Shoulson I
Department of Neurology, University of Rochester, NY 14620, USA.
Ann Neurol. 1998 Sep;44(3 Suppl 1):S160-6.
In 1987, the DATATOP clinical trial was initiated to examine the benefits of deprenyl (selegiline) and alpha-tocopherol in slowing the progression of Parkinson's disease (PD). After 14 +/- 6 (mean +/- SD) months of controlled observation, deprenyl 10 mg/day was found to significantly delay the time until enough disability developed to warrant the initiation of levodopa therapy. This effect was largely sustained during the overall 8.2 years of observation, including open-label deprenyl treatment and a second treatment randomization to continue deprenyl or switch to placebo. There were no accompanying benefits of deprenyl in postponing levodopa-related adverse effects or extending life. Alpha-tocopherol produced no benefits. The 2.1% per year mortality rate of the DATATOP cohort was remarkably low, about the same as an age-matched population without PD. Neuroprotective therapy remains an elusive goal for the experimental therapeutics of PD. Advances in understanding pathogenesis, a robust pipeline of rational treatments, and the advent of valid and reliable biologic markers hold promise in the coming decade for developing and achieving neuroprotective therapies for PD.
1987年,启动了DATATOP临床试验,以研究丙炔苯丙胺(司来吉兰)和α-生育酚在减缓帕金森病(PD)进展方面的益处。经过14±6(均值±标准差)个月的对照观察,发现每天服用10毫克丙炔苯丙胺可显著延迟出现足以启动左旋多巴治疗的残疾症状的时间。在整个8.2年的观察期内,包括开放标签的丙炔苯丙胺治疗以及第二次治疗随机分组以继续使用丙炔苯丙胺或改用安慰剂,这一效果基本得以维持。丙炔苯丙胺在推迟左旋多巴相关不良反应或延长寿命方面并无附带益处。α-生育酚也未产生任何益处。DATATOP队列每年2.1%的死亡率极低,与无PD的年龄匹配人群大致相同。神经保护疗法仍是PD实验性治疗难以实现的目标。在理解发病机制方面的进展、合理治疗的强大研发流程以及有效可靠生物标志物的出现,有望在未来十年为开发和实现PD的神经保护疗法带来希望。