Dopaminergic basis for deficits in working memory but not attentional set-shifting in Parkinson's disease

被引:235
作者
Lewis, SJG
Slabosz, A
Robbins, TW
Barker, RA
Owen, AM
机构
[1] Addenbrookes Hosp, Cambridge Ctr Brain Repair, Cambridge CB2 2PY, England
[2] Univ Cambridge, Dept Neurol, Cambridge, England
[3] MRC, Cognit & Brain Sci Unit, Cambridge, England
[4] Univ Cambridge, Dept Expt Psychol, Cambridge CB2 3EB, England
[5] Jagiellonian Univ, Inst Psychol, Krakow, Poland
关键词
working memory; Parkinson's disease; dopamine; caudate nuclei; frontal lobes; basal ganglia;
D O I
10.1016/j.neuropsychologia.2004.10.001
中图分类号
B84 [心理学]; C [社会科学总论]; Q98 [人类学];
学科分类号
03 ; 0303 ; 030303 ; 04 ; 0402 ;
摘要
Although Parkinson's disease is a common neurodegenerative disorder characterised by its motoric symptoms, there is an increasing recognition of accompanying impairments in cognition that have a profound impact on the quality of life of these patients. These deficits predominantly affect executive function and impairments of working memory have been frequently reported. However, the underlying neurochemical and pathological basis for these deficits are not well understood. In this study, 20 patients were tested 'on' and 'off' levodopa (L-dopa) medication on a task that allowed different aspects of working memory function such as maintenance, retrieval and manipulation to be tested within the same general paradigm as well as on an unrelated test of attentional set-shifting, which is known to be sensitive to deficits in early Parkinson's disease. Compared to healthy volunteers, PD patients were impaired at manipulation more than maintenance or retrieval of information within working memory. The patients were also impaired at the attentional set-shifting task. However, whereas L-dopa ameliorated the working memory deficit in manipulation (improving both accuracy and cognitive response time), it had no effect on the attentional set-shifting impairment. These results confirm that working memory deficits in PD are both psychologically specific and related to dopamine depletion. It is anticipated that greater understanding of these mechanisms will lead to future therapeutic improvements. (c) 2004 Elsevier Ltd. All rights reserved.
引用
收藏
页码:823 / 832
页数:10
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