Department of Neurology, Parkinson's Disease Center and Movement Disorder Clinic, Baylor College of Medicine, 7200 Cambridge, Suite 9A, Houston, TX, 77030-4202, USA.
Drugs. 2016 May;76(7):759-77. doi: 10.1007/s40265-016-0566-3.
Dyskinesias encompass a variety of different hyperkinetic phenomenologies, particularly chorea, dystonia, stereotypies, and akathisia. Levodopa-induced dyskinesia (LID) is one of the main types of drug-induced dyskinesia, occurring in patients with Parkinson's disease (PD) who have been treated with levodopa for long time, but this side effect may be encountered even within a few weeks or months after initiation of levodopa therapy. Based on the temporal pattern in relationship to levodopa dosing, LIDs are divided into "peak-dose dyskinesia," "diphasic dyskinesia," and "wearing off" or "off-period" dyskinesia, of which peak-dose dyskinesia is the most common, followed by off-period, and then diphasic dyskinesia. Treatment strategy includes identifying the kind of dyskinesia and tailoring treatment accordingly. Peak-dose dyskinesia is treated mainly by reducing individual doses of levodopa and adding amantadine and dopamine agonists, whereas off-period dystonia often responds to baclofen and botulinum toxin injections. Diphasic dyskinesias, occurring particularly in patients with young-onset PD, are the most difficult to treat. While fractionation of levodopa dosage is the most frequently utilized strategy, many patients require deep brain stimulation to control their troublesome motor fluctuations and LIDs. A variety of emerging (experimental) drugs currently in development promise to provide better control of LIDs and other levodopa-related complications in the near future.
不自主运动包括多种不同的运动障碍现象,特别是舞蹈症、肌张力障碍、刻板动作和静坐不能。左旋多巴诱导的不自主运动(LID)是药物诱导的不自主运动的主要类型之一,发生在长期接受左旋多巴治疗的帕金森病(PD)患者中,但即使在开始左旋多巴治疗后的数周或数月内也可能出现这种副作用。根据与左旋多巴剂量的时间模式,LIDs 分为“峰剂量不自主运动”、“双相不自主运动”和“开期或结束期”不自主运动,其中峰剂量不自主运动最常见,其次是结束期,然后是双相不自主运动。治疗策略包括确定不自主运动的类型并相应地进行治疗。峰剂量不自主运动主要通过减少左旋多巴的个体剂量和添加金刚烷胺和多巴胺激动剂来治疗,而结束期肌张力障碍通常对巴氯芬和肉毒毒素注射有反应。双相不自主运动,特别是在年轻发病的 PD 患者中,最难治疗。虽然左旋多巴剂量的分割是最常用的策略,但许多患者需要深部脑刺激来控制他们的运动波动和 LIDs。目前正在开发的各种新兴(实验)药物有望在不久的将来提供更好的 LID 和其他与左旋多巴相关的并发症控制。