Mov Disord. 1999 Jan;14(1):38-44.
The catechol-O-methyltransferase inhibitor tolcapone was compared with the dopamine agonist bromocriptine in an open-label, randomized trial involving 146 levodopa-treated parkinsonian patients with end-of-dose deterioration of efficacy. Tolcapone was given at a dosage of 200 mg three times daily; bromocriptine was titrated from 1.25 mg once daily at baseline to, at most, 10 mg three times daily by day 24 (mean final dose 22.4 mg/day). After 8 weeks, the tolcapone group had a significant reduction in daily levodopa dose compared with the bromocriptine group (p<0.05). No significant differences in the "on/off" time and motor disability were seen between the tolcapone and bromocriptine treatment groups. Bromocriptine induced more hallucinations, orthostatic hypotension, and nausea, whereas tolcapone therapy was associated with more muscle cramps and dystonia. These results suggest that when added to levodopa therapy, the two drugs have a different side effect profile, with the advantages for tolcapone being absence of titration and quicker efficacy.
在一项开放性随机试验中,将儿茶酚-O-甲基转移酶抑制剂托卡朋与多巴胺激动剂溴隐亭进行了比较,该试验涉及146名接受左旋多巴治疗且出现疗效剂末恶化的帕金森病患者。托卡朋的给药剂量为每日3次,每次200毫克;溴隐亭从基线时每日1次,每次1.25毫克开始滴定,到第24天时最多每日3次,每次10毫克(平均最终剂量为22.4毫克/天)。8周后,与溴隐亭组相比,托卡朋组的每日左旋多巴剂量显著降低(p<0.05)。托卡朋治疗组和溴隐亭治疗组之间在“开/关”时间和运动功能障碍方面未见显著差异。溴隐亭引起更多幻觉、体位性低血压和恶心,而托卡朋治疗则与更多肌肉痉挛和肌张力障碍有关。这些结果表明,在左旋多巴治疗中添加这两种药物时,它们具有不同的副作用特征,托卡朋的优势在于无需滴定且起效更快。