Literature DB >> 26708559

Pattern of Peripheral Nerve Involvement in Spinocerebellar Ataxia Type 2: a Neurophysiological Assessment.

Marcio Luiz Escorcio Bezerra1, José Luiz Pedroso2, Pedro Braga-Neto1,3, Agessandro Abrahao1, Marcus Vinicius Cristino de Albuquerque1, Franklin Roberto Pereira Borges4,5, Maria Luiza Saraiva-Pereira6, Laura Bannach Jardim7, Nadia Iandoli de Oliveira Braga1, Gilberto Mastrocola Manzano1, Orlando G P Barsottini1.   

Abstract

Peripheral neuropathy is frequent in spinocerebellar ataxia type 2 (SCA2), but the pattern and characteristics of nerve involvement are still an unsettled issue. This study aimed to evaluate the prevalence, extent, and distribution of nerve involvement in SCA2 patients through neurophysiological studies. Thirty-one SCA2 patients and 20 control subjects were enrolled in this study. All subjects were prospectively evaluated through electromyography, including nerve conduction, needle electromyography in proximal and distal muscles of the upper and lower limbs, and sural radial amplitude ratio (SRAR). We aimed to differentiate distal axonopathy from diffuse nerve commitment, characterizing neuronopathy. Nerve involvement was observed in 83.6 % (26 individuals) of SCA2 patients. Among these, 19 had diffuse sensory abnormalities on nerve conduction predominantly on the upper limbs, with diffuse chronic denervation on needle electromyography and elevated SRAR values. Four individuals had only diffuse sensory involvement, and 2 had only motor involvement on needle evaluation and normal nerve conduction. These were interpreted as neuronopathy due to the diffuse distribution of the involvement. One individual had distal sensory axonopathy, with lower limb predominance. In this study, we found neuronopathy as the main pattern of nerve involvement in SCA2 patients and that motor involvement is a frequent feature. This information brings new insights into the understanding of the pathophysiology of nerve involvement in SCA2 and sets some key points about the phenotype, which is relevant to guide the genetic/molecular diagnosis.

Entities:  

Keywords:  Neuronopathy; Peripheral neuropathy; SCA2; Spinocerebellar ataxia type 2; Spinocerebellar ataxias

Mesh:

Year:  2016        PMID: 26708559     DOI: 10.1007/s12311-015-0753-x

Source DB:  PubMed          Journal:  Cerebellum        ISSN: 1473-4222            Impact factor:   3.847


  30 in total

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Authors:  João Antonio Maciel Nobrega; Denise Spinola Pinheiro; Gilberto Mastrocola Manzano; Jun Kimura
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Review 2.  Distal symmetric polyneuropathy: a definition for clinical research: report of the American Academy of Neurology, the American Association of Electrodiagnostic Medicine, and the American Academy of Physical Medicine and Rehabilitation.

Authors:  J D England; G S Gronseth; G Franklin; R G Miller; A K Asbury; G T Carter; J A Cohen; M A Fisher; J F Howard; L J Kinsella; N Latov; R A Lewis; P A Low; A J Sumner
Journal:  Neurology       Date:  2005-01-25       Impact factor: 9.910

3.  Electrophysiological evaluation of spinocerebellar ataxias 1, 2 and 3.

Authors:  Ravi Yadav; Pramod Kumar Pal; Nithin Krishna; B R Amar; Sanjeev Jain; Meera Purushottam
Journal:  J Neurol Sci       Date:  2011-08-31       Impact factor: 3.181

Review 4.  The neuropathology of CAG repeat diseases: review and update of genetic and molecular features.

Authors:  Y Robitaille; I Lopes-Cendes; M Becher; G Rouleau; A W Clark
Journal:  Brain Pathol       Date:  1997-07       Impact factor: 6.508

5.  FTLD-ALS of TDP-43 type and SCA2 in a family with a full ataxin-2 polyglutamine expansion.

Authors:  Dirk Bäumer; Simon Z East; Bing Tseu; Adam Zeman; David Hilton; Kevin Talbot; Olaf Ansorge
Journal:  Acta Neuropathol       Date:  2014-04-10       Impact factor: 17.088

6.  Expression of ataxin-2 in brains from normal individuals and patients with Alzheimer's disease and spinocerebellar ataxia 2.

Authors:  D P Huynh; M R Del Bigio; D H Ho; S M Pulst
Journal:  Ann Neurol       Date:  1999-02       Impact factor: 10.422

7.  Machado-Joseph disease presenting as motor neuron disease.

Authors:  Susana Pinto; Mamede De Carvalho
Journal:  Amyotroph Lateral Scler       Date:  2008-06

8.  Electrophysiological features in patients and presymptomatic relatives with spinocerebellar ataxia type 2.

Authors:  Luis Velázquez Pérez; Gilberto Sánchez Cruz; Nalia Canales Ochoa; Roberto Rodríguez Labrada; Julio Rodríguez Díaz; Luis Almaguer Mederos; José Laffita Mesa
Journal:  J Neurol Sci       Date:  2007-08-13       Impact factor: 3.181

9.  Prospective study of peripheral neuropathy in Machado-Joseph disease.

Authors:  Marcondes C França; Anelyssa D'abreu; Anamarli Nucci; Fernando Cendes; Iscia Lopes-Cendes
Journal:  Muscle Nerve       Date:  2009-12       Impact factor: 3.217

10.  Spinocerebellar ataxias in Brazil--frequencies and modulating effects of related genes.

Authors:  Raphael Machado de Castilhos; Gabriel Vasata Furtado; Tailise Conte Gheno; Paola Schaeffer; Aline Russo; Orlando Barsottini; José Luiz Pedroso; Diego Z Salarini; Fernando Regla Vargas; Maria Angélica de Faria Domingues de Lima; Clécio Godeiro; Luiz Carlos Santana-da-Silva; Maria Betânia Pereira Toralles; Silvana Santos; Hélio van der Linden; Hector Yuri Wanderley; Paula Frassineti Vanconcelos de Medeiros; Eliana Ternes Pereira; Erlane Ribeiro; Maria Luiza Saraiva-Pereira; Laura Bannach Jardim
Journal:  Cerebellum       Date:  2014-02       Impact factor: 3.847

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  1 in total

Review 1.  The Intersection Between Cerebellar Ataxia and Neuropathy: a Proposed Classification and a Diagnostic Approach.

Authors:  Cristina Saade Jaques; Marcio Luiz Escorcio-Bezerra; José Luiz Pedroso; Orlando Graziani Povoas Barsottini
Journal:  Cerebellum       Date:  2021-08-09       Impact factor: 3.847

  1 in total

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