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Cognitive processes of apathy in Huntington’s disease show high sensitivity to disease progression
BACKGROUND: Disease-modifying treatments for Huntington’s disease (HD) are entering clinical trials: there is a pressing need for objective outcome measures of disease progression. Our previous work showed an association between 2 novel, objective cognitive tasks and apathy - a core feature of disea...
Autores principales: | , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Elsevier
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673112/ https://www.ncbi.nlm.nih.gov/pubmed/36405870 http://dx.doi.org/10.1016/j.prdoa.2022.100168 |
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author | Hare, Emily Bachoud-Lévi, Anne-Catherine Reilmann, Ralf Craufurd, David Busse, Monica Rosser, Anne McLauchlan, Duncan |
author_facet | Hare, Emily Bachoud-Lévi, Anne-Catherine Reilmann, Ralf Craufurd, David Busse, Monica Rosser, Anne McLauchlan, Duncan |
author_sort | Hare, Emily |
collection | PubMed |
description | BACKGROUND: Disease-modifying treatments for Huntington’s disease (HD) are entering clinical trials: there is a pressing need for objective outcome measures of disease progression. Our previous work showed an association between 2 novel, objective cognitive tasks and apathy - a core feature of disease progression in HD. OBJECTIVE: Evaluate the longitudinal validity and sensitivity of the novel Persistence and Maze tasks to assess their utility as clinical outcome measures in HD. METHODS: 83 participants positive for the HD gene and 54 controls performed a battery of established and novel tools, at baseline and 12 month follow up. RESULTS: The Maze task was found to be the most sensitive measure of change at 12 months, including the current gold-standard measure (the composite disease progression score). CONCLUSION: The Maze task has potential as a novel outcome measure of disease progression in HD and may have utility in other major neurodegenerative diseases. |
format | Online Article Text |
id | pubmed-9673112 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Elsevier |
record_format | MEDLINE/PubMed |
spelling | pubmed-96731122022-11-19 Cognitive processes of apathy in Huntington’s disease show high sensitivity to disease progression Hare, Emily Bachoud-Lévi, Anne-Catherine Reilmann, Ralf Craufurd, David Busse, Monica Rosser, Anne McLauchlan, Duncan Clin Park Relat Disord Short Communications BACKGROUND: Disease-modifying treatments for Huntington’s disease (HD) are entering clinical trials: there is a pressing need for objective outcome measures of disease progression. Our previous work showed an association between 2 novel, objective cognitive tasks and apathy - a core feature of disease progression in HD. OBJECTIVE: Evaluate the longitudinal validity and sensitivity of the novel Persistence and Maze tasks to assess their utility as clinical outcome measures in HD. METHODS: 83 participants positive for the HD gene and 54 controls performed a battery of established and novel tools, at baseline and 12 month follow up. RESULTS: The Maze task was found to be the most sensitive measure of change at 12 months, including the current gold-standard measure (the composite disease progression score). CONCLUSION: The Maze task has potential as a novel outcome measure of disease progression in HD and may have utility in other major neurodegenerative diseases. Elsevier 2022-10-26 /pmc/articles/PMC9673112/ /pubmed/36405870 http://dx.doi.org/10.1016/j.prdoa.2022.100168 Text en © 2022 Published by Elsevier Ltd. https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/). |
spellingShingle | Short Communications Hare, Emily Bachoud-Lévi, Anne-Catherine Reilmann, Ralf Craufurd, David Busse, Monica Rosser, Anne McLauchlan, Duncan Cognitive processes of apathy in Huntington’s disease show high sensitivity to disease progression |
title | Cognitive processes of apathy in Huntington’s disease show high sensitivity to disease progression |
title_full | Cognitive processes of apathy in Huntington’s disease show high sensitivity to disease progression |
title_fullStr | Cognitive processes of apathy in Huntington’s disease show high sensitivity to disease progression |
title_full_unstemmed | Cognitive processes of apathy in Huntington’s disease show high sensitivity to disease progression |
title_short | Cognitive processes of apathy in Huntington’s disease show high sensitivity to disease progression |
title_sort | cognitive processes of apathy in huntington’s disease show high sensitivity to disease progression |
topic | Short Communications |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9673112/ https://www.ncbi.nlm.nih.gov/pubmed/36405870 http://dx.doi.org/10.1016/j.prdoa.2022.100168 |
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