Impaired body movement representation in DYT1 mutation carriers

M. Fiorio, M. Gambarin, G. Defazio, E. M. Valente, C. Stanzani, G. Moretto, M. Loi, P. Soliveri, N. Nardocci, A. Albanese, A. Fiaschi, M. Tinazzi

Research output: Contribution to journalArticle

Abstract

Objective: The only known genetic cause of early-onset primary torsion dystonia is the GAG deletion in the DYT1 gene. Due to the reduced penetrance, many mutation carriers remain clinically asymptomatic, despite the presence of subclinical abnormalities, mainly in the motor control circuitry. Our aim was to investigate whether the DYT1 mutation impairs the inner simulation of movements, a fundamental function for motor planning and execution, which relies upon cortical and subcortical systems, dysfunctional in dystonia. Methods: DYT1 manifesting patients, DYT1 non-manifesting carriers and control subjects were asked to fixate body (hand, foot, face) or non-body (car) stimuli on a computer screen. Stimuli were presented at different degrees of orientations and subjects had to mentally rotate them, in order to give a laterality judgement. Reaction times and accuracy were collected. Results: DYT1 carriers, manifesting and non-manifesting dystonic symptoms, were slower in mentally rotating body parts (but not cars) than control subjects. Conclusions: The DYT1 gene mutation is associated with a slowness in mental simulation of movements, independently from the presence of motor symptoms. Significance: These findings suggest that the cognitive representation of body movements may be altered subclinically in dystonia, thus contributing to the endophenotypic trait of disease.

Original languageEnglish
Pages (from-to)1864-1869
Number of pages6
JournalClinical Neurophysiology
Volume119
Issue number8
DOIs
Publication statusPublished - Aug 2008

Keywords

  • Dystonia
  • DYT1 gene
  • Endophenotype
  • Mental rotation
  • Movement representation

ASJC Scopus subject areas

  • Clinical Neurology
  • Radiology Nuclear Medicine and imaging
  • Neurology
  • Sensory Systems
  • Physiology (medical)

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  • Cite this

    Fiorio, M., Gambarin, M., Defazio, G., Valente, E. M., Stanzani, C., Moretto, G., Loi, M., Soliveri, P., Nardocci, N., Albanese, A., Fiaschi, A., & Tinazzi, M. (2008). Impaired body movement representation in DYT1 mutation carriers. Clinical Neurophysiology, 119(8), 1864-1869. https://doi.org/10.1016/j.clinph.2008.04.292