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中国帕金森病患者左旋多巴治疗剂末现象的危险因素及安全剂量

Risk factors and safe dosage of levodopa for wearing-off phenomenon in Chinese patients with Parkinson's disease.

作者信息

Chen Huimin, Fang Jinping, Li Fangfei, Gao Liyan, Feng Tao

机构信息

Department of Neurology, Center for Neurodegenerative Disease, Beijing Tiantan Hospital, Capital Medical University, #6 Tian Tan Xi Li Street, 100050, Beijing, China.

出版信息

Neurol Sci. 2015 Jul;36(7):1217-23. doi: 10.1007/s10072-015-2078-4. Epub 2015 Jan 24.

Abstract

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.

摘要

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。

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