Ghika J, Tennis M, Hoffman E, Schoenfeld D, Growdon J
Department of Neurology, Massachusetts General Hospital, Boston 02114.
Neurology. 1991 Jul;41(7):986-91. doi: 10.1212/wnl.41.7.986.
To confirm the preliminary report that increases in norepinephrine neurotransmission improve motor performance, we administered the investigational drug idazoxan (IDA) to nine patients with progressive supranuclear palsy (PSP) according to a double-blind crossover protocol. There were seven women and two men, whose mean age was 70 years and mean duration of illness 4 years. All had an advanced parkinsonian syndrome, supranuclear ocular motor palsies, and poor responses to dopaminergic drugs. During administration of 40 mg tid of IDA, the total score and the motor subscale score of the United Parkinson's Disease Rating Scale significantly decreased. Features that improved most included mobility, balance, gait, and measures of digital dexterity. There were no significant changes in any measure during placebo administration. Corticobulbar manifestations and eye movements were not significantly improved during treatment. Side effects of IDA included transient hypertension, tachycardia, action tremor, flushing, and sweating, but none was so severe that any patient withdrew from the study. Among the few attempted treatments of PSP, IDA is the first medication shown in a double-blind study to improve aspects of motor function.
为证实去甲肾上腺素神经传递增加可改善运动表现的初步报告,我们按照双盲交叉方案,对9例进行性核上性麻痹(PSP)患者给予了研究药物咪唑克生(IDA)。患者中有7名女性和2名男性,平均年龄70岁,平均病程4年。所有患者均患有晚期帕金森综合征、核上性眼球运动麻痹,且对多巴胺能药物反应不佳。在给予IDA每日3次、每次40mg的过程中,统一帕金森病评定量表的总分及运动分量表得分显著降低。改善最明显的特征包括活动能力、平衡能力、步态以及手指灵活性指标。在给予安慰剂期间,各项指标均无显著变化。治疗期间,皮质延髓表现和眼球运动未得到显著改善。IDA的副作用包括短暂性高血压、心动过速、动作性震颤、面部潮红和出汗,但均未严重到使任何患者退出研究。在为数不多的针对PSP的尝试性治疗中,IDA是首个在双盲研究中显示可改善运动功能的药物。