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GDNF 与帕金森病:未来之路?近期研讨会总结。

GDNF and Parkinson's Disease: Where Next? A Summary from a Recent Workshop.

机构信息

Cambridge Centre for Brain Repair, Department of Clinical Neuroscience and WT-MRC Cambridge Stem Cell Institute, Cambridge, UK.

Wallenberg Neuroscience Center, Lund University, Lund, Sweden.

出版信息

J Parkinsons Dis. 2020;10(3):875-891. doi: 10.3233/JPD-202004.

Abstract

The concept of repairing the brain with growth factors has been pursued for many years in a variety of neurodegenerative diseases including primarily Parkinson's disease (PD) using glial cell line-derived neurotrophic factor (GDNF). This neurotrophic factor was discovered in 1993 and shown to have selective effects on promoting survival and regeneration of certain populations of neurons including the dopaminergic nigrostriatal pathway. These observations led to a series of clinical trials in PD patients including using infusions or gene delivery of GDNF or the related growth factor, neurturin (NRTN). Initial studies, some of which were open label, suggested that this approach could be of value in PD when the agent was injected into the putamen rather than the cerebral ventricles. In subsequent double-blind, placebo-controlled trials, the most recent reporting in 2019, treatment with GDNF did not achieve its primary end point. As a result, there has been uncertainty as to whether GDNF (and by extrapolation, related GDNF family neurotrophic factors) has merit in the future treatment of PD. To critically appraise the existing work and its future, a special workshop was held to discuss and debate this issue. This paper is a summary of that meeting with recommendations on whether there is a future for this therapeutic approach and also what any future PD trial involving GDNF and other GDNF family neurotrophic factors should consider in its design.

摘要

多年来,人们一直致力于通过生长因子修复大脑的概念,包括主要针对帕金森病 (PD) 的各种神经退行性疾病。使用胶质细胞系衍生的神经营养因子 (GDNF)。这种神经营养因子于 1993 年被发现,具有选择性地促进某些神经元群体(包括多巴胺能黑质纹状体通路)存活和再生的作用。这些观察结果导致了一系列 PD 患者的临床试验,包括使用 GDNF 或相关生长因子神经调节蛋白 (NRTN) 的输注或基因传递。最初的一些研究是开放标签的,表明当药物注入壳核而不是侧脑室时,这种方法对 PD 可能有价值。在随后的双盲、安慰剂对照试验中,最近的报告是在 2019 年,GDNF 治疗并未达到其主要终点。因此,对于 GDNF(以及推断的相关 GDNF 家族神经营养因子)在 PD 未来治疗中的价值存在不确定性。为了批判性地评估现有工作及其未来,举办了一次特别研讨会来讨论和辩论这个问题。本文是对该会议的总结,提出了关于这种治疗方法是否有未来的建议,以及任何涉及 GDNF 和其他 GDNF 家族神经营养因子的未来 PD 试验在设计中应考虑的因素。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f0ec/7458523/c7f1953fca22/jpd-10-jpd202004-g001.jpg

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