Chen Huimin, Fang Jinping, Li Fangfei, Gao Liyan, Feng Tao
Department of Neurology, Center for Neurodegenerative Disease, Beijing Tiantan Hospital, Capital Medical University, #6 Tian Tan Xi Li Street, 100050, Beijing, China.
Neurol Sci. 2015 Jul;36(7):1217-23. doi: 10.1007/s10072-015-2078-4. Epub 2015 Jan 24.
The objective of this study was to investigate the risk factors of wearing-off phenomenon in Parkinson's disease (PD) and propose safe dosage of levodopa to reduce wearing-off development based on Chinese cohort. Patients with PD who had taken levodopa (L-dopa) for at least 1 month were recruited. Wearing-off was diagnosed based on validated Chinese version of a patient self-rated 9-question Wearing-Off Questionnaire (WOQ-9) and clinical definition. Eleven variables (gender, disease duration at L-dopa initiation, disease duration at assessment, age at onset, age at assessment, H-Y stage, UPDRS III, L-dopa daily total dosage and dosage adjusted to weight, duration of L-dopa treatment, initial drug recipe) were included in our analysis. Univariate analysis, multivariate logistic regression analysis and decision tree classification model(DTC) were used to detect risk factors of wearing-off. Receiver operating characteristic (ROC) curve and DTC were used to investigate cut-off value of L-dopa to best predict wearing-off. Two hundred and thirty-four patients were investigated in our study, among whom 111 developed wearing-off. Patients with wearing-off tended to receive higher L-dopa dosage and endure longer duration of L-dopa treatment. L-Dopa dosage as 281 mg/day and 4.2 mg/kg/day by ROC, as well as 269 mg/day and 3.2 mg/kg/day by DTC were cut-off values for wearing-off. L-Dopa dosage and duration of L-dopa treatment were related to increased wearing-off development. Cumulative L-dopa dosage and L-dopa daily dosage were better predictive of wearing-off. Inadequate evidence was present for delayed L-dopa initiation. L-Dopa daily dosage no more than 275 mg or 4.2 mg/kg was regarded as safe.
本研究的目的是调查帕金森病(PD)中剂末现象的危险因素,并基于中国队列提出左旋多巴的安全剂量以减少剂末现象的发生。招募了服用左旋多巴(L-多巴)至少1个月的PD患者。根据经过验证的中文版患者自评9题剂末现象问卷(WOQ-9)和临床定义诊断剂末现象。我们的分析纳入了11个变量(性别、开始使用L-多巴时的病程、评估时的病程、发病年龄、评估时的年龄、H-Y分期、UPDRS III评分、L-多巴每日总剂量及按体重调整后的剂量、L-多巴治疗时长、初始用药方案)。采用单因素分析、多因素逻辑回归分析和决策树分类模型(DTC)来检测剂末现象的危险因素。采用受试者工作特征(ROC)曲线和DTC来研究L-多巴的最佳预测剂末现象的截断值。本研究共调查了234例患者,其中111例出现了剂末现象。出现剂末现象的患者往往接受更高剂量的L-多巴且L-多巴治疗时长更长。ROC曲线得出的L-多巴剂量截断值为281mg/天和4.2mg/(kg·天),DTC得出的截断值为269mg/天和3.2mg/(kg·天)用于预测剂末现象。L-多巴剂量和L-多巴治疗时长与剂末现象发生增加有关。累积L-多巴剂量和L-多巴每日剂量对剂末现象的预测效果更好。L-多巴起始延迟的证据不足。L-多巴每日剂量不超过275mg或4.2mg/kg被视为安全剂量。