A controlled study of oral vigabatrin (gamma-vinyl GABA) in patients with cerebellar ataxia

Can J Neurol Sci. 1986 Nov;13(4):331-3. doi: 10.1017/s0317167100036672.

Abstract

Vigabatrin (gamma-vinyl GABA; GVG), an irreversible inhibitor of GABA-transaminase, at a daily dose of 2-4 g, and a placebo were each administered orally for 4 months to 14 patients with cerebellar ataxia (9 with Friedreich's ataxia, 5 with olivopontocerebellar atrophy), in a double-blind, placebo-controlled crossover study. For the group as a whole, there was no significant difference between the GVG and placebo periods in any of the parameters of cerebellar symptomatology measured. Individually, one patient showed some improvement after 3 months of treatment with 2 g/day GVG. Tolerance to 4 g/day GVG was poor, whereas 2 g/day was well tolerated. The results suggest that agents which increase central GABA concentrations are not likely to be of benefit to patients with Friedreich's ataxia or olivopontocerebellar atrophy.

Publication types

  • Clinical Trial
  • Controlled Clinical Trial

MeSH terms

  • Adolescent
  • Adult
  • Aminocaproates / adverse effects
  • Aminocaproates / therapeutic use*
  • Double-Blind Method
  • Drug Evaluation
  • Friedreich Ataxia / drug therapy*
  • Humans
  • Male
  • Middle Aged
  • Neurologic Examination
  • Olivopontocerebellar Atrophies / drug therapy*
  • Random Allocation
  • Spinocerebellar Degenerations / drug therapy*
  • Vigabatrin

Substances

  • Aminocaproates
  • Vigabatrin