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Evaluating Mild Cognitive Dysfunction in Patients with Parkinson’s Disease in Clinical Practice in Taiwan
Our study aimed to examine the contribution of commonly used tools, including the Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA), and develop a formula for conversion of these tests in the Chinese population. We also create a predictive model for the detection of Chine...
Autores principales: | , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978523/ https://www.ncbi.nlm.nih.gov/pubmed/31974411 http://dx.doi.org/10.1038/s41598-020-58042-2 |
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author | Yu, Rwei-Ling Lee, Wei-Ju Li, Jie-Yuan Chang, Yung-Yee Chen, Chin-Chung Lin, Juei-Jueng Sung, Yueh-Feng Lin, Tsu-Kung Fuh, Jong-Ling |
author_facet | Yu, Rwei-Ling Lee, Wei-Ju Li, Jie-Yuan Chang, Yung-Yee Chen, Chin-Chung Lin, Juei-Jueng Sung, Yueh-Feng Lin, Tsu-Kung Fuh, Jong-Ling |
author_sort | Yu, Rwei-Ling |
collection | PubMed |
description | Our study aimed to examine the contribution of commonly used tools, including the Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA), and develop a formula for conversion of these tests in the Chinese population. We also create a predictive model for the detection of Chinese patients’ mild cognitive impairment (MCI). We recruited 168 patients with Parkinson’s disease (PD) from 12 medical centres or teaching hospitals in Taiwan, and each participant received a comprehensive neuropsychological assessment. Logistic regression analysis was conducted to find predictors of MCI with the help of a generalized additive model. We found that patients with an MMSE > 25 or a MoCA > 21 were less likely to have MCI. The discrimination powers of the two tests used for detecting MCI were 0.902 and 0.868, respectively, as measured by the area under the receiver operating characteristic curve (ROC). The best predictive model suggested that patients with a higher MMSE score, delayed recall scores of the 12-item Word Recall Test ≥ 5.817, and no test decline in the visuospatial index were less likely to have MCI (ROC = 0.982). Our findings have clinical utility in MCI detection in Chinese PD and need a larger sample to confirm. |
format | Online Article Text |
id | pubmed-6978523 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-69785232020-01-30 Evaluating Mild Cognitive Dysfunction in Patients with Parkinson’s Disease in Clinical Practice in Taiwan Yu, Rwei-Ling Lee, Wei-Ju Li, Jie-Yuan Chang, Yung-Yee Chen, Chin-Chung Lin, Juei-Jueng Sung, Yueh-Feng Lin, Tsu-Kung Fuh, Jong-Ling Sci Rep Article Our study aimed to examine the contribution of commonly used tools, including the Mini-Mental State Examination (MMSE) and Montreal Cognitive Assessment (MoCA), and develop a formula for conversion of these tests in the Chinese population. We also create a predictive model for the detection of Chinese patients’ mild cognitive impairment (MCI). We recruited 168 patients with Parkinson’s disease (PD) from 12 medical centres or teaching hospitals in Taiwan, and each participant received a comprehensive neuropsychological assessment. Logistic regression analysis was conducted to find predictors of MCI with the help of a generalized additive model. We found that patients with an MMSE > 25 or a MoCA > 21 were less likely to have MCI. The discrimination powers of the two tests used for detecting MCI were 0.902 and 0.868, respectively, as measured by the area under the receiver operating characteristic curve (ROC). The best predictive model suggested that patients with a higher MMSE score, delayed recall scores of the 12-item Word Recall Test ≥ 5.817, and no test decline in the visuospatial index were less likely to have MCI (ROC = 0.982). Our findings have clinical utility in MCI detection in Chinese PD and need a larger sample to confirm. Nature Publishing Group UK 2020-01-23 /pmc/articles/PMC6978523/ /pubmed/31974411 http://dx.doi.org/10.1038/s41598-020-58042-2 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Yu, Rwei-Ling Lee, Wei-Ju Li, Jie-Yuan Chang, Yung-Yee Chen, Chin-Chung Lin, Juei-Jueng Sung, Yueh-Feng Lin, Tsu-Kung Fuh, Jong-Ling Evaluating Mild Cognitive Dysfunction in Patients with Parkinson’s Disease in Clinical Practice in Taiwan |
title | Evaluating Mild Cognitive Dysfunction in Patients with Parkinson’s Disease in Clinical Practice in Taiwan |
title_full | Evaluating Mild Cognitive Dysfunction in Patients with Parkinson’s Disease in Clinical Practice in Taiwan |
title_fullStr | Evaluating Mild Cognitive Dysfunction in Patients with Parkinson’s Disease in Clinical Practice in Taiwan |
title_full_unstemmed | Evaluating Mild Cognitive Dysfunction in Patients with Parkinson’s Disease in Clinical Practice in Taiwan |
title_short | Evaluating Mild Cognitive Dysfunction in Patients with Parkinson’s Disease in Clinical Practice in Taiwan |
title_sort | evaluating mild cognitive dysfunction in patients with parkinson’s disease in clinical practice in taiwan |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6978523/ https://www.ncbi.nlm.nih.gov/pubmed/31974411 http://dx.doi.org/10.1038/s41598-020-58042-2 |
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