Temporal order memory deficits prior to clinical diagnosis in Huntington’s disease

2009 ◽  
Vol 15 (5) ◽  
pp. 662-670 ◽  
Author(s):  
EVA PIROGOVSKY ◽  
JODY GOLDSTEIN ◽  
GUERRY PEAVY ◽  
MARK W. JACOBSON ◽  
JODY COREY-BLOOM ◽  
...  

AbstractThe current study examined temporal order memory in preclinical Huntington’s disease (pre-HD). Participants were separated into less than 5 years (pre-HD near) and more than 5 years (pre-HD far) from estimated age of clinical diagnosis. Participants completed a temporal order memory task on a computerized radial eight-arm maze. On the study phase of each trial, participants viewed a random sequence of circles appearing one at a time at the end of each arm. On the choice phase, participants viewed two circles at the end of the study phase arms and chose the circle occurring earliest in the sequence. The task involved manipulations of the temporal lag, defined as the number of arms occurring in the sample phase sequence between the two choice phase arms. Research suggests that there is more interference for temporally proximal stimuli relative to temporally distal stimuli. There were no significant differences between the pre-HD far group and controls on the temporal order memory task. The pre-HD near group demonstrated significant impairments relative to the other groups on closer temporal lags, but were normal on the furthest temporal lag. Therefore, temporal order memory declines with increased temporal interference in pre-HD close to estimated diagnosis of HD. (JINS, 2009, 15, 662–670.)

2013 ◽  
Vol 2 (3) ◽  
pp. 297-304
Author(s):  
Diane R. Nicoll ◽  
Eva Pirogovsky ◽  
Adrienne E. Collazo ◽  
Savanna M. Tierney ◽  
Jody Corey-Bloom ◽  
...  

2018 ◽  
Author(s):  
Maria V. Soloveva ◽  
Sharna D. Jamadar ◽  
Dennis Velakoulis ◽  
Govinda Poudel ◽  
Nellie Georgiou Karistianis

AbstractPresymptomatic Huntington’s disease (pre-HD) individuals tend to increase functional brain activity to compensate for HD-related brain anomalies. We used a quantitative model of compensation, known as the CRUNCH (Compensation-Related Utilization of Neural Circuits Hypothesis) to explicitly characterise compensation in pre-HD. We acquired functionalmagnetic resonance imaging (fMRI) data (n = 15 pre-HD; n = 15 controls) during performance of an 18-minute fMRI visuospatial working memory task with low, intermediate-1, intermediate-2, and high memory loads. Consistent with the CRUNCH prediction, pre-HD individuals showed decreased fMRI activity in left intraparietal sulcus at high memory load, compared to healthy controls who showed increased fMRI activity in left intraparietal sulcus at high memory load. Contrary to the other CRUNCH prediction, the pre-HD group did not show compensatory increase in fMRI activity at lower levels of memory loads in left intraparietal sulcus. Our findings provide partial support for the validity of CRUNCH in pre-HD.HighlightsVisuospatial working memory deficits in pre-HD occur 25 years prior to predicted disease onsetTask demands differentially affect fMRI activity in left intraparietal sulcusCRUNCH can partially apply in Huntington’s disease


2018 ◽  
Vol 83 (3) ◽  
pp. 532-543 ◽  
Author(s):  
Sarah L. Mason ◽  
Richard E. Daws ◽  
Eyal Soreq ◽  
Eileanoir B. Johnson ◽  
Rachael I. Scahill ◽  
...  

2017 ◽  
Vol 23 (2) ◽  
pp. 159-170 ◽  
Author(s):  
Maria B. Misiura ◽  
Spencer Lourens ◽  
Vince D. Calhoun ◽  
Jeffrey Long ◽  
Jeremy Bockholt ◽  
...  

AbstractObjectives:Huntington’s disease (HD) is a debilitating genetic disorder characterized by motor, cognitive and psychiatric abnormalities associated with neuropathological decline. HD pathology is the result of an extended chain of CAG (cytosine, adenine, guanine) trinucleotide repetitions in theHTTgene. Clinical diagnosis of HD requires the presence of an otherwise unexplained extrapyramidal movement disorder in a participant at risk for HD. Over the past 15 years, evidence has shown that cognitive, psychiatric, and subtle motor dysfunction is evident decades before traditional motor diagnosis. This study examines the relationships among subcortical brain volumes and measures of emerging disease phenotype in prodromal HD, before clinical diagnosis.Methods:The dataset includes 34 cognitive, motor, psychiatric, and functional variables and five subcortical brain volumes from 984 prodromal HD individuals enrolled in the PREDICT HD study. Using cluster analyses, seven distinct clusters encompassing cognitive, motor, psychiatric, and functional domains were identified. Individual cluster scores were then regressed against the subcortical brain volumetric measurements.Results:Accounting for site and genetic burden (the interaction of age and CAG repeat length) smaller caudate and putamen volumes were related to clusters reflecting motor symptom severity, cognitive control, and verbal learning.Conclusions:Variable reduction of the HD phenotype using cluster analysis revealed biologically related domains of HD and are suitable for future research with this population. Our cognitive control cluster scores show sensitivity to changes in basal ganglia both within and outside the striatum that may not be captured by examining only motor scores. (JINS, 2017,23, 159–170)


1994 ◽  
Vol 57 (10) ◽  
pp. 1277-1277 ◽  
Author(s):  
J Warner ◽  
L Barron ◽  
D St Clair ◽  
D Brock

2017 ◽  
Vol 114 (51) ◽  
pp. 13555-13560 ◽  
Author(s):  
Yuji Naya ◽  
He Chen ◽  
Cen Yang ◽  
Wendy A. Suzuki

Neuropsychological and neurophysiological studies have emphasized the role of the prefrontal cortex (PFC) in maintaining information about the temporal order of events or items for upcoming actions. However, the medial temporal lobe (MTL) has also been considered critical to bind individual events or items to their temporal context in episodic memory. Here we characterize the contributions of these brain areas by comparing single-unit activity in the dorsal and ventral regions of macaque lateral PFC (d-PFC and v-PFC) with activity in MTL areas including the hippocampus (HPC), entorhinal cortex, and perirhinal cortex (PRC) as well as in area TE during the encoding phase of a temporal-order memory task. The v-PFC cells signaled specific items at particular time periods of the task. By contrast, MTL cortical cells signaled specific items across multiple time periods and discriminated the items between time periods by modulating their firing rates. Analysis of the temporal dynamics of these signals showed that the conjunctive signal of item and temporal-order information in PRC developed earlier than that seen in v-PFC. During the delay interval between the two cue stimuli, while v-PFC provided prominent stimulus-selective delay activity, MTL areas did not. Both regions of PFC and HPC exhibited an incremental timing signal that appeared to represent the continuous passage of time during the encoding phase. However, the incremental timing signal in HPC was more prominent than that observed in PFC. These results suggest that PFC and MTL contribute to the encoding of the integration of item and timing information in distinct ways.


The Lancet ◽  
1987 ◽  
Vol 330 (8567) ◽  
pp. 1088-1089 ◽  
Author(s):  
J. Hammer ◽  
M. Mächler ◽  
W. Schmid ◽  
M. Schomig-Spingler

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