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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...

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Detalles Bibliográficos
Autores principales: 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
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Springer Berlin Heidelberg 2018
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
Descripción
Sumario: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.