Cortical excitability in Duchenne muscular dystrophy

Clin Neurophysiol. 2008 Feb;119(2):459-65. doi: 10.1016/j.clinph.2007.09.125. Epub 2007 Nov 28.

Abstract

Objective: To investigate the probable cortical excitability changes in DMD by electrophysiological means.

Methods: Sixteen cases with DMD, 10 age-matched control children (CC) and 10 healthy adult volunteers (AC) were studied with a transcranial magnetic stimulation (TMS) test battery composed of central conduction time, cortical silent period and paired TMS paradigm.

Results: There were no significant differences between DMD and CC groups except for lower amplitude motor responses in DMD cases. These two groups showed a similar pattern of excitability with less short interval intracortical inhibitions and shorter silent period durations as compared to the AC subjects.

Conclusions: The electrophysiological tests performed in our DMD patients did not reveal abnormalities caused particularly by the disorder.

Significance: TMS excitability studies performed in DMD boys may not provide findings other than those related to the developmental age.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adolescent
  • Adult
  • Cerebral Cortex / physiopathology*
  • Child
  • Differential Threshold / physiology
  • Electric Stimulation / methods
  • Evoked Potentials, Motor / physiology*
  • Humans
  • Male
  • Muscular Dystrophy, Duchenne / pathology*
  • Muscular Dystrophy, Duchenne / physiopathology*
  • Neural Conduction
  • Neural Inhibition / physiology
  • Reaction Time / physiology
  • Time Factors
  • Transcranial Magnetic Stimulation / methods