Specific cognitive deficits in mild frontal variant frontotemporal dementia

被引:290
作者
Rahman, S
Sahakian, BJ
Hodges, JR
Rogers, RD
Robbins, TW
机构
[1] Univ Cambridge, Dept Psychiat, Cambridge, England
[2] Univ Cambridge, Dept Neurol, Cambridge, England
[3] Univ Cambridge, MRC, Cognit & Brain Sci Unit, Cambridge, England
[4] Univ Cambridge, Dept Expt Psychol, Cambridge CB2 3EB, England
[5] Univ Cambridge, MRC, Ctr Brain Repair, Cambridge, England
基金
英国惠康基金;
关键词
frontotemporal dementia; decision-making; reversal learning; orbitofrontal prefrontal cortex; ventromedial prefrontal cortex;
D O I
10.1093/brain/122.8.1469
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Eight patients with relatively mild frontal variant frontotemporal dementia (fvFTD) were compared with age- and IQ-matched control volunteers on tests of executive and mnemonic function. Tests of pattern and spatial recognition memory, spatial span, spatial working memory, planning, visual discrimination learning/attentional set-shifting and decision-making were employed. Patients with fvFTD were found to have deficits in the visual discrimination learning paradigm specific to the reversal stages. Furthermore, in the decision-making paradigm, patients were found to show genuine risk-taking behaviour with increased deliberation times rather than merely impulsive behaviour. It was especially notable that these patients demonstrated virtually no deficits in other tests that have also been shown to be sensitive to frontal lobe dysfunction, such as the spatial working memory and planning tasks. These results are discussed in relation to the possible underlying neuropathology, the anatomical connectivity and the hypothesized heterogeneous functions of areas of the prefrontal cortex. In particular, given the nature of the cognitive deficits demonstrated by these patients, we postulate that, relatively early in the course of the disease, the ventromedial (or orbitofrontal) cortex is a major locus of dysfunction and that this may relate to the behavioural presentation of these patients clinically described in the individual case histories.
引用
收藏
页码:1469 / 1493
页数:25
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