Wayne State University School of Medicine, Parkinson's Disease and Movement Disorders Program, Henry Ford West Bloomfield Hospital, MI, USA.
Lancet Neurol. 2011 Apr;10(4):309-19. doi: 10.1016/S1474-4422(11)70039-4.
BACKGROUND: Gene transfer of glutamic acid decarboxylase (GAD) and other methods that modulate production of GABA in the subthalamic nucleus improve basal ganglia function in parkinsonism in animal models. We aimed to assess the effect of bilateral delivery of AAV2-GAD in the subthalamic nucleus compared with sham surgery in patients with advanced Parkinson's disease. METHODS: Patients aged 30-75 years who had progressive levodopa-responsive Parkinson's disease and an overnight off-medication unified Parkinson's disease rating scale (UPDRS) motor score of 25 or more were enrolled into this double-blind, phase 2, randomised controlled trial, which took place at seven centres in the USA between Nov 17, 2008, and May 11, 2010. Infusion failure or catheter tip location beyond a predefined target zone led to exclusion of patients before unmasking for the efficacy analysis. The primary outcome measure was the 6-month change from baseline in double-blind assessment of off-medication UPDRS motor scores. This trial is registered with ClinicalTrials.gov, NCT00643890. FINDINGS: Of 66 patients assessed for eligibility, 23 were randomly assigned to sham surgery and 22 to AAV2-GAD infusions; of those, 21 and 16, respectively, were analysed. At the 6-month endpoint, UPDRS score for the AAV2-GAD group decreased by 8·1 points (SD 1·7, 23·1%; p<0·0001) and by 4·7 points in the sham group (1·5, 12·7%; p=0·003). The AAV2-GAD group showed a significantly greater improvement from baseline in UPDRS scores compared with the sham group over the 6-month course of the study (RMANOVA, p=0·04). One serious adverse event occurred within 6 months of surgery; this case of bowel obstruction occurred in the AAV2-GAD group, was not attributed to treatment or the surgical procedure, and fully resolved. Other adverse events were mild or moderate, likely related to surgery and resolved; the most common were headache (seven patients in the AAV2-GAD group vs two in the sham group) and nausea (six vs two). INTERPRETATION: The efficacy and safety of bilateral infusion of AAV2-GAD in the subthalamic nucleus supports its further development for Parkinson's disease and shows the promise for gene therapy for neurological disorders. FUNDING: Neurologix.
背景:谷氨酸脱羧酶(GAD)的基因转移和其他调节丘脑下核中 GABA 产生的方法改善了帕金森病动物模型中的基底节功能。我们旨在评估与假手术相比,双侧立体定向丘脑下核内 AAV2-GAD 传递在晚期帕金森病患者中的效果。
方法:我们招募了年龄在 30-75 岁之间的患者,这些患者患有进行性左旋多巴反应性帕金森病,且在停止用药一夜后,统一帕金森病评定量表(UPDRS)运动评分达到 25 分或以上。这项双盲、2 期、随机对照试验于 2008 年 11 月 17 日至 2010 年 5 月 11 日在美国的 7 个中心进行。输注失败或导管尖端位置超出预定目标区域,导致在未揭盲进行疗效分析之前排除患者。主要观察指标是在 6 个月时,从基线评估的、停止用药的 UPDRS 运动评分的变化。这项试验在 ClinicalTrials.gov 注册,编号为 NCT00643890。
结果:在评估合格性的 66 名患者中,23 名被随机分配至假手术组,22 名被分配至 AAV2-GAD 输注组;分别有 21 名和 16 名患者被纳入分析。在 6 个月的研究终点时,AAV2-GAD 组的 UPDRS 评分下降了 8.1 分(标准差 1.7,23.1%;p<0.0001),而假手术组下降了 4.7 分(1.5,12.7%;p=0.003)。与假手术组相比,AAV2-GAD 组在 6 个月的研究过程中,UPDRS 评分的改善有显著的统计学意义(重复测量方差分析,p=0.04)。术后 6 个月内发生了 1 例严重不良事件;这例肠阻塞发生在 AAV2-GAD 组,与治疗或手术过程无关,完全缓解。其他不良事件为轻度或中度,可能与手术相关并已缓解;最常见的是头痛(AAV2-GAD 组 7 例,假手术组 2 例)和恶心(6 例 vs 2 例)。
解释:双侧立体定向丘脑下核内 AAV2-GAD 输注的疗效和安全性支持其在帕金森病中的进一步发展,并为神经障碍的基因治疗带来了希望。
资金来源:Neurologix。
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