Center for Movement Disorders, Department of Neurology, Beijing Tiantan Hospital, Capital Medical University, Beijing, 100070, China.
China National Clinical Research Center for Neurological Diseases, Beijing, China.
Neurol Sci. 2022 May;43(5):3165-3174. doi: 10.1007/s10072-021-05694-1. Epub 2021 Dec 1.
With the levodopa threshold effect for dyskinesia observed, threshold dosage of levodopa was identified in the general Parkinson's disease (PD) population. While early-onset PD (EOPD) and late-onset PD (LOPD) differ in the pathogenesis and clinical manifestations, threshold dosage of levodopa for individualized treatment remains unestablished. The objective of this study was to propose threshold dosage of levodopa in EOPD and LOPD patients, respectively.
Data on demographic and clinical and treatment measures were collected in 539 PD patients. Patients were divided into different onset groups using 50 as the cut-off age. We used univariable and multivariable analysis to screen for risk factors for dyskinesia. Receiver operating characteristic curve was used to determine the levodopa threshold dosages for dyskinesia.
The prevalence of dyskinesia was 47.7% (53/111) in the EOPD group and 24.1% (103/428) in the LOPD group. Risk factors identified for dyskinesia include high levodopa daily dose and levodopa responsiveness for EOPD patients and high levodopa daily dose, long levodopa treatment duration, low body weight, use of entacapone, and high Hoehn-Yahr stage in off state for LOPD patients. The daily levodopa threshold dosages were 400 mg or 5.9 mg/kg for EOPD and 450 mg or 7.2 mg/kg for LOPD.
EOPD patients had lower levodopa threshold dosage comparing with LOPD patients. Treatment of EOPD requires stricter levodopa dose control to delay the onset of dyskinesia.
随着发现左旋多巴引发运动障碍的阈值效应,一般帕金森病(PD)患者的左旋多巴阈值剂量得以确定。虽然早发性 PD(EOPD)和晚发性 PD(LOPD)在发病机制和临床表现上有所不同,但个体化治疗的左旋多巴阈值剂量尚未确定。本研究旨在分别为 EOPD 和 LOPD 患者提出左旋多巴的阈值剂量。
收集了 539 名 PD 患者的人口统计学、临床和治疗措施数据。使用 50 岁作为截止年龄将患者分为不同的发病组。我们使用单变量和多变量分析筛选运动障碍的危险因素。使用受试者工作特征曲线确定左旋多巴引发运动障碍的阈值剂量。
EOPD 组运动障碍的患病率为 47.7%(53/111),LOPD 组为 24.1%(103/428)。EOPD 患者运动障碍的危险因素包括左旋多巴的高日剂量和对左旋多巴的高反应性,而 LOPD 患者的危险因素包括左旋多巴的高日剂量、长的左旋多巴治疗持续时间、低体重、使用恩他卡朋和停用时的 Hoehn-Yahr 分期高。EOPD 和 LOPD 的每日左旋多巴阈值剂量分别为 400mg 或 5.9mg/kg 和 450mg 或 7.2mg/kg。
与 LOPD 患者相比,EOPD 患者的左旋多巴阈值剂量较低。EOPD 的治疗需要更严格的左旋多巴剂量控制,以延迟运动障碍的发生。