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Cognitive and social cognitive functioning in spinocerebellar ataxia: a preliminary characterization

Cognitive and social cognitive functioning in spinocerebellar ataxia: a preliminary characterization
Cognitive and social cognitive functioning in spinocerebellar ataxia: a preliminary characterization
Introduction The spinocerebellar ataxias (SCAs), are rare neurodegenerative disorders caused by distinct genetic mutations. Clinically, the SCAs are characterised by progressive ataxia and a variety of other features, including cognitive dysfunction. The latter is consistent with a growing body of evidence supporting a cognitive as well as motor role for the cerebellum. Recent suggestions of cerebellar involvement in social cognition have not been extensively explored in these conditions. The availability of definitive molecular diagnosis allows genetically defined subgroups of SCA patients, with distinct patterns of cerebellar and extracerebellar involvement, to be tested comparatively using a common battery of tests of general, social and emotional cognition. Methods: Nine patients with SCA6, and 6 with SCA3 were assessed using a comprehensive battery of neuropsychological instruments, encompassing domains of memory, language, visuo-spatial skills, calculation, attention and executive function, emotional processing and theory of mind (ToM). Results There were no deficits in visuo-spatial processing or calculation in either group, while individuals with naming and attentional difficulties were seen in both. Deficits in memory and executive function were present in both conditions, albeit more pronounced in SCA3. By contrast, both groups demonstrated consistently poor performance on ToM tests, and normal attribution of social and emotional responses. Conclusion The data support the hypothesis that the cerebellum is important for cognitive as well as motor activity. The pattern of overlap of domain impairments provides tentative preliminary evidence that there is a cerebellar contribution to aspects of memory and executive function and ToM, and that other domains depend more on neural system outside the cerebellum. The findings relating to ToM are relevant to the possibility of cerebellar involvement in autism.
cognitive functioning, social cognitive functioning, spinocerebellar ataxias, neurodegenerative disorders, genetic mutations
0340-5354
398-405
Garrard, P.
4815434c-b90e-4998-934b-794c741eea76
Martin, N.H.
9723e167-061a-4a8c-afd1-7e142b967fa1
Giunti, P.
b292b807-7e8b-496e-a3cc-d3471438e10f
Cipolotti, L.
fa90bd6b-a3c1-46a5-b5fd-32acdbb1332a
Garrard, P.
4815434c-b90e-4998-934b-794c741eea76
Martin, N.H.
9723e167-061a-4a8c-afd1-7e142b967fa1
Giunti, P.
b292b807-7e8b-496e-a3cc-d3471438e10f
Cipolotti, L.
fa90bd6b-a3c1-46a5-b5fd-32acdbb1332a

Garrard, P., Martin, N.H., Giunti, P. and Cipolotti, L. (2008) Cognitive and social cognitive functioning in spinocerebellar ataxia: a preliminary characterization. Journal of Neurology, 255 (3), 398-405. (doi:10.1007/s00415-008-0680-6).

Record type: Article

Abstract

Introduction The spinocerebellar ataxias (SCAs), are rare neurodegenerative disorders caused by distinct genetic mutations. Clinically, the SCAs are characterised by progressive ataxia and a variety of other features, including cognitive dysfunction. The latter is consistent with a growing body of evidence supporting a cognitive as well as motor role for the cerebellum. Recent suggestions of cerebellar involvement in social cognition have not been extensively explored in these conditions. The availability of definitive molecular diagnosis allows genetically defined subgroups of SCA patients, with distinct patterns of cerebellar and extracerebellar involvement, to be tested comparatively using a common battery of tests of general, social and emotional cognition. Methods: Nine patients with SCA6, and 6 with SCA3 were assessed using a comprehensive battery of neuropsychological instruments, encompassing domains of memory, language, visuo-spatial skills, calculation, attention and executive function, emotional processing and theory of mind (ToM). Results There were no deficits in visuo-spatial processing or calculation in either group, while individuals with naming and attentional difficulties were seen in both. Deficits in memory and executive function were present in both conditions, albeit more pronounced in SCA3. By contrast, both groups demonstrated consistently poor performance on ToM tests, and normal attribution of social and emotional responses. Conclusion The data support the hypothesis that the cerebellum is important for cognitive as well as motor activity. The pattern of overlap of domain impairments provides tentative preliminary evidence that there is a cerebellar contribution to aspects of memory and executive function and ToM, and that other domains depend more on neural system outside the cerebellum. The findings relating to ToM are relevant to the possibility of cerebellar involvement in autism.

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More information

Published date: March 2008
Keywords: cognitive functioning, social cognitive functioning, spinocerebellar ataxias, neurodegenerative disorders, genetic mutations

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Local EPrints ID: 62385
URI: http://eprints.soton.ac.uk/id/eprint/62385
ISSN: 0340-5354
PURE UUID: 4fa0fa2b-0b37-4d34-9bcd-bb53491ac3c2

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Date deposited: 21 Apr 2009
Last modified: 15 Mar 2024 11:30

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Contributors

Author: P. Garrard
Author: N.H. Martin
Author: P. Giunti
Author: L. Cipolotti

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