Thomas A, Iacono D, Luciano A L, Armellino K, Di Iorio A, Onofrj M
Neurophysiopathology, Movement Disorders Centre, Department of Oncology and Neuroscience, Università G. D'Annunzio, Chieti-Pescara, Pescara, Italy.
J Neurol Neurosurg Psychiatry. 2004 Jan;75(1):141-3.
Recent short-term studies suggested that amantadine (Ama) might ameliorate dyskinesia in patients with Parkinson's disease. A double-blind study programmed over 12 months was designed to assess the duration of the antidyskinetic effect of amantadine on levodopa induced dyskinesia.
40 patients treated for 7.5 (2.2) years with levodopa (729.3 (199.4) mg/day) and dopaminoagonists, having peak dose or dyphasic dyskinesia with or without pain, were assessed with the Unified Parkinson's Disease Rating Scale subscale IV, Items 32-34, the Dyskinesia Rating Scale and Investigator Global Assessment. Twenty patients received amantadine chloridrate (100 mg) and 20 received a placebo. The Ama or placebo could be withdrawn when scores indicated worsening of dyskinesia, after agreement with the patient.
After 15 days of amantadine treatment there was a reduction by 45% in the total dyskinesia scores. All patients in the placebo group were withdrawn in 1-3 months and all patients in the Ama group were withdrawn in 3-8 months (p = 0.01, p<0.001). Ama withdrawal induced a rebound with increase of dyskinesia by 10-20% in 11 patients.
300 mg amantadine reduces dyskinesia in Parkinson's disease by approximately 45% but the benefit lasted less than eight months.
近期的短期研究表明,金刚烷胺(Ama)可能改善帕金森病患者的异动症。一项为期12个月的双盲研究旨在评估金刚烷胺对左旋多巴诱发异动症的抗异动症作用持续时间。
40例接受左旋多巴(729.3(199.4)mg/天)和多巴胺激动剂治疗7.5(2.2)年、出现峰值剂量或双相异动症且伴有或不伴有疼痛的患者,采用统一帕金森病评定量表第四部分32 - 34项、异动症评定量表和研究者整体评估进行评估。20例患者接受盐酸金刚烷胺(100 mg),20例接受安慰剂。经与患者协商,当评分显示异动症恶化时,可停用Ama或安慰剂。
金刚烷胺治疗15天后,异动症总评分降低了45%。安慰剂组所有患者在1 - 3个月内停药,Ama组所有患者在3 - 8个月内停药(p = 0.01,p<0.001)。停用Ama导致11例患者异动症反弹,增加了10 - 20%。
300 mg金刚烷胺可使帕金森病异动症减少约45%,但益处持续不到8个月。