Djukic Aleksandra, Holtzer Roee, Shinnar Shlomo, Muzumdar Hiren, Rose Susan A, Mowrey Wenzhu, Galanopoulou Aristea S, Shinnar Ruth, Jankowski Jeffrey J, Feldman Judith F, Pillai Sophia, Moshé Solomon L
Saul R. Korey Department of Neurology, Albert Einstein College of Medicine, Bronx, New York; Rett Syndrome Center, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York; Department of Pediatrics, Montefiore Medical Center, Albert Einstein College of Medicine, Bronx, New York.
Saul R. Korey Department of Neurology, Albert Einstein College of Medicine, Bronx, New York; Ferkauf Graduate School of Psychology of Yeshiva University, Bronx, New York.
Pediatr Neurol. 2016 Aug;61:51-7. doi: 10.1016/j.pediatrneurol.2016.05.010. Epub 2016 May 27.
Rett syndrome (RTT) is a severe neurological disease that primarily affects females. The level of brain derived neurotropic factor (BDNF) expression directly correlates with the severity of RTT related symptoms. Because Glatiramer acetate (GA) stimulates secretion of BDNF in the brain, we conducted the study with the objective to assess its efficacy in improving gait velocity cognition, respiratory function, electroencephalographic findings, and quality of life in patients with RTT.
Phase two, open label, single center trial.
ambulatory girls with genetically confirmed RTT, 10 years or older. Pre- and post-treatment measures were compared using the non-parametric Wilcoxon signed rank sum test and paired t-tests.
Ten patients were enrolled and completed the trial. Gait velocity improved significantly (improvement range 13%-95%, p=0.03 for both tests) and emerged as an especially valuable outcome measure with excellent test- retest reliability of the 2 trials within sessions (intraclass correlation coefficient=0.94). Memory, and the breath holding index also improved significantly (p≤0.03). Epileptiform discharges decreased in all four patients who had them at baseline. There was a trend towards improved quality of life, which did not reach statistical significance.
This prospective open-label trial provides important preliminary information related to the efficacy of GA in improving gait velocity in female patients with RTT who are 10 years or older. The results of this trial justify the need for larger scale controlled trials of GA as well as provide a template for assessing the efficacy of other interventions in RTT.
雷特综合征(RTT)是一种主要影响女性的严重神经疾病。脑源性神经营养因子(BDNF)的表达水平与RTT相关症状的严重程度直接相关。由于醋酸格拉替雷(GA)可刺激大脑中BDNF的分泌,我们开展了本研究,旨在评估其对改善10岁及以上RTT患者的步态速度、认知、呼吸功能、脑电图结果和生活质量的疗效。
二期、开放标签、单中心试验。
基因确诊为RTT的能行走的10岁及以上女孩。使用非参数Wilcoxon符号秩和检验和配对t检验比较治疗前后的测量结果。
10名患者入组并完成试验。步态速度显著提高(改善范围为13%-95%,两项测试的p值均为0.03),并且成为一项特别有价值的结果指标,两次试验在疗程内的重测信度极佳(组内相关系数=0.94)。记忆力和屏气指数也显著改善(p≤0.03)。所有4名基线时有癫痫样放电的患者,其癫痫样放电均减少。生活质量有改善趋势,但未达到统计学意义。
这项前瞻性开放标签试验提供了与GA改善10岁及以上女性RTT患者步态速度的疗效相关的重要初步信息。本试验结果证明有必要对GA进行更大规模的对照试验,并为评估RTT中其他干预措施的疗效提供了模板。