Amantadine in Huntington's disease: open-label video-blinded study

Neurol Sci. 2002 Sep:23 Suppl 2:S83-4. doi: 10.1007/s100720200081.

Abstract

Huntington's disease (HD) is characterized by chorea, cognitive and behavioral changes. Amantadine, a non-competitive NMDA receptor antagonist, has shown an antidyskinetic effect on levodopa-induced dyskinesias, which are known to have strict pathogenetic analogies with choreic hyperkinesias. The antidyskinetic efficacy of amantadine and its effects on cognitive and behavioural symptoms were evaluated. Eight HD patients received oral amantadine (100 mg tid) unblinded for a 1-year period. A significant reduction of dyskinesias was reported ( p<0.01). No changes were observed in neuropsychologic and psychiatric assessments after 6 and 12 months of therapy. These data may have relevance to the treatment of HD with amantadine.

Publication types

  • Clinical Trial

MeSH terms

  • Aged
  • Amantadine / pharmacology*
  • Dyskinesia, Drug-Induced / drug therapy*
  • Dyskinesia, Drug-Induced / metabolism
  • Excitatory Amino Acid Antagonists / pharmacology*
  • Female
  • Humans
  • Huntington Disease / drug therapy*
  • Huntington Disease / metabolism
  • Hyperkinesis / chemically induced
  • Levodopa / adverse effects
  • Male
  • Receptors, N-Methyl-D-Aspartate / metabolism
  • Time Factors

Substances

  • Excitatory Amino Acid Antagonists
  • Receptors, N-Methyl-D-Aspartate
  • Levodopa
  • Amantadine