Literature DB >> 24781836

Quantitative analysis of upper-limb ataxia in patients with spinocerebellar degeneration.

Naohisa Ueda1, Yasuhito Hakii, Shigeru Koyano, Yuichi Higashiyama, Hideto Joki, Yasuhisa Baba, Yume Suzuki, Yoshiyuki Kuroiwa, Fumiaki Tanaka.   

Abstract

Spinocerebellar degeneration (SCD) is a progressive neurodegenerative disorder in which cerebellar ataxia causes motor disability. There are no widely applicable methods for objective evaluation of ataxia in SCD. An objective system to evaluate ataxia is necessary for use in clinical trials of newly developed medication and rehabilitation. The aim of this study was to develop a simple method to quantify the degree of upper-limb ataxia. Forty-nine patients with SCD participated in this study. Patients were instructed to trace an Archimedean spiral template, and the gap between the template spiral and the drawn spiral (gap area; GA) was measured using Image J software. Ataxia was rated using the Scale for the Assessment and Rating of Ataxia (SARA) and cerebellar volume was evaluated in 37 patients using an axial cross-section of magnetic resonance images that were obtained within 6 months of clinical evaluation. Regression analysis was performed to assess the relation between GA and patient age, disease duration, SARA score, and cerebellar volume. GA was significantly related to total SARA score (r = 0.660, p < 0.001), the posture and gait (r = 0.551, p < 0.001), speech (r = 0.527, p < 0.001), hand movements (r = 0.553, p < 0.001), and heel-shin slide (r = 0.367, p = 0.036) SARA subscores, and cerebellar volume (r = 0.577, p < 0.001) but was not related to patient age (r = 0.176, p = 0.227) or disease duration (r = 0.236, p = 0.103). GA is a simple, useful method to objectively quantify the degree of cerebellar ataxia, especially upper-limb ataxia, and can be widely adopted in various settings, including clinical trials.

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Year:  2014        PMID: 24781836     DOI: 10.1007/s00415-014-7353-4

Source DB:  PubMed          Journal:  J Neurol        ISSN: 0340-5354            Impact factor:   4.849


  27 in total

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4.  Quantitative assessment of brain stem and cerebellar atrophy in spinocerebellar ataxia types 3 and 6: impact on clinical status.

Authors:  L Eichler; B Bellenberg; H K Hahn; O Köster; L Schöls; C Lukas
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6.  Impairments of prehension kinematics and grasping forces in patients with cerebellar degeneration and the relationship to cerebellar atrophy.

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Journal:  Brain       Date:  2008-03-31       Impact factor: 13.501

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9.  Video game-based coordinative training improves ataxia in children with degenerative ataxia.

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10.  Brain structural damage in Friedreich's ataxia.

Authors:  R Della Nave; A Ginestroni; M Giannelli; C Tessa; E Salvatore; F Salvi; M T Dotti; G De Michele; S Piacentini; M Mascalchi
Journal:  J Neurol Neurosurg Psychiatry       Date:  2007-07-18       Impact factor: 10.154

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  1 in total

1.  Quantitative evaluation of upper limb ataxia in spinocerebellar ataxias.

Authors:  Yoshiyuki Kishimoto; Atsushi Hashizume; Yuta Imai; Masahiro Nakatochi; Shinichiro Yamada; Daisuke Ito; Ryota Torii; Yoshitaka Nagano; Hideo Fujimoto; Masahisa Katsuno
Journal:  Ann Clin Transl Neurol       Date:  2022-03-15       Impact factor: 4.511

  1 in total

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