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Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit

BACKGROUND: Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder that affects the cerebellar system and other subcortical regions of the brain. As for other cerebellar diseases, the severity of this type of ataxia can be assessed with the Scale for Assessment and Rating of Ataxia (SA...

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Autores principales: Pulido-Valdeolivas, Irene, Gómez-Andrés, David, Sanz-Gallego, Irene, Rausell, Estrella, Arpa, Javier
Formato: Online Artículo Texto
Lenguaje:English
Publicado: BioMed Central 2016
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763420/
https://www.ncbi.nlm.nih.gov/pubmed/26909158
http://dx.doi.org/10.1186/s40673-016-0042-6
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author Pulido-Valdeolivas, Irene
Gómez-Andrés, David
Sanz-Gallego, Irene
Rausell, Estrella
Arpa, Javier
author_facet Pulido-Valdeolivas, Irene
Gómez-Andrés, David
Sanz-Gallego, Irene
Rausell, Estrella
Arpa, Javier
author_sort Pulido-Valdeolivas, Irene
collection PubMed
description BACKGROUND: Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder that affects the cerebellar system and other subcortical regions of the brain. As for other cerebellar diseases, the severity of this type of ataxia can be assessed with the Scale for Assessment and Rating of Ataxia (SARA) which gives a total score that reflects functional impairment out of 8 cerebellar function tests. SCA3 patients score profile is heterogeneous on at the start of follow up. This study investigates possible patterns in those profiles and analyses the impact of other usually concurrent signs of impairment of extracerebellar motor systems in that profile variability by means of multivariate statistical approaches. METHODS: Seventeen patients with SCA3 underwent systematic anamnesis, neurological and SARA assessment, visual evaluation of (123)I-Ioflupane (DaTSCAN) single-photon emission computed tomography (SPECT) imaging and electrophysiological studies (nerve conduction and electromyography). Patterns in the profiles of SARA item scores were investigated by hierarchical clustering after multivariate correspondence analysis. A network analysis was used to represent relationships between SARA item scores, clinical, genetic and neurological examination parameters as well as abnormalities of DaTSCAN SPECT imaging and electrophysiological studies. RESULTS: The most frequently altered SARA items in all patients are gait and stance, and three profiles of SCA3 patients can be distinguished depending mainly on their degree of impairment in those two items. Other SARA items like the score on heel-shin slide contribute less to the classification. Network analysis shows that SARA item scores configure a single domain that is independent of the size of the mutated expanded allele and age of onset, which are, in turn closely and inversely correlated. The severity of cerebellar dysfunction is correlated with longer disease duration, altered visual evaluation of DaTSCAN SPECT imaging and decreased patellar reflexes. Neither the presence of pyramidal or extrapyramidal signs nor the intensity of polyneuropathy is correlated with the SARA items scores. CONCLUSIONS: Pattern recognition approaches are useful tools to describe clinical phenotypes of ataxias and to identify particular configurations of cerebellar signs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40673-016-0042-6) contains supplementary material, which is available to authorized users.
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spelling pubmed-47634202016-02-24 Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit Pulido-Valdeolivas, Irene Gómez-Andrés, David Sanz-Gallego, Irene Rausell, Estrella Arpa, Javier Cerebellum Ataxias Research BACKGROUND: Spinocerebellar ataxia type 3 (SCA3) is a neurodegenerative disorder that affects the cerebellar system and other subcortical regions of the brain. As for other cerebellar diseases, the severity of this type of ataxia can be assessed with the Scale for Assessment and Rating of Ataxia (SARA) which gives a total score that reflects functional impairment out of 8 cerebellar function tests. SCA3 patients score profile is heterogeneous on at the start of follow up. This study investigates possible patterns in those profiles and analyses the impact of other usually concurrent signs of impairment of extracerebellar motor systems in that profile variability by means of multivariate statistical approaches. METHODS: Seventeen patients with SCA3 underwent systematic anamnesis, neurological and SARA assessment, visual evaluation of (123)I-Ioflupane (DaTSCAN) single-photon emission computed tomography (SPECT) imaging and electrophysiological studies (nerve conduction and electromyography). Patterns in the profiles of SARA item scores were investigated by hierarchical clustering after multivariate correspondence analysis. A network analysis was used to represent relationships between SARA item scores, clinical, genetic and neurological examination parameters as well as abnormalities of DaTSCAN SPECT imaging and electrophysiological studies. RESULTS: The most frequently altered SARA items in all patients are gait and stance, and three profiles of SCA3 patients can be distinguished depending mainly on their degree of impairment in those two items. Other SARA items like the score on heel-shin slide contribute less to the classification. Network analysis shows that SARA item scores configure a single domain that is independent of the size of the mutated expanded allele and age of onset, which are, in turn closely and inversely correlated. The severity of cerebellar dysfunction is correlated with longer disease duration, altered visual evaluation of DaTSCAN SPECT imaging and decreased patellar reflexes. Neither the presence of pyramidal or extrapyramidal signs nor the intensity of polyneuropathy is correlated with the SARA items scores. CONCLUSIONS: Pattern recognition approaches are useful tools to describe clinical phenotypes of ataxias and to identify particular configurations of cerebellar signs. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (doi:10.1186/s40673-016-0042-6) contains supplementary material, which is available to authorized users. BioMed Central 2016-02-23 /pmc/articles/PMC4763420/ /pubmed/26909158 http://dx.doi.org/10.1186/s40673-016-0042-6 Text en © Pulido-Valdeolivas et al. 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. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated.
spellingShingle Research
Pulido-Valdeolivas, Irene
Gómez-Andrés, David
Sanz-Gallego, Irene
Rausell, Estrella
Arpa, Javier
Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit
title Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit
title_full Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit
title_fullStr Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit
title_full_unstemmed Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit
title_short Patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit
title_sort patterns of motor signs in spinocerebellar ataxia type 3 at the start of follow-up in a reference unit
topic Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC4763420/
https://www.ncbi.nlm.nih.gov/pubmed/26909158
http://dx.doi.org/10.1186/s40673-016-0042-6
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