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‘Two-level’ measurements of processing speed as cognitive markers in the differential diagnosis of DSM-5 mild neurocognitive disorders (NCD)
Processing speed is an updated diagnostic factor for neurocognitive disorders (NCD) in DSM-5. This study investigated the characteristics of processing speed and their diagnostic values in NCD patients. A flanker test was conducted in 31 adults with NCD due to vascular disease (NCD-vascular), 36 pat...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2017
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428878/ https://www.ncbi.nlm.nih.gov/pubmed/28364127 http://dx.doi.org/10.1038/s41598-017-00624-8 |
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author | Lu, Hanna Chan, Sandra S. M. Lam, Linda C. W. |
author_facet | Lu, Hanna Chan, Sandra S. M. Lam, Linda C. W. |
author_sort | Lu, Hanna |
collection | PubMed |
description | Processing speed is an updated diagnostic factor for neurocognitive disorders (NCD) in DSM-5. This study investigated the characteristics of processing speed and their diagnostic values in NCD patients. A flanker test was conducted in 31 adults with NCD due to vascular disease (NCD-vascular), 36 patients with NCD due to Alzheimer’s disease (NCD-AD), and 137 healthy controls. The processing speed was evaluated using two measurements: mean reaction time (RT) and intra-individual variability of RT. Mean RT represents the global processing speed. Intra-individual variability of RT is the short-term fluctuation of RT and consists of two indices, which are intra-individual coefficient of variation of reaction time (ICV-RT) and intra-individual standard deviations (iSD). We observed elevated ICV-RT and iSD in NCD-AD and NCD-vascular patients. Additionally, there was a slowed RT in NCD-AD patients. The intra-individual variability of RT had a moderate power to differentiate NCD subgroups. The mean RT was able to discriminate the NCD-AD from NCD-vascular patients. Our findings highlight the clinical utility of the combined ‘two-level’ measurements of processing speed to distinguish between individuals with different cognitive status. Furthermore, the ‘two-level’ features of processing speed embedded in the psychometric property may also reflect the diverse aetiology underlying certain ‘disease-specific’ neurocognitive disorders. |
format | Online Article Text |
id | pubmed-5428878 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2017 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-54288782017-05-15 ‘Two-level’ measurements of processing speed as cognitive markers in the differential diagnosis of DSM-5 mild neurocognitive disorders (NCD) Lu, Hanna Chan, Sandra S. M. Lam, Linda C. W. Sci Rep Article Processing speed is an updated diagnostic factor for neurocognitive disorders (NCD) in DSM-5. This study investigated the characteristics of processing speed and their diagnostic values in NCD patients. A flanker test was conducted in 31 adults with NCD due to vascular disease (NCD-vascular), 36 patients with NCD due to Alzheimer’s disease (NCD-AD), and 137 healthy controls. The processing speed was evaluated using two measurements: mean reaction time (RT) and intra-individual variability of RT. Mean RT represents the global processing speed. Intra-individual variability of RT is the short-term fluctuation of RT and consists of two indices, which are intra-individual coefficient of variation of reaction time (ICV-RT) and intra-individual standard deviations (iSD). We observed elevated ICV-RT and iSD in NCD-AD and NCD-vascular patients. Additionally, there was a slowed RT in NCD-AD patients. The intra-individual variability of RT had a moderate power to differentiate NCD subgroups. The mean RT was able to discriminate the NCD-AD from NCD-vascular patients. Our findings highlight the clinical utility of the combined ‘two-level’ measurements of processing speed to distinguish between individuals with different cognitive status. Furthermore, the ‘two-level’ features of processing speed embedded in the psychometric property may also reflect the diverse aetiology underlying certain ‘disease-specific’ neurocognitive disorders. Nature Publishing Group UK 2017-03-31 /pmc/articles/PMC5428878/ /pubmed/28364127 http://dx.doi.org/10.1038/s41598-017-00624-8 Text en © The Author(s) 2017 This work is licensed under a Creative Commons Attribution 4.0 International License. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in the credit line; if the material is not included under the Creative Commons license, users will need to obtain permission from the license holder to reproduce the material. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/ |
spellingShingle | Article Lu, Hanna Chan, Sandra S. M. Lam, Linda C. W. ‘Two-level’ measurements of processing speed as cognitive markers in the differential diagnosis of DSM-5 mild neurocognitive disorders (NCD) |
title | ‘Two-level’ measurements of processing speed as cognitive markers in the differential diagnosis of DSM-5 mild neurocognitive disorders (NCD) |
title_full | ‘Two-level’ measurements of processing speed as cognitive markers in the differential diagnosis of DSM-5 mild neurocognitive disorders (NCD) |
title_fullStr | ‘Two-level’ measurements of processing speed as cognitive markers in the differential diagnosis of DSM-5 mild neurocognitive disorders (NCD) |
title_full_unstemmed | ‘Two-level’ measurements of processing speed as cognitive markers in the differential diagnosis of DSM-5 mild neurocognitive disorders (NCD) |
title_short | ‘Two-level’ measurements of processing speed as cognitive markers in the differential diagnosis of DSM-5 mild neurocognitive disorders (NCD) |
title_sort | ‘two-level’ measurements of processing speed as cognitive markers in the differential diagnosis of dsm-5 mild neurocognitive disorders (ncd) |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5428878/ https://www.ncbi.nlm.nih.gov/pubmed/28364127 http://dx.doi.org/10.1038/s41598-017-00624-8 |
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