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Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease

BACKGROUND: Deterioration of cognitive functioning is a debilitating symptom in many neurodegenerative diseases, such as Huntington's disease (HD). To date, there are no effective treatments for the cognitive problems associated with HD. Cognitive assessment outcomes will have a central role in...

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Autores principales: Stout, Julie C, Jones, Rebecca, Labuschagne, Izelle, O'Regan, Alison M, Say, Miranda J, Dumas, Eve M, Queller, Sarah, Justo, Damian, Santos, Rachelle Dar, Coleman, Allison, Hart, Ellen P, Dürr, Alexandra, Leavitt, Blair R, Roos, Raymund A, Langbehn, Doug R, Tabrizi, Sarah J, Frost, Chris
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BMJ Group 2012
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368487/
https://www.ncbi.nlm.nih.gov/pubmed/22566599
http://dx.doi.org/10.1136/jnnp-2011-301940
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author Stout, Julie C
Jones, Rebecca
Labuschagne, Izelle
O'Regan, Alison M
Say, Miranda J
Dumas, Eve M
Queller, Sarah
Justo, Damian
Santos, Rachelle Dar
Coleman, Allison
Hart, Ellen P
Dürr, Alexandra
Leavitt, Blair R
Roos, Raymund A
Langbehn, Doug R
Tabrizi, Sarah J
Frost, Chris
author_facet Stout, Julie C
Jones, Rebecca
Labuschagne, Izelle
O'Regan, Alison M
Say, Miranda J
Dumas, Eve M
Queller, Sarah
Justo, Damian
Santos, Rachelle Dar
Coleman, Allison
Hart, Ellen P
Dürr, Alexandra
Leavitt, Blair R
Roos, Raymund A
Langbehn, Doug R
Tabrizi, Sarah J
Frost, Chris
author_sort Stout, Julie C
collection PubMed
description BACKGROUND: Deterioration of cognitive functioning is a debilitating symptom in many neurodegenerative diseases, such as Huntington's disease (HD). To date, there are no effective treatments for the cognitive problems associated with HD. Cognitive assessment outcomes will have a central role in the efforts to develop treatments to delay onset or slow the progression of the disease. The TRACK-HD study was designed to build a rational basis for the selection of cognitive outcomes for HD clinical trials. METHODS: There were a total of 349 participants, including controls (n=116), premanifest HD (n=117) and early HD (n=116). A standardised cognitive assessment battery (including nine cognitive tests comprising 12 outcome measures) was administered at baseline, and at 12 and 24 months, and consisted of a combination of paper and pencil and computerised tasks selected to be sensitive to cortical-striatal damage or HD. Each cognitive outcome was analysed separately using a generalised least squares regression model. Results are expressed as effect sizes to permit comparisons between tasks. RESULTS: 10 of the 12 cognitive outcomes showed evidence of deterioration in the early HD group, relative to controls, over 24 months, with greatest sensitivity in Symbol Digit, Circle Tracing direct and indirect, and Stroop word reading. In contrast, there was very little evidence of deterioration in the premanifest HD group relative to controls. CONCLUSIONS: The findings describe tests that are sensitive to longitudinal cognitive change in HD and elucidate important considerations for selecting cognitive outcomes for clinical trials of compounds aimed at ameliorating cognitive decline in HD.
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spelling pubmed-33684872012-06-07 Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease Stout, Julie C Jones, Rebecca Labuschagne, Izelle O'Regan, Alison M Say, Miranda J Dumas, Eve M Queller, Sarah Justo, Damian Santos, Rachelle Dar Coleman, Allison Hart, Ellen P Dürr, Alexandra Leavitt, Blair R Roos, Raymund A Langbehn, Doug R Tabrizi, Sarah J Frost, Chris J Neurol Neurosurg Psychiatry Cognitive Neurology BACKGROUND: Deterioration of cognitive functioning is a debilitating symptom in many neurodegenerative diseases, such as Huntington's disease (HD). To date, there are no effective treatments for the cognitive problems associated with HD. Cognitive assessment outcomes will have a central role in the efforts to develop treatments to delay onset or slow the progression of the disease. The TRACK-HD study was designed to build a rational basis for the selection of cognitive outcomes for HD clinical trials. METHODS: There were a total of 349 participants, including controls (n=116), premanifest HD (n=117) and early HD (n=116). A standardised cognitive assessment battery (including nine cognitive tests comprising 12 outcome measures) was administered at baseline, and at 12 and 24 months, and consisted of a combination of paper and pencil and computerised tasks selected to be sensitive to cortical-striatal damage or HD. Each cognitive outcome was analysed separately using a generalised least squares regression model. Results are expressed as effect sizes to permit comparisons between tasks. RESULTS: 10 of the 12 cognitive outcomes showed evidence of deterioration in the early HD group, relative to controls, over 24 months, with greatest sensitivity in Symbol Digit, Circle Tracing direct and indirect, and Stroop word reading. In contrast, there was very little evidence of deterioration in the premanifest HD group relative to controls. CONCLUSIONS: The findings describe tests that are sensitive to longitudinal cognitive change in HD and elucidate important considerations for selecting cognitive outcomes for clinical trials of compounds aimed at ameliorating cognitive decline in HD. BMJ Group 2012-05-07 2012-07 /pmc/articles/PMC3368487/ /pubmed/22566599 http://dx.doi.org/10.1136/jnnp-2011-301940 Text en © 2012, Published by the BMJ Publishing Group Limited. For permission to use (where not already granted under a licence) please go to http://group.bmj.com/group/rights-licensing/permissions. This is an open-access article distributed under the terms of the Creative Commons Attribution Non-commercial License, which permits use, distribution, and reproduction in any medium, provided the original work is properly cited, the use is non commercial and is otherwise in compliance with the license. See: http://creativecommons.org/licenses/by-nc/2.0/ and http://creativecommons.org/licenses/by-nc/2.0/legalcode.
spellingShingle Cognitive Neurology
Stout, Julie C
Jones, Rebecca
Labuschagne, Izelle
O'Regan, Alison M
Say, Miranda J
Dumas, Eve M
Queller, Sarah
Justo, Damian
Santos, Rachelle Dar
Coleman, Allison
Hart, Ellen P
Dürr, Alexandra
Leavitt, Blair R
Roos, Raymund A
Langbehn, Doug R
Tabrizi, Sarah J
Frost, Chris
Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease
title Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease
title_full Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease
title_fullStr Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease
title_full_unstemmed Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease
title_short Evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early Huntington's disease
title_sort evaluation of longitudinal 12 and 24 month cognitive outcomes in premanifest and early huntington's disease
topic Cognitive Neurology
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3368487/
https://www.ncbi.nlm.nih.gov/pubmed/22566599
http://dx.doi.org/10.1136/jnnp-2011-301940
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