Literature DB >> 23736996

Progressive cognitive dysfunction in spinocerebellar ataxia type 3.

Sandra Roeske1, Ina Filla, Stefan Heim, Katrin Amunts, Christoph Helmstaedter, Ullrich Wüllner, Michael Wagner, Thomas Klockgether, Martina Minnerop.   

Abstract

BACKGROUND: Although it is well established that there is cognitive dysfunction in spinocerebellar ataxia type 3 (SCA3), it is unknown whether cognition deteriorates with disease progression. We therefore prospectively studied cognitive function in patients with SCA3.
METHODS: Eleven patients with SCA3 were assessed using an extensive neuropsychological test battery and retested after 3.5 ± 0.4 years.
RESULTS: In addition to ataxia and motor control, verbal learning and verbal and figural memory deteriorated significantly during the follow-up period. An increase in depressive symptoms was not observed.
CONCLUSIONS: The observation that memory and learning abilities deteriorated with disease progression suggests that cognitive dysfunction is an integral part of SCA3. Because the applied tests for memory function did not require motor responses, cognitive decline cannot be attributed to progressive cerebellar ataxia. The deterioration of verbal and figural memory can be explained either by extracerebellar pathology or by disruption of cerebellar-cerebral circuitries.
© 2013 International Parkinson and Movement Disorder Society.

Entities:  

Keywords:  SCA3; ataxia; cerebellum; cognition; follow-up

Mesh:

Year:  2013        PMID: 23736996     DOI: 10.1002/mds.25512

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  17 in total

1.  Cognition in SCA21 reflects developmental and adult onset cerebellar cognitive affective syndrome.

Authors:  Pedro Braga-Neto; José Luiz Pedroso; Orlando G P Barsottini; Jeremy D Schmahmann
Journal:  Brain       Date:  2015-01-08       Impact factor: 13.501

Review 2.  Fragile X-associated tremor/ataxia syndrome: phenotypic comparisons with other movement disorders.

Authors:  Erin E Robertson; Deborah A Hall; Andrew R McAsey; Joan A O'Keefe
Journal:  Clin Neuropsychol       Date:  2016-08       Impact factor: 3.535

3.  Neurophysiological studies and non-motor symptoms prior to ataxia in a patient with machado-joseph disease: trying to understand the natural history of brain degeneration.

Authors:  José Luiz Pedroso; Edson Bor-Seng-Shu; Pedro Braga-Neto; Rodrigo Souza Ribeiro; Márcio Luiz Escorcio Bezerra; Lucila B F do Prado; Ilza Rosa Batista; Helena Alessi; Manoel Jacobsen Teixeira; Gilberto Mastrocola Manzano; Gilmar Fernandes do Prado; Orlando Graziani Povoas Barsottini
Journal:  Cerebellum       Date:  2014-08       Impact factor: 3.847

4.  Nonmotor Symptoms in Patients with Spinocerebellar Ataxia Type 10.

Authors:  Adriana Moro; Renato P Munhoz; Mariana Moscovich; Walter O Arruda; Salmo Raskin; Laura Silveira-Moriyama; Tetsuo Ashizawa; Hélio A G Teive
Journal:  Cerebellum       Date:  2017-12       Impact factor: 3.847

5.  A knockin mouse model of spinocerebellar ataxia type 3 exhibits prominent aggregate pathology and aberrant splicing of the disease gene transcript.

Authors:  Biswarathan Ramani; Ginny M Harris; Rogerio Huang; Takahiro Seki; Geoffrey G Murphy; Maria do Carmo Costa; Svetlana Fischer; Thomas L Saunders; Guangbin Xia; Richard C McEachin; Henry L Paulson
Journal:  Hum Mol Genet       Date:  2014-10-15       Impact factor: 6.150

6.  Executive dysfunction in patients with spinocerebellar ataxia type 3.

Authors:  Itaru Tamura; Asako Takei; Shinsuke Hamada; Hiroyuki Soma; Michio Nonaka; Sanae Homma; Fumio Moriwaka
Journal:  J Neurol       Date:  2018-05-03       Impact factor: 4.849

7.  The CCAS-scale in hereditary ataxias: helpful on the group level, particularly in SCA3, but limited in individual patients.

Authors:  Sandra Roeske; Dagmar Timmann; Andreas Thieme; Jennifer Faber; Patricia Sulzer; Kathrin Reetz; Imis Dogan; Miriam Barkhoff; Janna Krahe; Heike Jacobi; Julia-Elisabeth Aktories; Martina Minnerop; Saskia Elben; Raquel van der Veen; Johanna Müller; Giorgi Batsikadze; Jürgen Konczak; Matthis Synofzik
Journal:  J Neurol       Date:  2022-04-01       Impact factor: 6.682

8.  Change in the cortical complexity of spinocerebellar ataxia type 3 appears earlier than clinical symptoms.

Authors:  Tzu-Yun Wang; Chii-Wen Jao; Bing-Wen Soong; Hsiu-Mei Wu; Kuo-Kai Shyu; Po-Shan Wang; Yu-Te Wu
Journal:  PLoS One       Date:  2015-04-21       Impact factor: 3.240

9.  A longitudinal investigation into cognition and disease progression in spinocerebellar ataxia types 1, 2, 3, 6, and 7.

Authors:  Amy Moriarty; Arron Cook; Helen Hunt; Matthew E Adams; Lisa Cipolotti; Paola Giunti
Journal:  Orphanet J Rare Dis       Date:  2016-06-22       Impact factor: 4.123

Review 10.  Cognitive Changes in the Spinocerebellar Ataxias Due to Expanded Polyglutamine Tracts: A Survey of the Literature.

Authors:  Evelyn Lindsay; Elsdon Storey
Journal:  Brain Sci       Date:  2017-07-14
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