Literature DB >> 9918350

Dystonia in Huntington's disease: prevalence and clinical characteristics.

E D Louis1, P Lee, L Quinn, K Marder.   

Abstract

BACKGROUND: The prevalence and clinical characteristics of dystonia in Huntington's disease (HD) have not been formally assessed.
OBJECTIVES: To study (1) the prevalence of dystonia in HD in a clinic population, (2) the clinical features of dystonia, and (3) clinical correlates of dystonia (for example, age, disease duration).
METHODS: Patients with HD attending the HD Center at the New York State Psychiatric Center were administered the Unified HD Rating Scale and underwent a standardized 5.5-minute videotaped examination. Two neurologists reviewed the videotaped examination and rated the severity and constancy of dystonia, calculating a total dystonia score for each patient.
RESULTS: Prevalence of dystonia of any severity was 95.2%. Twenty-four of 42 (57.1%) had dystonia in at least one body region that was moderate and present more than half of the time, and seven of 42 (16.7%) had dystonia that was severe and constant. The most prevalent types of dystonia were internal shoulder rotation (64.3%), sustained fist clenching (47.1%), excessive knee flexion (42.9%), and foot inversion (42.9%). In 37 of 42 (88.1%) patients, there were more than two types of dystonia, and in the average patient, three to four types of dystonia. The mean severity was between 1 (mild) and 2 (moderate), and the mean constancy was between 2 (present less than half of the time) and 3 (present more than half of the time). Multivariate linear regression revealed that disease duration (p = 0.0005) and taking an antidopaminergic agent (p = 0.03) were positively associated with the total dystonia score.
CONCLUSIONS: The majority of patients in this HD clinic exhibited some dystonia. The dystonia was present in several body regions and manifested by a variety of movements and postures not typical of idiopathic torsion dystonia. The dystonia was not bothersome to most patients, and its severity was a function of disease duration and use of an antidopaminergic agent.

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Year:  1999        PMID: 9918350     DOI: 10.1002/1531-8257(199901)14:1<95::aid-mds1016>3.0.co;2-8

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


  12 in total

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Authors:  Valerie B Thompson; H A Jinnah; Ellen J Hess
Journal:  Expert Opin Ther Targets       Date:  2011-12-03       Impact factor: 6.902

Review 2.  The functional neuroanatomy of dystonia.

Authors:  Vladimir K Neychev; Robert E Gross; Stephane Lehéricy; Ellen J Hess; H A Jinnah
Journal:  Neurobiol Dis       Date:  2011-02-12       Impact factor: 5.996

3.  Huntington's Disease Revealed by Familial Cervical Dystonia.

Authors:  Daniela Andriuta; Mélissa Tir; Olivier Godefroy; Pierre Krystkowiak
Journal:  Mov Disord Clin Pract       Date:  2016-01-18

Review 4.  The neurobiological basis for novel experimental therapeutics in dystonia.

Authors:  Anthony M Downs; Kaitlyn M Roman; Simone A Campbell; Antonio Pisani; Ellen J Hess; Paola Bonsi
Journal:  Neurobiol Dis       Date:  2019-07-04       Impact factor: 5.996

5.  Gedunin Degrades Aggregates of Mutant Huntingtin Protein and Intranuclear Inclusions via the Proteasomal Pathway in Neurons and Fibroblasts from Patients with Huntington's Disease.

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6.  Striatal parvalbuminergic neurons are lost in Huntington's disease: implications for dystonia.

Authors:  Anton Reiner; Evan Shelby; Hongbing Wang; Zena Demarch; Yunping Deng; Natalie Hart Guley; Virginia Hogg; Richard Roxburgh; Lynette J Tippett; Henry J Waldvogel; Richard L M Faull
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Review 7.  Risk-taking and pathological gambling behavior in Huntington's disease.

Authors:  Carla Kalkhoven; Cor Sennef; Ard Peeters; Ruud van den Bos
Journal:  Front Behav Neurosci       Date:  2014-04-02       Impact factor: 3.558

8.  Cause or effect: Altered brain and network activity in cervical dystonia is partially normalized by botulinum toxin treatment.

Authors:  Stefan Brodoehl; Franziska Wagner; Tino Prell; Carsten Klingner; O W Witte; Albrecht Günther
Journal:  Neuroimage Clin       Date:  2019-03-26       Impact factor: 4.881

9.  Motor onset and diagnosis in Huntington disease using the diagnostic confidence level.

Authors:  Dawei Liu; Jeffrey D Long; Ying Zhang; Lynn A Raymond; Karen Marder; Anne Rosser; Elizabeth A McCusker; James A Mills; Jane S Paulsen
Journal:  J Neurol       Date:  2015-09-26       Impact factor: 4.849

10.  The Prevalence of Juvenile Huntington's Disease: A Review of the Literature and Meta-Analysis.

Authors:  Oliver Quarrell; Kirsty L O'Donovan; Oliver Bandmann; Mark Strong
Journal:  PLoS Curr       Date:  2012-07-20
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