Ropper Allan H, Gorson Kenneth C, Gooch Clifton L, Weinberg David H, Pieczek Ann, Ware James H, Kershen Joshua, Rogers Adam, Simovic Drasko, Schratzberger Peter, Kirchmair Rudolf, Losordo Douglas
Department of Neurology, Brigham and Women's Hospital, Boston, MA 02115, USA.
Ann Neurol. 2009 Apr;65(4):386-93. doi: 10.1002/ana.21675.
Randomized, blinded trial of intramuscular gene transfer using plasmid vascular endothelial growth factor (VEGF) to treat diabetic polyneuropathy.
Diabetic patients with polyneuropathy were randomized to receive a VEGF-to-placebo ratio of 3:1. Three sets of injections were given at eight standardized sites adjacent to the sciatic, peroneal, and tibial nerves of one leg. Primary outcomes were change in symptom score at 6 months and a prespecified overall clinical and electrophysiological improvement score. Secondary outcomes were differences in symptoms, examination scores, visual analog pain scale, nerve conduction, and quantitative sensory testing.
Thirty-nine patients received plasmid VEGF and 11 received placebo. Mean symptom score improved in both legs at 6 months, favoring VEGF over placebo (-1.2 +/- 0.5 vs -0.9 +/- 0.5; p < 0.01 after adjustment for change in the untreated leg) and compared with the untreated leg (-0.7 +/- 0.5; p = 0.02). The region of sensory loss and visual analog pain scale improved in the treated group (-1.5 vs -0.5; p = 0.01). Twelve of 39 VEGF versus 2 of 11 placebo patients met criterion for overall improvement. Other measures including nerve conduction potentials did not improve. There were 84 adverse events in VEGF patients, and 22 were serious; there were 51 events in placebo patients, and 2 were serious.
Intramuscular plasmid VEGF gene transfer improved diabetic neuropathic symptoms, meeting primary end-point criteria for efficacy but not affecting most secondary measures. Treatment was associated with more serious adverse events that did not reach statistical significance. These results are not conclusive but may justify further clinical study.
采用质粒血管内皮生长因子(VEGF)进行肌肉内基因转移治疗糖尿病性多发性神经病的随机、双盲试验。
将患有多发性神经病的糖尿病患者随机分组,使接受VEGF与安慰剂的比例为3:1。在一条腿的坐骨神经、腓总神经和胫神经相邻的八个标准化部位进行三组注射。主要结局为6个月时症状评分的变化以及预先设定的总体临床和电生理改善评分。次要结局为症状、检查评分、视觉模拟疼痛量表、神经传导和定量感觉测试方面的差异。
39例患者接受了质粒VEGF,11例接受了安慰剂。6个月时,双腿的平均症状评分均有所改善,VEGF组优于安慰剂组(-1.2±0.5对-0.9±0.5;未经治疗腿的变化调整后p<0.01),且与未经治疗的腿相比也有改善(-0.7±0.5;p = 0.02)。治疗组感觉丧失区域和视觉模拟疼痛量表有所改善(-1.5对-0.5;p = 0.01)。39例接受VEGF治疗的患者中有12例,11例接受安慰剂治疗的患者中有2例达到总体改善标准。包括神经传导电位在内的其他指标未得到改善。接受VEGF治疗的患者发生84起不良事件,其中22起为严重不良事件;接受安慰剂治疗的患者发生51起不良事件,其中2起为严重不良事件。
肌肉内注射质粒VEGF基因转移改善了糖尿病性神经病变症状,达到了疗效的主要终点标准,但未影响大多数次要指标。治疗与更多严重不良事件相关,但未达到统计学显著性。这些结果尚无定论,但可能为进一步的临床研究提供依据。