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Autonomic function testing in spinocerebellar ataxia type 2
PURPOSE: To assess whether autonomic failure belongs to the clinical spectrum of spinocerebellar ataxia type 2 (SCA2), an autosomal dominant genetic disorder showing progressive cerebellar and brainstem dysfunction. METHODS: We evaluated cardiovascular autonomic function in 8 patients with SCA2 and...
Autores principales: | , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Springer Berlin Heidelberg
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995979/ https://www.ncbi.nlm.nih.gov/pubmed/29435867 http://dx.doi.org/10.1007/s10286-018-0504-4 |
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author | Indelicato, Elisabetta Fanciulli, Alessandra Ndayisaba, Jean Pierre Nachbauer, Wolfgang Granata, Roberta Wanschitz, Julia Wagner, Michaela Gizewski, Elke R. Poewe, Werner Wenning, Gregor K. Boesch, Sylvia |
author_facet | Indelicato, Elisabetta Fanciulli, Alessandra Ndayisaba, Jean Pierre Nachbauer, Wolfgang Granata, Roberta Wanschitz, Julia Wagner, Michaela Gizewski, Elke R. Poewe, Werner Wenning, Gregor K. Boesch, Sylvia |
author_sort | Indelicato, Elisabetta |
collection | PubMed |
description | PURPOSE: To assess whether autonomic failure belongs to the clinical spectrum of spinocerebellar ataxia type 2 (SCA2), an autosomal dominant genetic disorder showing progressive cerebellar and brainstem dysfunction. METHODS: We evaluated cardiovascular autonomic function in 8 patients with SCA2 and 16 age- and gender-matched healthy controls. Other autonomic domains were examined through standardized questionnaires and by testing the skin sympathetic reflex. RESULTS: Patients with SCA2 showed normal responses to cardiovascular autonomic function tests, with the exception of lower baroreflex sensitivity upon standing compared to controls. In questionnaires, 7 out of 8 patients reported bladder disturbances, while 3 out of 6 tested patients had no skin sympathetic reflex. CONCLUSIONS: We did not observe clinically overt cardiovascular autonomic failure in patients with SCA2. Other autonomic domains (i.e., bladder and sudomotor function) may be affected in the disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10286-018-0504-4) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-5995979 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | Springer Berlin Heidelberg |
record_format | MEDLINE/PubMed |
spelling | pubmed-59959792018-06-25 Autonomic function testing in spinocerebellar ataxia type 2 Indelicato, Elisabetta Fanciulli, Alessandra Ndayisaba, Jean Pierre Nachbauer, Wolfgang Granata, Roberta Wanschitz, Julia Wagner, Michaela Gizewski, Elke R. Poewe, Werner Wenning, Gregor K. Boesch, Sylvia Clin Auton Res Short Communication PURPOSE: To assess whether autonomic failure belongs to the clinical spectrum of spinocerebellar ataxia type 2 (SCA2), an autosomal dominant genetic disorder showing progressive cerebellar and brainstem dysfunction. METHODS: We evaluated cardiovascular autonomic function in 8 patients with SCA2 and 16 age- and gender-matched healthy controls. Other autonomic domains were examined through standardized questionnaires and by testing the skin sympathetic reflex. RESULTS: Patients with SCA2 showed normal responses to cardiovascular autonomic function tests, with the exception of lower baroreflex sensitivity upon standing compared to controls. In questionnaires, 7 out of 8 patients reported bladder disturbances, while 3 out of 6 tested patients had no skin sympathetic reflex. CONCLUSIONS: We did not observe clinically overt cardiovascular autonomic failure in patients with SCA2. Other autonomic domains (i.e., bladder and sudomotor function) may be affected in the disease. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1007/s10286-018-0504-4) contains supplementary material, which is available to authorized users. Springer Berlin Heidelberg 2018-02-12 2018 /pmc/articles/PMC5995979/ /pubmed/29435867 http://dx.doi.org/10.1007/s10286-018-0504-4 Text en © The Author(s) 2018 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 | Short Communication Indelicato, Elisabetta Fanciulli, Alessandra Ndayisaba, Jean Pierre Nachbauer, Wolfgang Granata, Roberta Wanschitz, Julia Wagner, Michaela Gizewski, Elke R. Poewe, Werner Wenning, Gregor K. Boesch, Sylvia Autonomic function testing in spinocerebellar ataxia type 2 |
title | Autonomic function testing in spinocerebellar ataxia type 2 |
title_full | Autonomic function testing in spinocerebellar ataxia type 2 |
title_fullStr | Autonomic function testing in spinocerebellar ataxia type 2 |
title_full_unstemmed | Autonomic function testing in spinocerebellar ataxia type 2 |
title_short | Autonomic function testing in spinocerebellar ataxia type 2 |
title_sort | autonomic function testing in spinocerebellar ataxia type 2 |
topic | Short Communication |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC5995979/ https://www.ncbi.nlm.nih.gov/pubmed/29435867 http://dx.doi.org/10.1007/s10286-018-0504-4 |
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