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Progression of motor subtypes in Huntington’s disease: a 6-year follow-up study

The objective of this study is to investigate the progression of predominantly choreatic and hypokinetic-rigid signs in Huntington’s disease (HD) and their relationship with cognitive and general functioning over time. The motor signs in HD can be divided into predominantly choreatic and hypokinetic...

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Autores principales: Jacobs, M., Hart, E. P., van Zwet, E. W., Bentivoglio, A. R., Burgunder, J. M., Craufurd, D., Reilmann, R., Saft, C., Roos, R. A. C.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037142/
https://www.ncbi.nlm.nih.gov/pubmed/27435968
http://dx.doi.org/10.1007/s00415-016-8233-x
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author Jacobs, M.
Hart, E. P.
van Zwet, E. W.
Bentivoglio, A. R.
Burgunder, J. M.
Craufurd, D.
Reilmann, R.
Saft, C.
Roos, R. A. C.
author_facet Jacobs, M.
Hart, E. P.
van Zwet, E. W.
Bentivoglio, A. R.
Burgunder, J. M.
Craufurd, D.
Reilmann, R.
Saft, C.
Roos, R. A. C.
author_sort Jacobs, M.
collection PubMed
description The objective of this study is to investigate the progression of predominantly choreatic and hypokinetic-rigid signs in Huntington’s disease (HD) and their relationship with cognitive and general functioning over time. The motor signs in HD can be divided into predominantly choreatic and hypokinetic-rigid subtypes. It has been reported in cross-sectional studies that predominantly choreatic HD patients perform better on functional and cognitive assessments compared to predominantly hypokinetic-rigid HD patients. The course of these motor subtypes and their clinical profiles has not been investigated longitudinally. A total of 4135 subjects who participated in the European HD Network REGISTRY study were included and classified at baseline as either predominantly choreatic (n = 891), hypokinetic-rigid (n = 916), or mixed-motor (n = 2328), based on a previously used method. The maximum follow-up period was 6 years. The mixed-motor group was not included in the analyses. Linear mixed models were constructed to investigate changes in motor subtypes over time and their relationship with cognitive and functional decline. Over the 6-year follow-up period, the predominantly choreatic group showed a significant decrease in chorea, while hypokinetic-rigid symptoms slightly increased in the hypokinetic-rigid group. On the Total Functional Capacity, Stroop test, and Verbal fluency task the rate of change over time was significantly faster in the predominantly choreatic group, while on all other clinical assessments the decline was comparable for both groups. Our results suggest that choreatic symptoms decrease over time, whereas hypokinetic-rigid symptoms slightly increase in a large cohort of HD patients. Moreover, different motor subtypes can be related to different clinical profiles. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00415-016-8233-x) contains supplementary material, which is available to authorized users.
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spelling pubmed-50371422016-10-11 Progression of motor subtypes in Huntington’s disease: a 6-year follow-up study Jacobs, M. Hart, E. P. van Zwet, E. W. Bentivoglio, A. R. Burgunder, J. M. Craufurd, D. Reilmann, R. Saft, C. Roos, R. A. C. J Neurol Original Communication The objective of this study is to investigate the progression of predominantly choreatic and hypokinetic-rigid signs in Huntington’s disease (HD) and their relationship with cognitive and general functioning over time. The motor signs in HD can be divided into predominantly choreatic and hypokinetic-rigid subtypes. It has been reported in cross-sectional studies that predominantly choreatic HD patients perform better on functional and cognitive assessments compared to predominantly hypokinetic-rigid HD patients. The course of these motor subtypes and their clinical profiles has not been investigated longitudinally. A total of 4135 subjects who participated in the European HD Network REGISTRY study were included and classified at baseline as either predominantly choreatic (n = 891), hypokinetic-rigid (n = 916), or mixed-motor (n = 2328), based on a previously used method. The maximum follow-up period was 6 years. The mixed-motor group was not included in the analyses. Linear mixed models were constructed to investigate changes in motor subtypes over time and their relationship with cognitive and functional decline. Over the 6-year follow-up period, the predominantly choreatic group showed a significant decrease in chorea, while hypokinetic-rigid symptoms slightly increased in the hypokinetic-rigid group. On the Total Functional Capacity, Stroop test, and Verbal fluency task the rate of change over time was significantly faster in the predominantly choreatic group, while on all other clinical assessments the decline was comparable for both groups. Our results suggest that choreatic symptoms decrease over time, whereas hypokinetic-rigid symptoms slightly increase in a large cohort of HD patients. Moreover, different motor subtypes can be related to different clinical profiles. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1007/s00415-016-8233-x) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2016-07-19 2016 /pmc/articles/PMC5037142/ /pubmed/27435968 http://dx.doi.org/10.1007/s00415-016-8233-x Text en © The Author(s) 2016 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided 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.
spellingShingle Original Communication
Jacobs, M.
Hart, E. P.
van Zwet, E. W.
Bentivoglio, A. R.
Burgunder, J. M.
Craufurd, D.
Reilmann, R.
Saft, C.
Roos, R. A. C.
Progression of motor subtypes in Huntington’s disease: a 6-year follow-up study
title Progression of motor subtypes in Huntington’s disease: a 6-year follow-up study
title_full Progression of motor subtypes in Huntington’s disease: a 6-year follow-up study
title_fullStr Progression of motor subtypes in Huntington’s disease: a 6-year follow-up study
title_full_unstemmed Progression of motor subtypes in Huntington’s disease: a 6-year follow-up study
title_short Progression of motor subtypes in Huntington’s disease: a 6-year follow-up study
title_sort progression of motor subtypes in huntington’s disease: a 6-year follow-up study
topic Original Communication
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5037142/
https://www.ncbi.nlm.nih.gov/pubmed/27435968
http://dx.doi.org/10.1007/s00415-016-8233-x
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