Nyholm Dag, Johansson Anders, Aquilonius Sten-Magnus, Hellquist Elisabeth, Lennernäs Hans, Askmark Håkan
Department of Neuroscience, Neurology, Uppsala University, E-75185 Uppsala, Sweden.
Clin Neuropharmacol. 2012 Jan-Feb;35(1):6-14. doi: 10.1097/WNF.0b013e31823b1ffd.
The aim was to elaborately describe individual pharmacokinetic-pharmacodynamic profiles in patients with difficult-to-treat dyskinesias treated with levodopa/carbidopa intestinal gel infusion.
A nonrandomized, partly blinded, investigator-initiated trial was conducted in 5 patients with idiopathic Parkinson disease who were difficult to keep in "on" state without dyskinesia. Levodopa/carbidopa intestinal gel (Duodopa) doses of 80% to 120% of individually and clinically optimized dosage were infused during five 4-hour periods. Pharmacokinetic profiling, blinded assessment of video recordings, and objective movement analysis were applied every 20 to 30 minutes.
Individual correlations between plasma levodopa concentrations and corresponding motor scores 20 to 30 minutes after the sampling time were significant in all patients (P < 0.05 and P < 0.001). Motor scores were generally stable during the 4-hour periods. The objective test revealed that motor performance was faster the more dyskinetic the patients were. Mean individual Treatment Response Scale scores were positive in 24 of the 25 steady-state periods. Dystonia was always combined with choreic dyskinesias.
Motor response from different doses of levodopa/carbidopa intestinal gel is in a broad sense predictable even in dyskinetic patients although major interindividual differences in dose requirement, plasma levels, and motor response are found. That motor performance was faster the more dyskinetic the patients were implies that motor performance may be better with moderate dyskinesia than with mild dyskinesia. This may explain why patients with persistent dyskinesias choose to keep their doses above the dyskinesia threshold. There is no ideal therapeutic window in such patients, but levodopa infusion offers stable motor response.
本研究旨在详细描述左旋多巴/卡比多巴肠凝胶输注治疗难治性运动障碍患者的个体药代动力学-药效学特征。
对5例特发性帕金森病患者进行了一项非随机、部分盲法、研究者发起的试验,这些患者在无运动障碍的情况下难以维持“开”状态。在五个4小时时间段内,输注左旋多巴/卡比多巴肠凝胶(Duodopa),剂量为个体临床优化剂量的80%至120%。每20至30分钟进行一次药代动力学分析、对视频记录进行盲法评估以及客观运动分析。
所有患者在采样时间后20至30分钟时,血浆左旋多巴浓度与相应运动评分之间的个体相关性均显著(P < 0.05和P < 0.001)。在4小时时间段内,运动评分总体稳定。客观测试显示,患者运动障碍越严重,运动表现越快。在25个稳态期的24个中,个体治疗反应量表平均评分呈阳性。肌张力障碍总是与舞蹈样运动障碍同时出现。
即使在存在运动障碍的患者中,不同剂量的左旋多巴/卡比多巴肠凝胶产生的运动反应在广义上也是可预测的,尽管在剂量需求、血浆水平和运动反应方面存在较大的个体差异。患者运动障碍越严重,运动表现越快,这意味着中度运动障碍患者的运动表现可能优于轻度运动障碍患者。这或许可以解释为什么持续性运动障碍患者会选择将剂量维持在运动障碍阈值以上。此类患者不存在理想的治疗窗,但左旋多巴输注可提供稳定的运动反应。