Literature DB >> 21094653

Visuomotor integration deficits precede clinical onset in Huntington's disease.

Miranda J Say1, Rebecca Jones, Rachael I Scahill, Eve M Dumas, Allison Coleman, Rachelle C Dar Santos, Damian Justo, J Colin Campbell, Sarah Queller, E Arthur Shores, Sarah J Tabrizi, Julie C Stout.   

Abstract

OBJECTIVES: Visuomotor integration deficits have been documented in Huntington disease (HD), with disproportionately more impairment when direct visual feedback is unavailable. Visuomotor integration under direct and indirect visual feedback conditions has not been investigated in the stage before clinical onset ('premanifest'). However, given evidence of posterior cortical atrophy in premanifest HD, we predicted visuomotor integration would be adversely affected, with greater impairment under conditions of indirect visual feedback.
METHODS: 239 subjects with the HD CAG expansion, ranging from more than a decade before predicted clinical onset until early stage disease, and 122 controls, completed a circle-tracing task, which included both direct and indirect visual feedback conditions. Measures included accuracy, speed, and speed of error detection and correction. Using brain images acquired with 3T magnetic resonance imaging (MRI), we generated grey and white matter volumes with voxel-based morphometry, and analyzed correlations with circle-tracing performance.
RESULTS: Compared with controls, early HD was associated with lower accuracy and slower performance in both circle-tracing conditions. Premanifest HD was associated with lower accuracy in both conditions and fewer rotations in the direct condition. Comparing performance in the indirect condition with the direct condition, HD gene expansion-carriers exhibited a disproportionate increase in errors relative to controls. Premanifest and early HD groups required longer to detect and correct errors, especially in the indirect condition. Slower performance in the indirect condition was associated with lower grey matter volumes in the left somatosensory cortex in VBM analyses.
CONCLUSIONS: Visuomotor integration deficits are evident many years before the clinical onset of HD, with deficits in speed, accuracy, and speed of error detection and correction. The visuomotor transformation demands of the indirect condition result in a disproportionate decrease in accuracy in the HD groups. Slower performance under indirect visual feedback was associated with atrophy of the left-hemisphere somatosensory cortex, which may reflect the proprioceptive demands of the task. Copyright Â
© 2010 Elsevier Ltd. All rights reserved.

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Year:  2010        PMID: 21094653     DOI: 10.1016/j.neuropsychologia.2010.11.016

Source DB:  PubMed          Journal:  Neuropsychologia        ISSN: 0028-3932            Impact factor:   3.139


  19 in total

1.  Regional atrophy associated with cognitive and motor function in prodromal Huntington disease.

Authors:  Elizabeth H Aylward; Deborah L Harrington; James A Mills; Peggy C Nopoulos; Christopher A Ross; Jeffrey D Long; Dawei Liu; Holly K Westervelt; Jane S Paulsen
Journal:  J Huntingtons Dis       Date:  2013

Review 2.  Cognitive impairment in Huntington disease: diagnosis and treatment.

Authors:  Jane S Paulsen
Journal:  Curr Neurol Neurosci Rep       Date:  2011-10       Impact factor: 5.081

3.  Effects of task difficulty during dual-task circle tracing in Huntington's disease.

Authors:  Eleftheria Vaportzis; Nellie Georgiou-Karistianis; Andrew Churchyard; Julie C Stout
Journal:  J Neurol       Date:  2014-11-05       Impact factor: 4.849

4.  Cross-sectional and longitudinal multimodal structural imaging in prodromal Huntington's disease.

Authors:  Deborah L Harrington; Jeffrey D Long; Sally Durgerian; Lyla Mourany; Katherine Koenig; Aaron Bonner-Jackson; Jane S Paulsen; Stephen M Rao
Journal:  Mov Disord       Date:  2016-09-13       Impact factor: 10.338

5.  Functional connectivity of primary motor cortex is dependent on genetic burden in prodromal Huntington disease.

Authors:  Katherine A Koenig; Mark J Lowe; Deborah L Harrington; Jian Lin; Sally Durgerian; Lyla Mourany; Jane S Paulsen; Stephen M Rao
Journal:  Brain Connect       Date:  2014-09

6.  Cognitive domains that predict time to diagnosis in prodromal Huntington disease.

Authors:  Deborah Lynn Harrington; Megan M Smith; Ying Zhang; Noelle E Carlozzi; Jane S Paulsen
Journal:  J Neurol Neurosurg Psychiatry       Date:  2012-03-26       Impact factor: 10.154

7.  Apathy Associated With Impaired Recognition of Happy Facial Expressions in Huntington's Disease.

Authors:  Katherine Osborne-Crowley; Sophie C Andrews; Izelle Labuschagne; Akshay Nair; Rachael Scahill; David Craufurd; Sarah J Tabrizi; Julie C Stout
Journal:  J Int Neuropsychol Soc       Date:  2019-02-15       Impact factor: 2.892

8.  Network topology and functional connectivity disturbances precede the onset of Huntington's disease.

Authors:  Deborah L Harrington; Mikail Rubinov; Sally Durgerian; Lyla Mourany; Christine Reece; Katherine Koenig; Ed Bullmore; Jeffrey D Long; Jane S Paulsen; Stephen M Rao
Journal:  Brain       Date:  2015-06-09       Impact factor: 13.501

9.  Neuroanatomical correlates of cognitive functioning in prodromal Huntington disease.

Authors:  Deborah L Harrington; Dawei Liu; Megan M Smith; James A Mills; Jeffrey D Long; Elizabeth H Aylward; Jane S Paulsen
Journal:  Brain Behav       Date:  2013-11-13       Impact factor: 2.708

10.  Characterising Upper Limb Movements in Huntington's Disease and the Impact of Restricted Visual Cues.

Authors:  Jessica Despard; Anne-Marie Ternes; Bleydy Dimech-Betancourt; Govinda Poudel; Andrew Churchyard; Nellie Georgiou-Karistianis
Journal:  PLoS One       Date:  2015-08-06       Impact factor: 3.240

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