UBIDECARENONE IN THE TREATMENT OF MITOCHONDRIAL MYOPATHIES - A MULTICENTER DOUBLE-BLIND TRIAL

被引:106
作者
BRESOLIN, N
DORIGUZZI, C
PONZETTO, C
ANGELINI, C
MORONI, I
CASTELLI, E
COSSUTTA, E
BINDA, A
GALLANTI, A
GABELLINI, S
PICCOLO, G
MARTINUZZI, A
CIAFALONI, E
ARNAUDO, E
LICIARDELLO, L
CARENZI, A
SCARLATO, G
机构
[1] UNIV TURIN,IST CLIN NEUROL,I-10124 TURIN,ITALY
[2] UNIV PADUA,IST CLIN NEUROL,I-35100 PADUA,ITALY
[3] ZAMBON PHARMACEUT CO,RES LAB,BRESSO,ITALY
[4] UNIV TURIN,DEPT BIOMED SCI ONCOL,I-10124 TURIN,ITALY
[5] UNIV BOLOGNA,INST CLIN NEUROL,I-40126 BOLOGNA,ITALY
[6] UNIV PAVIA,INST CLIN NEUROL,I-27100 PAVIA,ITALY
[7] OSPED MAGGIORE,POLICLIN MILAN,DEPT CARDIOL,MILAN,ITALY
关键词
MITOCHONDRIAL MYOPATHY; UBIQUINONE; MTDNA DELETION;
D O I
10.1016/0022-510X(90)90015-F
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Forty-four patients with mitochondrial myopathies were treated with Ubidecarenone (CoQ10) for 6 months in an open multi-center trial. No side effects of the drug were observed. Sixteen patients showing at least 25% decrease of post-exercise lactate levels were selected as responders. Responsiveness was apparently not related to CoQ10 level in serum and platelets or to the presence or absence of mtDNA deletions. The responders were treated for a further 3 months with CoQ10 or placebo in the second blind part of the trial; no significant differences were observed between the 2 groups. It is not clear why CoQ10 had therapeutic effects in some patients and not in others with the same clinical presentation and biochemical defect, and we failed to identify candidate responders before treatment. At the dose of CoQ10 used in this study (2 mg/kg/day) the therapy requires a long administration time before a response is seen.
引用
收藏
页码:70 / 78
页数:9
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