Cargando…

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...

Descripción completa

Detalles Bibliográficos
Autores principales: Hare, Emily, Bachoud-Lévi, Anne-Catherine, Reilmann, Ralf, Craufurd, David, Busse, Monica, Rosser, Anne, McLauchlan, Duncan
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Elsevier 2022
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
_version_ 1784832881173987328
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
work_keys_str_mv AT hareemily cognitiveprocessesofapathyinhuntingtonsdiseaseshowhighsensitivitytodiseaseprogression
AT bachoudleviannecatherine cognitiveprocessesofapathyinhuntingtonsdiseaseshowhighsensitivitytodiseaseprogression
AT reilmannralf cognitiveprocessesofapathyinhuntingtonsdiseaseshowhighsensitivitytodiseaseprogression
AT craufurddavid cognitiveprocessesofapathyinhuntingtonsdiseaseshowhighsensitivitytodiseaseprogression
AT bussemonica cognitiveprocessesofapathyinhuntingtonsdiseaseshowhighsensitivitytodiseaseprogression
AT rosseranne cognitiveprocessesofapathyinhuntingtonsdiseaseshowhighsensitivitytodiseaseprogression
AT mclauchlanduncan cognitiveprocessesofapathyinhuntingtonsdiseaseshowhighsensitivitytodiseaseprogression