comparison to level II diagnosis of PD-MCI were examined. PD-MCI was diagnosed (level II) in 51% of patients. Disease duration was significantly longer and PD motor scales were more severely impaired in MCI group. The receiver-operator characteristics curve documented nonsignificant difference in the performance of the three tests, with slight advantage of MMSE (corrected data). The time of administration favored MMSE. In Italian-speaking PD patients, MMSE might represent a good screening tool for PD-MCI, because of the shorter time of administration and the performance comparable to those of MoCA and ACE-R. Further studies are needed to validate the new PD-MCI criteria across different languages and cultures. Hindawi Publishing Corporation 2015 2015-11-08 /pmc/articles/PMC4655066/ /pubmed/26634171 http://dx.doi.org/10.1155/2015/681976 Text en Copyright © 2015 Angela Federico et al. https://creativecommons.org/licenses/by/3.0/ This is an open access article distributed under the Creative Commons Attribution License, which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Research Article
Federico, Angela
Maier, Alice
Vianello, Greta
Mapelli, Daniela
Trentin, Michela
Zanette, Giampietro
Picelli, Alessandro
Gandolfi, Marialuisa
Tamburin, Stefano
Screening for Mild Cognitive Impairment in Parkinson's Disease: Comparison of the Italian Versions of Three Neuropsychological Tests
title Screening for Mild Cognitive Impairment in Parkinson's Disease: Comparison of the Italian Versions of Three Neuropsychological Tests
title_full Screening for Mild Cognitive Impairment in Parkinson's Disease: Comparison of the Italian Versions of Three Neuropsychological Tests
title_fullStr Screening for Mild Cognitive Impairment in Parkinson's Disease: Comparison of the Italian Versions of Three Neuropsychological Tests
title_full_unstemmed Screening for Mild Cognitive Impairment in Parkinson's Disease: Comparison of the Italian Versions of Three Neuropsychological Tests
title_short Screening for Mild Cognitive Impairment in Parkinson's Disease: Comparison of the Italian Versions of Three Neuropsychological Tests
title_sort screening for mild cognitive impairment in parkinson's disease: comparison of the italian versions of three neuropsychological tests
topic Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4655066/
https://www.ncbi.nlm.nih.gov/pubmed/26634171
http://dx.doi.org/10.1155/2015/681976
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