Bonnet A M, Esteguy M, Tell G, Schechter P J, Hardenberg J, Agid Y
Can J Neurol Sci. 1986 Nov;13(4):331-3. doi: 10.1017/s0317167100036672.
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.
在一项双盲、安慰剂对照的交叉研究中,对14例小脑共济失调患者(9例弗里德赖希共济失调患者,5例橄榄脑桥小脑萎缩患者)口服给予每日剂量为2 - 4克的氨己烯酸(γ-乙烯基氨基丁酸;GVG),一种γ-氨基丁酸转氨酶的不可逆抑制剂,以及安慰剂,各用药4个月。对于整个组而言,在测量的任何小脑症状学参数方面,氨己烯酸组和安慰剂组之间没有显著差异。个别来看,一名患者在接受每日2克氨己烯酸治疗3个月后显示出一些改善。对每日4克氨己烯酸的耐受性较差,而每日2克耐受性良好。结果表明,增加中枢γ-氨基丁酸浓度的药物不太可能对弗里德赖希共济失调或橄榄脑桥小脑萎缩患者有益。