Department of Neurology, National Center Hospital, National Center of Neurology and Psychiatry, Tokyo, Japan; Department of Neurology, Juntendo University School of Medicine, Tokyo, Japan.
Data Tecnica International, Glen Echo, MD, USA.
Parkinsonism Relat Disord. 2023 Sep;114:105798. doi: 10.1016/j.parkreldis.2023.105798. Epub 2023 Aug 6.
It is known that the pharmacokinetics (PK) of levodopa (LD) varies considerably. Difference in PK shapes is expected to affect drug efficacy and development of dyskinesia. In this study, the authors aimed to explore correlations between PK series data of LD and clinical characteristics and dyskinesia in patients with Parkinson's disease (PD).
We studied 270 PD patients who underwent PK assessment after administration of LD/carbidopa (100/10 mg) in non-compartmental analysis. The patients were grouped according to similarities in time series data of blood LD concentration. Each group was analyzed with respect to clinical characteristics and PK parameters. We created a model to predict PK patterns based on these findings.
PD patients were divided into three groups by clustering analysis: blood LD concentration of the patients in Groups 1 (n = 129), 3 (n = 44) and 2 (n = 97) rose rapidly, relatively slowly and at an intermediate rate, respectively. There were no statistically significant differences in patient characteristics except age among the three groups (one-way ANOVA). Multivariate analysis showed that frequency of dyskinesias in Group 1 was significantly higher than that in Group 2. We successfully created a PK pattern prediction model based on body weight and blood LD concentration at 15 and 30 min after administration.
The PK series data of LD was classified into three patterns. The rapid absorption was associated with dyskinesias. Patients' PK patterns were successfully predicted based on their body weight and two-point LD concentration.
左旋多巴(LD)的药代动力学(PK)变化很大。PK 形状的差异预计会影响药物疗效和运动障碍的发展。在这项研究中,作者旨在探索 PD 患者 LD 的 PK 系列数据与临床特征和运动障碍之间的相关性。
我们研究了 270 名 PD 患者,他们在非房室分析中接受了 LD/卡比多巴(100/10mg)给药后的 PK 评估。根据血 LD 浓度时间序列数据的相似性,将患者分组。对每组进行临床特征和 PK 参数分析。我们根据这些发现创建了一个预测 PK 模式的模型。
通过聚类分析,PD 患者分为三组:第 1 组(n=129)、第 3 组(n=44)和第 2 组(n=97)患者的血 LD 浓度升高迅速、相对缓慢和中等速度。三组患者的特征除年龄外无统计学差异(单因素方差分析)。多变量分析显示,第 1 组的运动障碍频率明显高于第 2 组。我们成功地基于给药后 15 分钟和 30 分钟的体重和血 LD 浓度创建了 PK 模式预测模型。
LD 的 PK 系列数据分为三种模式。快速吸收与运动障碍有关。患者的 PK 模式可以根据体重和两点 LD 浓度成功预测。