Hely M A, Morris J G
Department of Neurology, Westmead Hospital, Sydney, New South Wales, Australia.
Curr Opin Neurol. 1996 Aug;9(4):308-13. doi: 10.1097/00019052-199608000-00012.
Although theoretical reasons exist for believing that selegiline slows the progression of Parkinson's disease, this has not been shown in clinical trials. Selegiline improves the symptoms of Parkinson's disease, allowing the introduction of levodopa to be delayed in de-novo patients and, later, for levodopa to be used at a lower dose. It does not lessen the long-term problems of dyskinesia and fluctuations associated with levodopa therapy. The report of an increased mortality associated with selegiline therapy awaits further evaluation. Of the dopamine agonists, pergolide appears to be more potent than bromocriptine; cabergoline looks promising. The catechol-O-methyltransferase inhibitors, tolcapone and entacopone, prolong the duration of action of levodopa and also show promise. The main objective in the drug treatment of Parkinson's disease remains the optimization of the dose and frequency of levodopa administration.
虽然有理论依据认为司来吉兰可减缓帕金森病的进展,但临床试验中尚未得到证实。司来吉兰可改善帕金森病症状,使初发患者延迟使用左旋多巴,且之后可降低左旋多巴的使用剂量。它并不能减轻与左旋多巴治疗相关的运动障碍和症状波动等长期问题。关于司来吉兰治疗导致死亡率增加的报告尚待进一步评估。在多巴胺激动剂中,培高利特似乎比溴隐亭更有效;卡麦角林前景看好。儿茶酚-O-甲基转移酶抑制剂托卡朋和恩他卡朋可延长左旋多巴的作用时间,也显示出前景。帕金森病药物治疗的主要目标仍然是优化左旋多巴给药的剂量和频率。