TRANscranial direct current stimulation for FOcal Refractory epilepsy in mitochondrial disease (TRANSFORM): delayed-start, randomised, double-blinded, placebo-controlled study.

IF 2.2 3区 医学 Q3 CLINICAL NEUROLOGY BMC Neurology Pub Date : 2024-10-22 DOI:10.1186/s12883-024-03907-6
Katrin A Bangel, Albert Z Lim, Alasdair Blain, Yi Shiau Ng, Amy Winder, Joseph Bulmer, Grainne Gorman, Mark Baker, Robert McFarland
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Abstract

Background: Focal epilepsy is common in children and adults with mitochondrial disease. Seizures are often refractory to pharmacological treatment and, in this patient group, frequently evolve to refractory focal status epilepticus (also known as epilepsia partialis continua). Where this occurs, the long-term prognosis is poor. Transcranial DC stimulation (tDCS) is a promising, non-invasive, adjunctive treatment alternative to common surgical procedures. Limited recruitment of study participants with this rare disease and the ethical challenges of administering a treatment to one group and not another, while maintaining strict methodological rigour can pose challenges to the design of a clinical study.

Method: We designed the first delayed start, double-blinded, sham-controlled study to evaluate the efficacy of tDCS as an adjunctive treatment for focal epilepsy. We will include participants with a genetically confirmed diagnosis of mitochondrial disease with drug-resistant focal epilepsy aged ≥ 2 years, aiming to collect 30 episodes of focal status epilepticus, each treated for a maximum period of 14 days. The early start intervention arm will receive tDCS from day 1. The delayed start intervention arm will receive sham stimulation until crossover on day 3. Our primary endpoint is a greater than 50% reduction from baseline (on day 0) in seizure frequency assessed by 3x daily reporting, accelerometery, and video monitoring. Changes in the underlying epileptogenic focus within the brain related to the tDCS intervention will be assessed by magnetic resonance imaging (MRI) and/or electroencephalography (EEG).

Discussion: Study results in favour of treatment efficacy would support development of tDCS into a mainstream treatment option for focal epileptic seizures related to mitochondrial disease.

Trials registration: ISRCTN: 18,241,112; registered on 16/11/2021.

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治疗线粒体病难治性癫痫的经颅直流电刺激(TRANSFORM):延迟启动、随机、双盲、安慰剂对照研究。
背景:局灶性癫痫常见于患有线粒体疾病的儿童和成人。癫痫发作常常对药物治疗产生耐药性,在这类患者中,经常演变为难治性局灶性癫痫(也称为癫痫部分性持续状态)。如果出现这种情况,长期预后很差。经颅直流电刺激(tDCS)是一种很有前景的非侵入性辅助治疗方法,可替代常见的外科手术。但招募到的患有这种罕见疾病的研究人员有限,而且在保持严格的方法学严谨性的同时,还要对一组人而不是另一组人进行治疗,这些伦理挑战都给临床研究的设计带来了挑战:我们设计了首个延迟开始、双盲、假对照研究,以评估 tDCS 作为局灶性癫痫辅助治疗方法的疗效。我们将纳入经基因确诊患有线粒体疾病并伴有耐药性局灶性癫痫且年龄≥2岁的参与者,旨在收集30次局灶性癫痫发作,每次治疗时间最长为14天。早期干预组将从第 1 天开始接受 tDCS 治疗。延迟开始干预组将接受假刺激,直到第 3 天交叉。我们的主要终点是通过每日 3 次报告、加速度计和视频监控评估癫痫发作频率比基线(第 0 天)减少 50% 以上。脑内与 tDCS 干预相关的潜在致痫灶的变化将通过磁共振成像(MRI)和/或脑电图(EEG)进行评估:讨论:有利于治疗效果的研究结果将支持将 tDCS 发展成为线粒体疾病相关局灶性癫痫发作的主流治疗方案:ISRCTN:18,241,112;注册日期:2021年11月16日。
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来源期刊
BMC Neurology
BMC Neurology 医学-临床神经学
CiteScore
4.20
自引率
0.00%
发文量
428
审稿时长
3-8 weeks
期刊介绍: BMC Neurology is an open access, peer-reviewed journal that considers articles on all aspects of the prevention, diagnosis and management of neurological disorders, as well as related molecular genetics, pathophysiology, and epidemiology.
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