Literature DB >> 20818666

Impaired postural stability as a marker of premanifest Huntington's disease.

Danielle Salomonczyk1, Robert Panzera, Eva Pirogovosky, Jody Goldstein, Jody Corey-Bloom, Roger Simmons, Paul E Gilbert.   

Abstract

Subtle changes in fine motor control have been observed in individuals who carry the Huntington's disease (HD) mutation but have not yet manifested symptoms, referred to as premanifest HD (preHD). However, few studies have examined gross motor impairments in this population. This study sought to examine the role of sensory involvement in maintaining postural stability during the premanifest and manifest stages of HD using computerized dynamic posturography. Eleven HD participants, 22 preHD subdivided into "preHD Near" (<5 years from estimated clinical onset) and "preHD Far" (>5 years from estimated clinical onset), and 17 nongene carriers (NGC) completed a sensory organization test (SOT) to assess postural control when vestibular, visual, and somatosensory information was systematically degraded. The HD group demonstrated greater postural sway than the NGC and preHD Far groups on all conditions including baseline, and greater postural sway than the preHD Near group when sensory information was manipulated. The preHD Near group showed significantly greater postural sway than the preHD Far group when visual and somatosensory information was degraded and only vestibular information was available and reliable for maintaining postural stability. The results of this study highlight subtle postural deficits in the face of changing sensory conditions in preHD up to 5 years before estimated disease onset. The findings suggest that the SOT may be a highly sensitive indicator of early motor impairment and subsequent phenoconversion to manifest HD in preHD.

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Year:  2010        PMID: 20818666     DOI: 10.1002/mds.23309

Source DB:  PubMed          Journal:  Mov Disord        ISSN: 0885-3185            Impact factor:   10.338


  8 in total

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Review 2.  Comprehensive neurocognitive endophenotyping strategies for mouse models of genetic disorders.

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4.  Characterization and Early Detection of Balance Deficits in Fragile X Premutation Carriers With and Without Fragile X-Associated Tremor/Ataxia Syndrome (FXTAS).

Authors:  Joan A O'Keefe; Erin Robertson-Dick; Emily J Dunn; Yan Li; Youping Deng; Amber N Fiutko; Elizabeth Berry-Kravis; Deborah A Hall
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5.  The Effects of Dual-Task Cognitive Interference and Environmental Challenges on Balance in Huntington's Disease.

Authors:  Nicollette L Purcell; Jennifer G Goldman; Bichun Ouyang; Bryan Bernard; Joan A O'Keefe
Journal:  Mov Disord Clin Pract       Date:  2019-01-16

6.  Clinical assessment of the effect of tetrabenazine on functional scales in huntington disease: a pilot open label study.

Authors:  Robert Fekete; Anthony Davidson; Joseph Jankovic
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7.  Computerised Dynamic Posturography in Premanifest and Manifest individuals with Huntington's Disease.

Authors:  Alvaro Reyes; Danielle Salomonczyk; Wei-Peng Teo; Luis D Medina; Danielle Bartlett; Eva Pirogovsky-Turk; Pauline Zaenker; Jody Corey Bloom; Roger W Simmons; Mel Ziman; Paul E Gilbert; Travis Cruickshank
Journal:  Sci Rep       Date:  2018-10-02       Impact factor: 4.379

8.  Dual tasking impairments are associated with striatal pathology in Huntington's disease.

Authors:  Johnny Lo; Alvaro Reyes; Timothy S Pulverenti; Timothy J Rankin; Danielle M Bartlett; Pauline Zaenker; Grant Rowe; Kirk Feindel; Govinda Poudel; Nellie Georgiou-Karistianis; Mel R Ziman; Travis M Cruickshank
Journal:  Ann Clin Transl Neurol       Date:  2020-08-14       Impact factor: 4.511

  8 in total

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