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

机译:中国帕金森氏病患者出现左旋多巴磨损现象的危险因素和安全剂量

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摘要

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.
机译:这项研究的目的是调查帕金森氏病(PD)的磨损现象的危险因素,并根据中国人群的建议,提出左旋多巴的安全剂量以减少磨损现象。招募了服用左旋多巴(l-dopa)至少1个月的PD患者。根据经验证的中文自我评估的9项穿用量表(WOQ-9)和临床定义,对穿用量进行诊断。 11个变量(性别,左旋多巴开始时的疾病持续时间,评估时的疾病持续时间,发病年龄,评估时的年龄,HY阶段,UPDRS III,左旋多巴的每日总剂量和根据体重调整的剂量,左旋多巴的治疗持续时间(初始药物配方)包括在我们的分析中。采用单因素分析,多元逻辑回归分析和决策树分类模型(DTC)来检测磨损的风险因素。接受者工作特征(ROC)曲线和DTC用于研究左旋多巴的临界值,以最佳地预测磨损。在我们的研究中对234例患者进行了调查,其中111例出现了磨损。疲倦的患者倾向于接受更高的左旋多巴剂量,并承受更长的左旋多巴治疗时间。 ROC的l-Dopa剂量为281 mg / day和4.2 mg / kg / day,DTC的269 mg / day和3.2 mg / kg / day是消减的临界值。左旋多巴的剂量和左旋多巴治疗的持续时间与衰老的发展有关。左旋多巴的累积剂量和左旋多巴的每日剂量可以更好地预测磨损。没有足够的证据表明延迟的l-多巴启动。左旋多巴每日剂量不超过275 mg或4.2 mg / kg被认为是安全的。

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