Safety, tolerability, and efficacy outcomes of the Investigation of Levetiracetam in Alzheimer's disease (ILiAD) study: a pilot, double-blind placebo-controlled crossover trial

IF 2.8 3区 医学 Q2 CLINICAL NEUROLOGY
Epilepsia Open Pub Date : 2024-10-14 DOI:10.1002/epi4.13070
Arjune Sen, Sofia Toniolo, Xin You Tai, Mary Akinola, Mkael Symmonds, Sergio Mura, Joanne Galloway, Angela Hallam, Jane Y. C. Chan, Ivan Koychev, Chris Butler, John Geddes, Gabriel Davis Jones, Younes Tabi, Raquel Maio, Eleni Frangou, Sharon Love, Sian Thompson, Rohan Van Der Putt, Sanjay G. Manohar, Rupert McShane, Masud Husain
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引用次数: 0

Abstract

Objective

To assess whether the antiseizure medication levetiracetam may improve cognition in individuals with Alzheimer's disease who have not previously experienced a seizure.

Methods

We performed a randomized, double-blind, placebo-controlled crossover pilot study in individuals with mild-to-moderate Alzheimer's disease. Electroencephalography was performed at baseline and those with active epileptiform discharges were excluded. Eligible participants were randomized to placebo for 12 weeks or an active arm of oral levetiracetam (4 weeks up-titration to levetiracetam 500 mg twice daily, 4 weeks maintained on this dose followed by 4 weeks down-titration to nil). Participants then crossed over to the other arm. The primary outcome was change in cognitive function assessed by the Oxford Memory Task, a task sensitive to hippocampal memory binding. Secondary outcomes included tolerability, other neuropsychological scales, and general questionnaires.

Results

Recruitment numbers were severely limited owing to restrictions from the COVID-19 pandemic at the time of the study. Eight participants completed both arms of the study (mean age 68.4 years [SD = 9.2]; 5 females [62.5%]). No participants withdrew from the study and there was no significant difference between reported side effects in the active levetiracetam or placebo arm. Measures of mood and quality of life were also not significantly different between the two arms based on participant or carer reports. In limited data analysis, there was no statistically significant difference between participants in the active levetiracetam and placebo arm on the memory task.

Significance

This pilot study demonstrates that levetiracetam was well tolerated in individuals with Alzheimer's disease who do not have a history of seizures and has no detrimental effect on mood or quality of life. Larger studies are needed to assess whether levetiracetam may have a positive effect on cognitive function in subsets of individuals with Alzheimer's disease.

Plain Language Summary

Abnormal electrical activity within the brain, such as is seen in seizures, might contribute to memory problems in people with dementia. We completed a clinical trial to see if an antiseizure medication, levetiracetam, could help with memory difficulties in people with Alzheimer's disease (the most common cause of dementia). In this pilot study, we could not prove whether levetiracetam helped memory function. We did show that the drug is safe and well tolerated in people with dementia who have not had a seizure. This work, therefore, offers a platform for future research exploring antiseizure medications in people with dementia.

Abstract Image

左乙拉西坦治疗阿尔茨海默病(ILiAD)研究的安全性、耐受性和疗效结果:双盲安慰剂对照交叉试验。
目的评估抗癫痫药物左乙拉西坦能否改善以前未经历过癫痫发作的阿尔茨海默病患者的认知能力:我们在轻度至中度阿尔茨海默病患者中开展了一项随机、双盲、安慰剂对照交叉试验研究。在基线时进行脑电图检查,并排除癫痫样放电活跃者。符合条件的参与者被随机分配到安慰剂组,为期12周;或口服左乙拉西坦的活性组(上调剂量至左乙拉西坦500毫克,每日两次,为期4周;维持此剂量4周后,下调剂量至零)。然后,参与者交叉接受另一组治疗。主要结果是通过牛津记忆任务评估认知功能的变化,这是一项对海马记忆结合敏感的任务。次要结果包括耐受性、其他神经心理学量表和一般问卷调查:由于研究时COVID-19大流行的限制,招募人数受到严重限制。八名参与者完成了两臂研究(平均年龄 68.4 岁 [SD = 9.2];五名女性 [62.5%])。没有参与者退出研究,而且左乙拉西坦活性组和安慰剂组报告的副作用没有明显差异。根据参与者或照护者的报告,两组患者的情绪和生活质量也无明显差异。在有限的数据分析中,左乙拉西坦活性组和安慰剂组的参与者在记忆任务上没有显著的统计学差异:这项试验性研究表明,没有癫痫发作史的阿尔茨海默病患者对左乙拉西坦的耐受性良好,而且对情绪或生活质量没有不利影响。我们需要进行更大规模的研究,以评估左乙拉西坦是否会对阿尔茨海默氏症亚群患者的认知功能产生积极影响。我们完成了一项临床试验,以了解抗癫痫药物左乙拉西坦是否有助于阿尔茨海默氏症(最常见的痴呆症病因)患者的记忆障碍。在这项试验研究中,我们无法证明左乙拉西坦是否有助于记忆功能。但我们确实证明,这种药物对没有发作过的痴呆症患者是安全的,而且耐受性良好。因此,这项研究为今后探索抗癫痫药物在痴呆症患者中的应用提供了一个平台。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Epilepsia Open
Epilepsia Open Medicine-Neurology (clinical)
CiteScore
4.40
自引率
6.70%
发文量
104
审稿时长
8 weeks
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