Double-blind crossover study of branched-chain amino acid therapy in patients with spinocerebellar degeneration

被引:31
作者
Mori, M [1 ]
Adachi, Y [1 ]
Mori, N [1 ]
Kurihara, S [1 ]
Kashiwaya, Y [1 ]
Kusumi, M [1 ]
Takeshima, T [1 ]
Nakashima, K [1 ]
机构
[1] Tottori Univ, Fac Med, Inst Neurol Sci, Div Neurol, Yonago, Tottori 6838504, Japan
关键词
international cooperative ataxia rating scale; BCAA; cerebellar ataxia; SCD; SCA6;
D O I
10.1016/S0022-510X(02)00009-6
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
To determine whether treatment with branched-chain amino acids (BCAA) can improve the condition of patients with ataxia, a double-blind crossover study of BCAA therapy was performed in 16 patients with spinocerebellar degeneration (SCD). The patients were treated with BCAA in oral doses of 1.5, 3.0, or 6.0 g or with placebo daily for 4 weeks in each study phase. The order of treatment phases (placebo or BCAA) was assigned randomly. An International Cooperative Ataxia Rating Scale (ICARS) was used to quantify the severity of symptoms of SCD. The mean ICARS score improved significantly with BCAA treatment compared with the mean pretreatment score (p<0.01). In addition, the improvement in the mean global ICARS score was significant in the middle-dose group compared with that in the placebo group (p<0.02). The estimated improvement in kinetic functions compared with pretreatment (p<0.01) was significant after treatment with BCAA, 1.5 and 3.0 g. All of the responders manifested predominantly cerebellar symptoms, especially those with spinocerebellar ataxia type 6 (SCA6). Thus, treatment with BCAA may be effective in patients with the cerebellar form of SCD. (C) 2002 Elsevier Science B.V. All rights reserved.
引用
收藏
页码:149 / 152
页数:4
相关论文
共 14 条
[1]   SPINOCEREBELLAR DEGENERATIONS IN JAPAN - A NATIONWIDE EPIDEMIOLOGIC AND CLINICAL-STUDY [J].
HIRAYAMA, K ;
TAKAYANAGI, T ;
NAKAMURA, R ;
YANAGISAWA, N ;
HATTORI, T ;
KITA, K ;
YANAGIMOTO, S ;
FUJITA, M ;
NAGAOKA, M ;
SATOMURA, Y ;
SOBUE, I ;
IIZUKA, R ;
TOYOKURA, Y ;
SATOYOSHI, E .
ACTA NEUROLOGICA SCANDINAVICA, 1994, 89 :1-22
[2]   Clinical, neuropathological, and molecular study in two families with spinocerebellar ataxia type 6 (SCA6) [J].
Ishikawa, K ;
Watanabe, M ;
Yoshizawa, K ;
Fujita, T ;
Iwamoto, H ;
Yoshizawa, T ;
Harada, K ;
Nakamagoe, K ;
Komatsuzaki, Y ;
Satoh, A ;
Doi, M ;
Ogata, T ;
Kanazawa, I ;
Shoji, S ;
Mizusawa, H .
JOURNAL OF NEUROLOGY NEUROSURGERY AND PSYCHIATRY, 1999, 67 (01) :86-89
[3]   Molecular features of the CAG repeats of spinocerebellar ataxia 6 (SCA6) [J].
Matsuyama, Z ;
Kawakami, H ;
Maruyama, H ;
Izumi, Y ;
Komure, O ;
Udaka, F ;
Kameyama, M ;
Nishio, T ;
Kuroda, Y ;
Nishimura, M ;
Nakamura, S .
HUMAN MOLECULAR GENETICS, 1997, 6 (08) :1283-1287
[4]   A genetic epidemiological study of spinocerebellar ataxias in Tottori Prefecture, Japan [J].
Mori, M ;
Adachi, Y ;
Kusumi, M ;
Nakashima, K .
NEUROEPIDEMIOLOGY, 2001, 20 (02) :144-149
[5]   Spinocerebellar ataxia type 6: founder effect in western Japan [J].
Mori, M ;
Adachi, Y ;
Kusumi, M ;
Nakashima, K .
JOURNAL OF THE NEUROLOGICAL SCIENCES, 2001, 185 (01) :43-47
[6]   Branched-chain amino acid therapy for spinocerebellar degeneration: A pilot clinical crossover trial [J].
Mori, N ;
Adachi, Y ;
Takeshima, T ;
Kashiwaya, Y ;
Okada, A ;
Nakashima, K .
INTERNAL MEDICINE, 1999, 38 (05) :401-406
[7]  
MORI N, 1998, TRIAL AMINO ACID THE, P48
[8]  
MORI N, 2000, J YONAGO MED ASSOC, V51, P72
[9]   PLASMA-LEVELS OF AMINO-ACIDS CORRELATE WITH MOTOR FLUCTUATIONS IN PARKINSONISM [J].
PINCUS, JH ;
BARRY, KM .
ARCHIVES OF NEUROLOGY, 1987, 44 (10) :1006-1009
[10]   Close associations between prevalences of dominantly inherited spinocerebellar ataxias with CAG-repeat expansions and frequencies of large normal CAG alleles in Japanese and Caucasian populations [J].
Takano, H ;
Cancel, G ;
Ikeuchi, T ;
Lorenzetti, D ;
Mawad, R ;
Stevanin, G ;
Didierjean, O ;
Durr, A ;
Oyake, M ;
Shimohata, T ;
Sasaki, R ;
Koide, R ;
Igarashi, S ;
Hayashi, S ;
Takiyama, Y ;
Nishizawa, M ;
Tanaka, H ;
Zoghbi, H ;
Brice, A ;
Tsuji, S .
AMERICAN JOURNAL OF HUMAN GENETICS, 1998, 63 (04) :1060-1066