Literature DB >> 24525517

Cognitive impairment in native Chinese with spinocerebellar ataxia type 3.

Li Feng1, Ding Bang Chen, Le Hou, Lin Huan Huang, Shu Yang Lu, Xiu Ling Liang, Xun Hua Li.   

Abstract

BACKGROUND: Previous studies have shown cognitive impairment in patients with spinocerebellar ataxia type 3 (SCA3). However, there is a lack of data on Chinese patients with SCA3.
METHOD: We investigated 22 native Chinese with SCA3 and 18 controls matched for age, education as well as mental status. Cognitive assessments were carefully carried out to measure verbal fluency, memory, attention, executive function, visuospatial and visuoconstructive functions.
RESULTS: The most common impairments of cognition in native Chinese with SCA3 were disruption of phonemic verbal fluency and frontal executive dysfunction. Deficits in semantic fluency were detected in about 31.8% patients. Impaired visuospatial function and verbal memory were also found in native Chinese with SCA3. The degree of ataxia, CAG repeat length and education were found to correlate with cognitive performance. Multivariate binary logistic regression suggested that an oculomotor disorder and depression are predictors of cognitive impairment.
CONCLUSION: Native Chinese with SCA3 had cognitive impairment of frontal executive function, temporal and parietal functions. An oculomotor disorder might be an index of cognitive dysfunction.
© 2014 S. Karger AG, Basel.

Entities:  

Mesh:

Year:  2014        PMID: 24525517     DOI: 10.1159/000357404

Source DB:  PubMed          Journal:  Eur Neurol        ISSN: 0014-3022            Impact factor:   1.710


  7 in total

1.  Oculomotor deficits in spinocerebellar ataxia type 3: Potential biomarkers of preclinical detection and disease progression.

Authors:  Chao Wu; Ding-Bang Chen; Li Feng; Xiang-Xue Zhou; Ji-Wei Zhang; Hua-Jing You; Xiu-Ling Liang; Zhong Pei; Xun-Hua Li
Journal:  CNS Neurosci Ther       Date:  2017-02-13       Impact factor: 5.243

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.  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

4.  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

Review 5.  Linking Essential Tremor to the Cerebellum: Clinical Evidence.

Authors:  Julián Benito-León; Andrés Labiano-Fontcuberta
Journal:  Cerebellum       Date:  2016-06       Impact factor: 3.847

Review 6.  Nonmotor symptoms in spinocerebellar ataxias (SCAs).

Authors:  Adriana Moro; Mariana Moscovich; Marina Farah; Carlos Henrique F Camargo; Hélio A G Teive; Renato P Munhoz
Journal:  Cerebellum Ataxias       Date:  2019-08-27

Review 7.  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

  7 in total

北京卡尤迪生物科技股份有限公司 © 2022-2023.