Functional MRI study of a serial reaction time task in Huntington's disease

被引:61
作者
Kim, JS
Reading, SAJ
Brashers-Krug, T
Calhoun, VD
Ross, CA
Pearlson, GD
机构
[1] Hartford Hosp, Inst Living, Olin Neuropsychiat Res Ctr, Hartford, CT 06106 USA
[2] Yale Univ, Sch Med, Dept Psychiat, New Haven, CT 06510 USA
[3] Johns Hopkins Univ, Sch Med, Dept Psychiat, Baltimore, MD 21201 USA
关键词
Huntington's disease; implicit learning; serial reaction time; functional MRI; striatum;
D O I
10.1016/j.pscychresns.2004.03.002
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
The aim of this study was to investigate pathophysiological changes at an early stage of clinical Huntington's disease (HD) using a functional magnetic resonance imaging (fMRI) study and a serial reaction time task paradigm. Mildly affected and presymptomatic HD subjects (n = 8) and healthy normal controls (NC, n = 12) were studied. A group behavioral effect of implicit learning was seen only in the control population. Individual statistical parametric mapping (SPM) analysis showed more consistent activation of the caudate nucleus and putamen in the NC group. In the HD group, the group average SPM showed significant activation in the right head of caudate nucleus, as well as bilateral thalami, left middle temporal, right superior temporal, right superior frontal, right middle and inferior frontal and right postcentral gyri. In the comparison of between-group differences (NC-HD), reduced activation in the HD group relative to NC was observed in the right middle frontal, left middle occipital, left precuneus, and left middle frontal gyri. The variable striatal activity in the Huntington's group suggests early functional loss possibly associated with previously demonstrated early atrophy of these same neural structures. (C) 2004 Elsevier Ireland Ltd. All rights reserved.
引用
收藏
页码:23 / 30
页数:8
相关论文
共 27 条
[1]  
[Anonymous], P IEEE NUCL SCI S ME
[2]   Inhibition of subliminally primed responses is mediated by the caudate and thalamus: evidence from functional MRI and Huntington's disease [J].
Aron, AR ;
Schlaghecken, F ;
Fletcher, PC ;
Bullmore, ET ;
Eimer, M ;
Barker, R ;
Sahakian, BJ ;
Robbins, TW .
BRAIN, 2003, 126 :713-723
[3]   Basal ganglia volume and proximity to onset in presymptomatic Huntington disease [J].
Aylward, EH ;
Codori, AM ;
Barta, PE ;
Pearlson, GD ;
Harris, GJ ;
Brandt, J .
ARCHIVES OF NEUROLOGY, 1996, 53 (12) :1293-1296
[4]   REDUCED BASAL GANGLIA VOLUME ASSOCIATED WITH THE GENE FOR HUNTINGTONS-DISEASE IN ASYMPTOMATIC AT-RISK PERSONS [J].
AYLWARD, EH ;
BRANDT, J ;
CODORI, AM ;
MANGUS, RS ;
BARTA, PE ;
HARRIS, GJ .
NEUROLOGY, 1994, 44 (05) :823-828
[5]   Dissociation between intentional and incidental sequence learning in Huntington's disease [J].
Brown, RG ;
Redondo-Verge, L ;
Chacon, JR ;
Lucas, ML ;
Channon, S .
BRAIN, 2001, 124 :2188-2202
[6]   Altered functional MRI responses in Huntington's disease [J].
Clark, VP ;
Lai, S ;
Deckel, AW .
NEUROREPORT, 2002, 13 (05) :703-706
[7]  
Curran T., 1995, PSYCHE, V2
[8]   Role of the striatum, cerebellum, and frontal lobes in the learning of a visuomotor sequence [J].
Doyon, J ;
Gaudreau, D ;
Laforce, R ;
Castonguay, M ;
Bedard, PJ ;
Bedard, F ;
Bouchard, JP .
BRAIN AND COGNITION, 1997, 34 (02) :218-245
[9]   Functional anatomy of visuomotor skill learning in human subjects examined with positron emission tomography [J].
Doyon, J ;
Owen, AM ;
Petrides, M ;
Sziklas, V ;
Evans, AC .
EUROPEAN JOURNAL OF NEUROSCIENCE, 1996, 8 (04) :637-648
[10]  
First M.B., 2007, STRUCTURED CLIN INTE