Lees Andrew
Reta Lila Weston Institute of Neurological Sciences, University College London, London, UK.
Drugs Aging. 2005;22(9):731-40. doi: 10.2165/00002512-200522090-00002.
Parkinson's disease (PD) is primarily a disease of elderly patients. This article reviews current knowledge and recent developments relating to drugs that can be used as alternatives to levodopa as initial treatment of PD. Synthetic orally acting dopamine agonists have found increasing favour as an option for early PD in relatively young patients. This strategy is based on evidence that this approach may delay the onset of motor fluctuations, at least during the first 5 years of treatment. Subcutaneous apomorphine infusions may attenuate motor fluctuations in late-stage disease, and transdermal rotigotine, a dopamine agonist in development, has also been shown to be efficacious. The greater proclivity for dopamine agonists to cause psychotoxicity has, however, limited their routine use in the elderly. Selective monoamine oxidase type B (MAO-B) inhibitors, used as monotherapy, delay the need for the introduction of levodopa by about 9 months. These agents appear to be less efficacious than dopamine agonists but are better tolerated. Concern has been expressed about the potential of the MAO-B inhibitor selegiline (deprenyl) to induce cardiovascular adverse effects (orthostatic hypotension), either directly or through its amphetamine catabolites. Rasagiline is a new MAO-B inhibitor that is not broken down to amphetamine derivatives and is indicated as both monotherapy in early PD and as adjunctive therapy in PD patients with motor fluctuations. Two older classes of agents have undergone a resurgence of interest in recent years. Amantadine, which enhances dopaminergic transmission and has antiglutamate activity, is occasionally used as monotherapy but has recently been widely used as an antidyskinetic agent in late-stage PD. Anticholinergic drugs, such as benztropine (benzatropine) and orphenadrine also provide control of symptoms when used as monotherapy, but their psychotoxic, cognitive and autonomic adverse events make them inappropriate for the treatment of the elderly. Effective therapy in PD should prevent disease progression and abolish motor and cognitive handicap. Currently, none of the existing drugs meets all these needs.
帕金森病(PD)主要是一种老年患者的疾病。本文综述了有关可作为左旋多巴替代药物用于PD初始治疗的药物的现有知识和最新进展。合成口服多巴胺激动剂在相对年轻的PD患者早期治疗中越来越受到青睐。这一策略基于这样的证据,即这种方法可能会延迟运动波动的出现,至少在治疗的前5年是如此。皮下注射阿扑吗啡可减轻晚期疾病的运动波动,正在研发的多巴胺激动剂透皮罗替戈汀也已显示出疗效。然而,多巴胺激动剂更容易引起精神毒性,这限制了它们在老年人中的常规使用。选择性单胺氧化酶B型(MAO-B)抑制剂作为单一疗法使用时,可将引入左旋多巴的时间推迟约9个月。这些药物似乎不如多巴胺激动剂有效,但耐受性更好。有人担心MAO-B抑制剂司来吉兰(丙炔苯丙胺)可能直接或通过其安非他明代谢产物诱发心血管不良反应(体位性低血压)。雷沙吉兰是一种新的MAO-B抑制剂,不会分解为安非他明衍生物,适用于PD早期的单一疗法以及有运动波动的PD患者的辅助治疗。近年来,两类较老的药物重新引起了人们的关注。金刚烷胺可增强多巴胺能传递并具有抗谷氨酸活性,偶尔用作单一疗法,但最近已广泛用作晚期PD的抗运动障碍药物。抗胆碱能药物,如苯海索(苄托品)和奥芬那君,作为单一疗法使用时也可控制症状,但其精神毒性、认知和自主神经不良反应使其不适用于老年患者的治疗。PD的有效治疗应防止疾病进展并消除运动和认知障碍。目前,现有的药物都无法满足所有这些需求。