Department of Neuroscience, Uppsala Department of Pharmacy, Uppsala University, Uppsala, Sweden.
Eur J Neurol. 2012 Jun;19(6):820-6. doi: 10.1111/j.1468-1331.2011.03614.x. Epub 2011 Dec 5.
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.
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.
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.
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.
儿茶酚-O-甲基转移酶抑制剂可用于减少左旋多巴的需求。目的是研究当添加口服儿茶酚-O-甲基转移酶抑制剂时,左旋多巴/卡比多巴肠凝胶输注剂量是否可以减少 20%,而不会恶化运动波动和左旋多巴浓度稳定性。
进行了一项短期、随机、部分盲、交叉、研究者发起的临床试验,10 名患者在两天内接受左旋多巴/卡比多巴肠凝胶联合口服恩他卡朋和托卡朋治疗。主要观察指标是血浆左旋多巴变异系数的差异,左旋多巴/卡比多巴、左旋多巴/卡比多巴/恩他卡朋和左旋多巴/卡比多巴/托卡朋之间的差异。次要观察指标包括其他药代动力学变量、患者报告的结果和运动表现的盲法分析。
治疗组之间血浆左旋多巴浓度的变异无显著差异。治疗组之间的运动表现无差异。托卡朋的左旋多巴浓度明显更高。儿茶酚-O-甲基转移酶抑制期间,代谢产物 3-O-甲基多巴的浓度逐渐下降。
根据这项小规模、短期的初步研究,在 5 小时间隔给予口服儿茶酚-O-甲基转移酶抑制剂可能适用于希望减少左旋多巴/卡比多巴肠凝胶剂量的情况。当减少左旋多巴/卡比多巴肠凝胶剂量 20%时,血浆左旋多巴水平的稳定性不会显著改变,并且不会增加无活动期。相反,剂量可能应该减少超过 20%,特别是在托卡朋联合治疗下,以避免随着时间的推移增加运动障碍。