Department of Neurology, Centro Hospitalar Universitário de S. João, Alameda Prof. Hernâni Monteiro, 4200-319, Porto, Portugal.
Department of Clinical Neurosciences and Mental Health, Faculty of Medicine, University of Porto, Porto, Portugal.
Drugs. 2019 Apr;79(6):593-608. doi: 10.1007/s40265-019-01098-w.
Parkinson's disease (PD) is a chronic, progressive condition affecting around 1% of the population older than 60 years. Upon long-term treatment with levodopa, the mainstay of treatment in PD, most patients, especially younger ones exposed to higher doses, will experience symptoms related to end-of-dose deterioration, peak-dose dyskinesias, and other motor fluctuations. Therapeutic strategies are grounded on modification of oral levodopa pharmacokinetics to extend levodopa benefit and development of new routes of drug delivery (e.g., levodopa/carbidopa intestinal gel infusion) or long-acting formulations of existing dopaminergic drugs to prolong the duration of striatal dopamine receptors stimulation. As our understanding of the pathophysiology of motor complications evolves, our therapeutic armamentarium is actively expanding and the focus of research is now actively pointing to the new non-dopaminergic agents acting both within the basal ganglia and in other brain regions (e.g., drugs acting on glutamate, GABA, serotonin, and calcium channels). Despite the fact that trials comparing the different therapeutic strategies are lacking, we aimed at devising practical evidence- and experience-guided suggestions for the clinical management of motor complications, emphasizing that this should always be an individualized endeavor. This review summarizes the pharmacological management of motor complications in PD, including new formulations and routes of delivery, and the newer released drugs such as istradefylline, opicapone, safinamide, and zonisamide. Advanced therapeutic strategies for selected cases such as treatment with apomorphine and surgical techniques (deep brain stimulation) are also discussed. A comprehensive knowledge of the available options and evidence is fundamental for the successful management of these challenging complications.
帕金森病(PD)是一种慢性、进行性疾病,影响着 60 岁以上人群的 1%左右。在长期接受左旋多巴治疗(PD 的主要治疗方法)后,大多数患者,尤其是接触较高剂量的年轻患者,会出现与剂量末恶化、峰剂量运动障碍和其他运动波动相关的症状。治疗策略基于改变口服左旋多巴的药代动力学,以延长左旋多巴的益处,并开发新的药物输送途径(例如,左旋多巴/卡比多巴肠凝胶输注)或现有的多巴胺能药物的长效制剂,以延长纹状体多巴胺受体刺激的持续时间。随着我们对运动并发症病理生理学的理解不断发展,我们的治疗手段正在积极扩展,研究的重点现在积极指向新的非多巴胺能药物,这些药物既作用于基底神经节,也作用于其他脑区(例如,作用于谷氨酸、GABA、血清素和钙通道的药物)。尽管缺乏比较不同治疗策略的试验,但我们旨在为运动并发症的临床管理制定实用的基于证据和经验的建议,强调这始终应该是一项个体化的努力。这篇综述总结了 PD 中运动并发症的药物治疗,包括新的制剂和输送途径,以及新发布的药物,如依他司琼、opiCapone、沙芬酰胺和唑尼沙胺。还讨论了针对选定病例的高级治疗策略,如阿扑吗啡治疗和手术技术(深部脑刺激)。全面了解现有选择和证据对于成功管理这些具有挑战性的并发症至关重要。