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Randomized controlled trial of intraputamenal glial cell line–derived neurotrophic factor infusion in Parkinson disease

胶质细胞源性神经生长因子 帕金森病 运动障碍 多巴胺能 医学 随机对照试验 安慰剂 临床终点 神经营养因子 麻醉 壳核 内科学 多巴胺 疾病 病理 受体 替代医学
作者
Anthony E. Lang,Steven Gill,Nikunj K. Patel,Andrés M. Lozano,John G. Nutt,Richard D. Penn,David J. Brooks,Gary Hotton,Elena Moro,Peter Heywood,Matthew Brodsky,Kim J. Burchiel,Patrick J. Kelly,Arif Dalvi,B.L. Scott,Mark Stacy,Dennis A. Turner,Virginia Wooten,W. Jeff Elias,Edward R. Laws,Vijay Dhawan,A. Jon Stoessl,James Matcham,Robert J. Coffey,Michael Traub
出处
期刊:Annals of Neurology [Wiley]
卷期号:59 (3): 459-466 被引量:908
标识
DOI:10.1002/ana.20737
摘要

Abstract Objective Glial cell line–derived neurotrophic factor (GDNF) exerts potent trophic influence on midbrain dopaminergic neurons. This randomized controlled clinical trial was designed to confirm initial clinical benefits observed in a small, open‐label trial using intraputamenal (Ipu) infusion of recombinant human GDNF (liatermin). Methods Thirty‐four PD patients were randomized 1 to 1 to receive bilateral continuous Ipu infusion of liatermin 15μg/putamen/day or placebo. The primary end point was the change in Unified Parkinson Disease Rating Scale (UPDRS) motor score in the practically defined off condition at 6 months. Secondary end points included other UPDRS scores, motor tests, dyskinesia ratings, patient diaries, and 18 F‐dopa uptake. Results At 6 months, mean percentage changes in “off” UPDRS motor score were −10.0% and −4.5% in the liatermin and placebo groups, respectively. This treatment difference was not significant (95% confidence interval, −23.0 to 12.0, p = 0.53). Secondary end point results were similar between the groups. A 32.5% treatment difference favoring liatermin in mean 18 F‐dopa influx constant ( p = 0.019) was observed. Serious, device‐related adverse events required surgical repositioning of catheters in two patients and removal of devices in another. Neutralizing antiliatermin antibodies were detected in three patients (one on‐study and two in the open‐label extension). Interpretation Liatermin did not confer the predetermined level of clinical benefit to patients with PD despite increased 18 F‐dopa uptake. It is uncertain whether technical differences between this trial and positive open‐label studies contributed in any way this negative outcome. Ann Neurol 2006
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