Florida Department of Neurology, Mayo Clinic, Jacksonville, Florida, USA.
Florida Department of Biostatistics, Mayo Clinic, Jacksonville, Florida, USA.
Muscle Nerve. 2021 Aug;64(2):215-219. doi: 10.1002/mus.27328. Epub 2021 May 27.
INTRODUCTION/AIMS: Cortical hyperexcitability is a feature of amyotrophic lateral sclerosis (ALS) and cortical excitability can be measured using transcranial magnetic stimulation (TMS). Resting motor threshold (MT) is a measure of cortical excitability, largely driven by glutamate. Perampanel, a glutamate α-amino-3-hydroxy-5-methyl-4-isoxazolepropionic acid (AMPA) receptor blocker, is predicted to increase the cortical excitability threshold. This study aimed to evaluate TMS to functionally assess target engagement in a study of perampanel in ALS.
We studied the MT of ALS patients randomized to a single dose of perampanel or placebo 5:1 hourly for 4 h. Twelve patients participated at 4 mg and 7 returned for dosing and retesting at 8 mg. The study was terminated in April 2020 due to coronavirus disease 2019-related restrictions, after 7 out of 12 planned patients had received the 8 mg dose. Serum concentrations were also measured.
Ten patients received the 4 mg dose (2 received placebo) and 5 received the 8 mg dose (2 received placebo). Motor Threshold increased at 2 h after dosing in the combined treatment group +7% of maximal stimulator output (P < .01). Change could be detected in the larger 4 mg group (P = .02), but not in the smaller 8 mg dose group (P = .1). No side effects were reported after single dose exposure.
This study shows that perampanel effects the physiology of upper motor neurons. Studies aiming at gauging the effect of perampanel on ALS disease progression are already ongoing. Motor threshold may serve as a marker of biological target engagement.
介绍/目的:皮质兴奋性过高是肌萎缩侧索硬化症(ALS)的特征,皮质兴奋性可以通过经颅磁刺激(TMS)来测量。静息运动阈值(MT)是皮质兴奋性的一种测量方法,主要受谷氨酸驱动。培拉西坦,一种谷氨酸α-氨基-3-羟基-5-甲基-4-异恶唑丙酸(AMPA)受体阻滞剂,预计会增加皮质兴奋性阈值。本研究旨在通过培拉西坦治疗 ALS 的研究,评估 TMS 来功能性评估其靶标结合。
我们研究了随机接受培拉西坦或安慰剂单剂量 5:1 小时 4 小时的 ALS 患者的 MT。12 名患者接受了 4mg 治疗,其中 7 名患者返回接受 8mg 剂量的治疗和重新测试。由于与 2019 年冠状病毒病相关的限制,该研究于 2020 年 4 月终止,在计划的 12 名患者中有 7 名接受了 8mg 剂量。还测量了血清浓度。
10 名患者接受了 4mg 剂量(2 名接受安慰剂),5 名接受了 8mg 剂量(2 名接受安慰剂)。在联合治疗组中,给药后 2 小时 MT 增加了 7%最大刺激器输出(P<.01)。较大的 4mg 组可以检测到变化(P=0.02),但较小的 8mg 剂量组则没有(P=0.1)。单次暴露后无不良反应报告。
本研究表明,培拉西坦影响上运动神经元的生理学。旨在评估培拉西坦对 ALS 疾病进展影响的研究已经在进行中。运动阈值可能是生物靶标结合的标志物。