Schapira Anthony H V
University Department of Clinical Neurosciences, University College London, London NW3 2PF, UK.
Trends Pharmacol Sci. 2009 Jan;30(1):41-7. doi: 10.1016/j.tips.2008.10.005. Epub 2008 Nov 29.
Parkinson's disease (PD) is the second most common neurodegenerative disorder after Alzheimer's disease and is an important cause of chronic disability. Numerous important advances have been made in our understanding of the aetiopathogenesis, pathology and clinical phenomenology of this disease, and these have underpinned advances in symptomatic treatment and the prospect that these might be extended into interventions that will slow progression. It is notable that the continuing characterisation of the downstream biochemical consequences of the genetic causes of PD serves only to reinforce this notion. Progress in the management of PD has continued, particularly in timing of drug initiation and the sequence and combinations in which drugs are used to improve long-term outcome and reduce drug-induced complications. Particular progress has been made in the field of neuroprotection, where novel therapies and clinical trial designs are being tested. This review will focus particularly upon this area.
帕金森病(PD)是仅次于阿尔茨海默病的第二常见神经退行性疾病,是导致慢性残疾的重要原因。我们对该疾病的病因发病机制、病理学和临床现象学的认识取得了许多重要进展,这些进展为对症治疗的进步以及将这些治疗扩展为可能减缓疾病进展的干预措施奠定了基础。值得注意的是,对帕金森病遗传病因的下游生化后果的持续表征只会强化这一观念。帕金森病管理方面持续取得进展,特别是在药物起始时机以及药物使用顺序和组合方面,以改善长期疗效并减少药物引起的并发症。在神经保护领域取得了特别进展,正在测试新的疗法和临床试验设计。本综述将特别关注这一领域。