Department of Neurology, Showa University Fujigaoka Hospital, Japan.
Department of Neurology, Showa University Fujigaoka Hospital, Japan.
J Neurol Sci. 2022 Jun 15;437:120263. doi: 10.1016/j.jns.2022.120263. Epub 2022 Apr 18.
In Japan, only two medications of immediate-release levodopa with distinct ratios of decarboxylase inhibitor (DCI), namely levodopa/benserazide 100/25 mg and levodopa/carbidopa 100/10 mg, are available for the treatment of Parkinson's disease (PD). The relationship between the difference in the DCI to levodopa ratio and the development of motor complications in long-term administration of levodopa is unknown.
We assessed the duration from initiation of levodopa/DCI to the emergence of motor fluctuations in patients with PD treated with levodopa/benserazide and levodopa/carbidopa.
We retrospectively assessed the disease course, especially the period from the onset of motor symptoms or initiation of levodopa/DCI to the emergence of motor fluctuations, in patients with PD who were initially treated with either levodopa/benserazide (300/75 mg/day) or levodopa/carbidopa (300/30 mg/day).
Of the 186 candidates, 52 patients were enrolled. The mean duration to the emergence of motor fluctuations in the levodopa/carbidopa group was significantly longer than that in the levodopa/benserazide group (5.0 ± 1.4 vs 3.1 ± 1.2 years, p < 0.01). The mean duration from onset of motor symptoms to the emergence of motor fluctuations in the levodopa/carbidopa group was also significantly longer than that in the levodopa/benserazide group (6.6 ± 1.6 vs 4.7 ± 1.3 years, p < 0.01).
Our study suggests that levodopa/carbidopa therapy with a DCI to levodopa ratio of 1:10 may delay the occurrence of motor fluctuations when compared to levodopa/benserazide therapy with that of 1:4. The difference in the blending ratio of levodopa/DCI may influence the disease progression in PD.
在日本,只有两种即刻释放型左旋多巴药物与不同比例的脱羧酶抑制剂(DCI),即左旋多巴/苄丝肼 100/25mg 和左旋多巴/卡比多巴 100/10mg,可用于治疗帕金森病(PD)。左旋多巴长期给药时,DCI 与左旋多巴比值的差异与运动并发症的发展之间的关系尚不清楚。
我们评估了接受左旋多巴/苄丝肼和左旋多巴/卡比多巴治疗的 PD 患者从开始使用左旋多巴/ DCI 到出现运动波动的时间。
我们回顾性评估了患者的疾病进程,特别是从运动症状发作或开始使用左旋多巴/ DCI 到出现运动波动的时间,这些患者最初接受左旋多巴/苄丝肼(300/75mg/天)或左旋多巴/卡比多巴(300/30mg/天)治疗。
在 186 名候选人中,有 52 名患者入选。左旋多巴/卡比多巴组出现运动波动的平均时间明显长于左旋多巴/苄丝肼组(5.0±1.4 年 vs 3.1±1.2 年,p<0.01)。左旋多巴/卡比多巴组从运动症状发作到出现运动波动的平均时间也明显长于左旋多巴/苄丝肼组(6.6±1.6 年 vs 4.7±1.3 年,p<0.01)。
我们的研究表明,与左旋多巴/苄丝肼 1:4 的配比相比,DCI 与左旋多巴的配比为 1:10 的左旋多巴/卡比多巴治疗可能会延迟运动波动的发生。左旋多巴/ DCI 的混合比例差异可能会影响 PD 的疾病进展。