首页> 外文期刊>European journal of neurology: the official journal of the European Federation of Neurological Societies >Levodopa infusion combined with entacapone or tolcapone in Parkinson disease: A pilot trial
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Levodopa infusion combined with entacapone or tolcapone in Parkinson disease: A pilot trial

机译:左旋多巴输注联合恩他卡朋或托卡朋治疗帕金森病:一项先导试验

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Background and purpose: Catechol-O-methyltransferase inhibitors may be used to decrease levodopa requirement. The objective was to investigate whether the levodopa/carbidopa intestinal gel infusion dose can be reduced by 20% without worsening of motor fluctuations and levodopa concentration stability when oral catechol-O-methyltransferase inhibitors are added. Methods: A short-term, randomized, partly blinded, crossover, investigator-initiated clinical trial was performed, with levodopa/carbidopa intestinal gel combined with oral entacapone and tolcapone on two different days in 10 patients. The primary outcome measure was difference in coefficient of variation of levodopa in plasma between levodopa/carbidopa, levodopa/carbidopa/entacapone, and levodopa/carbidopa/tolcapone. The secondary outcome measures other pharmacokinetic variables, patient-reported outcome, and blinded analysis of motor performance. Results: Variation of plasma levodopa concentrations did not differ significantly between the treatments. The treatments did not differ regarding motor performance. Levodopa concentrations were significantly higher using tolcapone. Concentrations of the metabolite 3-O-methyldopa decreased gradually during catechol-O-methyltransferase inhibition. Conclusions: According to this small, short-term pilot study, oral catechol-O-methyltransferase inhibitors administered in 5-h intervals may be useful in cases where levodopa/carbidopa intestinal gel dose reduction is wanted. Stability of plasma levodopa levels is not significantly altered, and off-time is not increased when decreasing the levodopa/carbidopa intestinal gel dose by 20%. Rather, the dose should probably be decreased more than 20%, especially under tolcapone co-treatment, to avoid increased dyskinesias with time.
机译:背景和目的:儿茶酚-O-甲基转移酶抑制剂可用于降低左旋多巴的需求量。目的是研究添加口服儿茶酚-O-甲基转移酶抑制剂后,左旋多巴/卡比多巴肠道凝胶输注剂量是否可降低20%,而不会增加运动波动和左旋多巴浓度稳定性。方法:一项短期,随机,部分盲法,交叉,研究者发起的临床试验进行了研究,其中左旋多巴/卡比多巴肠凝胶联合口服恩他卡朋和托卡朋分别在10天中进行。主要结局指标为左旋多巴/卡比多巴,左旋多巴/卡比多巴/他卡朋和左旋多巴/卡比多巴/托卡朋之间血浆左旋多巴变异系数的差异。次要结局可衡量其他药代动力学变量,患者报告的结局以及运动表现的盲目分析。结果:各治疗之间血浆左旋多巴浓度的变化无明显差异。治疗方法在运动表现方面没有差异。使用托卡朋时左旋多巴的浓度明显更高。在儿茶酚-O-甲基转移酶抑制过程中,代谢物3-O-甲基多巴的浓度逐渐降低。结论:根据这项小型的短期试验研究,在希望降低左旋多巴/卡比多巴肠凝胶剂量的情况下,每隔5小时服用一次口服儿茶酚-O-甲基转移酶抑制剂可能是有用的。将左旋多巴/卡比多巴肠凝胶剂量降低20%时,血浆左旋多巴水平的稳定性没有明显改变,关闭时间也没有增加。相反,剂量应减少超过20%,尤其是在托卡朋共同治疗下,以避免随时间增加运动障碍。

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