Fronto-striatal gray matter contributions to discrimination learning in Parkinson's disease

被引:12
|
作者
O'Callaghan, Claire [1 ,2 ]
Moustafa, Ahmed A. [3 ,4 ]
de Wit, Sanne [5 ,6 ]
Shine, James M. [7 ]
Robbins, Trevor W. [8 ]
Lewis, Simon J. G. [7 ]
Hornberger, Michael [1 ,2 ,9 ,10 ]
机构
[1] Neurosci Res Australia, Sydney, NSW 2031, Australia
[2] Univ New S Wales, Fac Med, Sch Med Sci, Sydney, NSW, Australia
[3] Univ Western Sydney, Sch Social Sci & Psychol, Sydney, NSW, Australia
[4] Univ Western Sydney, Marcs Inst Brain & Behav, Sydney, NSW, Australia
[5] Univ Amsterdam, Cognit Sci Ctr Amsterdam, Amsterdam, Netherlands
[6] Univ Amsterdam, Dept Clin Psychol, NL-1018 WB Amsterdam, Netherlands
[7] Univ Sydney, Parkinsons Dis Clin, Brain & Mind Res Inst, Sydney, NSW 2006, Australia
[8] Univ Cambridge, Dept Psychol, Behav & Clin Neurosci Inst, Cambridge, England
[9] ARC Ctr Excellence Cognit & Its Disorders, Sydney, NSW, Australia
[10] Univ Cambridge, Dept Clin Neurosci, Cambridge, England
基金
英国医学研究理事会; 澳大利亚研究理事会;
关键词
Parkinson's disease; discrimination learning; goal-directed learning; computational modeling; voxel-based morphometry; fronto-striatal; VOXEL-BASED MORPHOMETRY; BASAL GANGLIA; MOTIVATIONAL CONTROL; PREFRONTAL CORTEX; DOPAMINE; DEFICITS; REWARD; FEEDBACK; BEHAVIOR; ATROPHY;
D O I
10.3389/fncom.2013.00180
中图分类号
Q [生物科学];
学科分类号
07 ; 0710 ; 09 ;
摘要
Discrimination learning deficits in Parkinson's disease (PD) have been well-established. Using both behavioral patient studies and computational approaches, these deficits have typically been attributed to dopamine imbalance across the basal ganglia. However, this explanation of impaired learning in PD does not account for the possible contribution of other pathological changes that occur in the disease process, importantly including gray matter loss. To address this gap in the literature, the current study explored the relationship between fronto-striatal gray matter atrophy and learning in PD. We employed a discrimination learning task and computational modeling in order to assess learning rates in non-demented PD patients. Behaviorally, we confirmed that learning rates were reduced in patients relative to controls. Furthermore, voxel-based morphometry imaging analysis demonstrated that this learning impairment was directly related to gray matter loss in discrete fronto-striatal regions (specifically, the ventromedial prefrontal cortex, inferior frontal gyrus and nucleus accumbens). These findings suggest that dopaminergic imbalance may not be the sole determinant of discrimination learning deficits in PD, and highlight the importance of factoring in the broader pathological changes when constructing models of learning in PD.
引用
收藏
页码:1 / 10
页数:10
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