Task-Set Switching Deficits in Early-Stage Huntington's Disease: Implications for Basal Ganglia Function

2003 ◽  
Vol 15 (5) ◽  
pp. 629-642 ◽  
Author(s):  
Adam R. Aron ◽  
Laura Watkins ◽  
Barbara J. Sahakian ◽  
Stephen Monsell ◽  
Roger A. Barker ◽  
...  

Executive functions are likely mediated by interconnected circuits including frontal lobe and basal ganglia structures. We assessed the executive function of task switching in patients with early-stage Huntington's disease (HD), a neurodegenerative disease affecting the basal ganglia. In two experiments, the HD patients had greater difficulty when switching than when repeating a task than matched controls, and this was true even when scaling for the overall slowing of the patients. In the first experiment, HD patients had a switching deficit even in a “pure” condition where they had to switch, predictably, and with substantial preparation time, between stimuli having only one possible response, indicating a switching deficit different from that for patients with Parkinson's disease or frontal lobe trauma, and possibly relating to inadequate activation of stimulus-response links or “response set.” In the more elaborate second experiment, we could not account for the switching deficit of the patients in terms of inadequate preparation in advance of a switch, deficient suppression of taskset processing from the preswitch trial, or impaired suppression of interference due to the presence of a competing task set. Instead, we found that part of the switching deficit was due to elevated reaction time and errors on switch trials for a repeated response (same button press as on preswitch trial) relative to an alternated response (different button press from preswitch trial). We argue that this elevated “repetition effect” for the HD patients is due to excessive inhibition of the justperformed response in advance of a switch. Alterations in the “response-setting” process alone (Experiment 1) and both the response-setting and “response inhibition” process (Experiment 2) probably arise from striatal pathology in HD, thus accounting for the task-switching deficits and showing how basal ganglia implemented response processes may underpin executive function.

2014 ◽  
Vol 45 (01) ◽  
Author(s):  
C Krogias ◽  
R Hoffmann ◽  
K Straßburger-Krogias ◽  
P Klotz ◽  
G Ellrichmann ◽  
...  

1992 ◽  
Vol 5 (4) ◽  
pp. 205-214 ◽  
Author(s):  
D. H. Jacobs ◽  
S. J. Huber

Neuropsychologic data suggest an important role for the caudate nucleus (CN) in behavioral impairments in Huntington's disease (HD). These include abnormalities in executive function, egocentric visuospatial representations, communication, and retrieval of declarative memories, changes in personality, and psychiatric disturbances. Animal paradigms of CN lesions support a role for the CN in some of these behaviors. Current theories of basal ganglia function add explanatory value to the role of the CN in these behaviors. A disconnection of the caudate from limbic structures, including the amygdala may account for many nonmotor behaviors observed in HD.


2016 ◽  
Vol 33 (S1) ◽  
pp. S371-S371
Author(s):  
S. Mörkl ◽  
C. Blesl ◽  
A. Tmava ◽  
W. Wurm ◽  
A. Holl ◽  
...  

BackgroundHuntington's disease (HD) is characterized by executive dysfunctions like problems with planning, accuracy, inhibition and impulsivity. During the course of the disease executive function worsens with ongoing pathological changes in the basal ganglia. However, it is not clear whether cognitive dysfunction develops gradually or not during the course of the disease.MethodsWe assessed the development of executive dysfunction in 23 patients with early HD and 29 patients with late HD on the Tower of London (ToL) for the number of solved problems, planning time and number of breaks.ResultsHD patients showed a linear decrease of accuracy (as assessed by number of solved problems) during the course of the disease. Controls scored significantly higher than early stage HD patients and early stage HD patients scored significantly higher than late stage HD patients. In planning time and number of breaks a non-linear decrease was found.ConclusionExecutive dysfunctions in HD are not alone connected to degenerative changes in the striatum as they do not develop gradually and linear during the course of the disease. Obviously, executive function could not be seen as a single component, but as a combination of different abilities, which show a non-linear and non-parallel decline.Disclosure of interestThe authors have not supplied their declaration of competing interest.


2014 ◽  
Vol 85 (Suppl 1) ◽  
pp. A46-A46
Author(s):  
C. Saft ◽  
R. Hoffmann ◽  
K. Strassburger-Krogias ◽  
T. Lucke ◽  
S. Meves ◽  
...  

2014 ◽  
Vol 122 (6) ◽  
pp. 825-833 ◽  
Author(s):  
Carsten Saft ◽  
Rainer Hoffmann ◽  
Katrin Strassburger-Krogias ◽  
Thomas Lücke ◽  
Saskia H. Meves ◽  
...  

2015 ◽  
Vol 36 (5) ◽  
pp. 1728-1740 ◽  
Author(s):  
Marianne J.U. Novak ◽  
Kiran K. Seunarine ◽  
Clare R. Gibbard ◽  
Peter McColgan ◽  
Bogdan Draganski ◽  
...  

NeuroImage ◽  
2009 ◽  
Vol 47 ◽  
pp. S115
Author(s):  
R.K. Pierson ◽  
L.J. Beglinger ◽  
V.A. Magnotta ◽  
J. Vaidya ◽  
H. Johnson ◽  
...  

1985 ◽  
Vol 448 (1) ◽  
pp. 488-494 ◽  
Author(s):  
P. C. EMSON ◽  
D. DAWBARN ◽  
M. N. ROSSOR ◽  
J. F. REHFELD ◽  
P. BRUNDIN ◽  
...  

2016 ◽  
Vol 74 (9) ◽  
pp. 761-766 ◽  
Author(s):  
Tiago Attoni ◽  
Rogério Beato ◽  
Serge Pinto ◽  
Francisco Cardoso

ABSTRACT Chorea is an abnormal movement characterized by a continuous flow of random muscle contractions. This phenomenon has several causes, such as infectious and degenerative processes. Chorea results from basal ganglia dysfunction. As the control of the eye movements is related to the basal ganglia, it is expected, therefore, that is altered in diseases related to chorea. Sydenham’s chorea, Huntington’s disease and neuroacanthocytosis are described in this review as basal ganglia illnesses that can present with abnormal eye movements. Ocular changes resulting from dysfunction of the basal ganglia are apparent in saccade tasks, slow pursuit, setting a target and anti-saccade tasks. The purpose of this article is to review the main characteristics of eye motion in these three forms of chorea.


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