Literature DB >> 31912433

Selective Procedural Memory Impairment but Preserved Declarative Memory in Spinocerebellar Ataxia Type 3.

Zohar Elyoseph1, Matti Mintz1,2, Eli Vakil3,4, Roy Zaltzman5,6, Carlos R Gordon7,8,9.   

Abstract

Spinocerebellar ataxia type 3 (SCA3), also known as Machado-Joseph disease, is an autosomal dominant neurodegenerative disorder that affects mainly the cerebellum and less other brain areas. While the ataxic/motor features of the disease have been well described, the cognitive consequences of the degeneration require additional testing. The aim of this study was to evaluate learning abilities in SCA3. We tested 13 SCA3 patients and 14 age-matched healthy controls, all of Yemenite origin, on a neuropsychological battery of procedural and declarative memory tests. SCA3 patients demonstrated impaired sequence learning on the procedural Serial Reaction Time test (SRTt) but normal learning on the procedural Weather Prediction Probabilistic Classification test (WPPCt). SCA3 patients showed normal learning on the declarative Rey Auditory Verbal Learning test (Rey-AVLt). The correlations between the learning measures of the SRTt, WPPCt, and Rey-AVLt tests in SCA3 and controls separately were not significant. These results imply that the cerebellar degeneration in SCA3 causes selective impairment in procedural sequence learning while the procedural probabilistic learning and declarative memory were mostly preserved. These findings support the assumption that procedural learning is not a homogeneous function and could be dissociated in cerebellar neurodegenerative disease.

Entities:  

Keywords:  Cerebellum; Declarative tests; Machado-Joseph disease; Procedural tests; SCA3

Mesh:

Year:  2020        PMID: 31912433     DOI: 10.1007/s12311-019-01101-w

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  56 in total

1.  Dissociation between two types of skill learning tasks: the differential effect of divided attention.

Authors:  Eli Vakil; Yaakov Hoffman
Journal:  J Clin Exp Neuropsychol       Date:  2004-08       Impact factor: 2.475

2.  Cerebral cortex involvement in Machado-Joseph disease.

Authors:  T J R de Rezende; A D'Abreu; R P Guimarães; T M Lopes; I Lopes-Cendes; F Cendes; G Castellano; M C França
Journal:  Eur J Neurol       Date:  2014-09-23       Impact factor: 6.089

3.  Scale for the assessment and rating of ataxia: development of a new clinical scale.

Authors:  T Schmitz-Hübsch; S Tezenas du Montcel; L Baliko; J Berciano; S Boesch; C Depondt; P Giunti; C Globas; J Infante; J-S Kang; B Kremer; C Mariotti; B Melegh; M Pandolfo; M Rakowicz; P Ribai; R Rola; L Schöls; S Szymanski; B P van de Warrenburg; A Dürr; T Klockgether; Roberto Fancellu
Journal:  Neurology       Date:  2006-06-13       Impact factor: 9.910

Review 4.  The wide spectrum of spinocerebellar ataxias (SCAs).

Authors:  Mario-Ubaldo Manto
Journal:  Cerebellum       Date:  2005       Impact factor: 3.847

5.  Dissociation of habit-learning in Parkinson's and cerebellar disease.

Authors:  K Witt; A Nuhsman; G Deuschl
Journal:  J Cogn Neurosci       Date:  2002-04-01       Impact factor: 3.225

6.  Procedural learning in Parkinson's disease and cerebellar degeneration.

Authors:  A Pascual-Leone; J Grafman; K Clark; M Stewart; S Massaquoi; J S Lou; M Hallett
Journal:  Ann Neurol       Date:  1993-10       Impact factor: 10.422

7.  A dominant hereditary ataxia resembling Machado-Joseph disease in Arnhem Land, Australia.

Authors:  T Burt; P Blumbergs; B Currie
Journal:  Neurology       Date:  1993-09       Impact factor: 9.910

8.  Autosomal dominant system degeneration in Portuguese families of the Azores Islands. A new genetic disorder involving cerebellar, pyramidal, extrapyramidal and spinal cord motor functions.

Authors:  P Coutinho; C Andrade
Journal:  Neurology       Date:  1978-07       Impact factor: 9.910

Review 9.  The hereditary ataxias.

Authors:  A H Koeppen
Journal:  J Neuropathol Exp Neurol       Date:  1998-06       Impact factor: 3.685

10.  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

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  1 in total

Review 1.  Neurocognitive Changes in Spinocerebellar Ataxia Type 3: A Systematic Review with a Narrative Design.

Authors:  Kah Hui Yap; Roy P C Kessels; Shahrul Azmin; Bart van de Warrenburg; Norlinah Mohamed Ibrahim
Journal:  Cerebellum       Date:  2021-07-07       Impact factor: 3.648

  1 in total

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