Microstructural white matter changes in carriers of the DYT1 gene mutation

Ann Neurol. 2004 Aug;56(2):283-6. doi: 10.1002/ana.20177.

Abstract

We tested the hypothesis that the DYT1 genotype is associated with a disorder of anatomical connectivity involving primarily the sensorimotor cortex. We used diffusion tensor magnetic resonance imaging (DTI) to assess the microstructure of white matter pathways in mutation carriers and control subjects. Fractional anisotropy (FA), a measure of axonal integrity and coherence, was reduced (p < 0.005) in the subgyral white matter of the sensorimotor cortex of DYT1 carriers. Abnormal anatomical connectivity of the supplementary motor area may contribute to the susceptibility of DYT1 carriers to develop clinical manifestations of dystonia.

Publication types

  • Comparative Study
  • Research Support, Non-U.S. Gov't
  • Research Support, U.S. Gov't, P.H.S.

MeSH terms

  • Adult
  • Case-Control Studies
  • Cerebral Cortex / pathology*
  • Cerebral Cortex / physiopathology
  • Diffusion Magnetic Resonance Imaging / methods
  • Dystonia / genetics
  • Dystonia / pathology*
  • Dystonia / physiopathology
  • Female
  • Genetic Predisposition to Disease*
  • Humans
  • Male
  • Middle Aged
  • Molecular Chaperones / genetics*
  • Mutation*

Substances

  • Molecular Chaperones
  • TOR1A protein, human