Antiseizure therapy attenuates cognitive decline in Alzheimer’s disease: A retrospective cohort study

医学 倾向得分匹配 认知功能衰退 认知 回顾性队列研究 内科学 亚临床感染 队列研究 共病 痴呆 物理疗法 队列 认知障碍 癫痫 睡眠剥夺对认知功能的影响 疾病 前瞻性队列研究 药物治疗 神经心理学 小型精神状态检查
作者
Katsunori Yokoi,Masashi Tsujimoto,Keisuke Suzuki,Akinori Takeda,Kentaro Horibe,Eriko Imai,Kazunori Imai,Nao Hatakeyama,Eriko OKADA,Akinori Nakamura,Masahisa Katsuno,Yutaka Arahata
出处
期刊:Journal of Alzheimer's Disease [IOS Press]
卷期号:110 (1): 227-241
标识
DOI:10.1177/13872877251414147
摘要

BackgroundEpileptic seizures and subclinical epileptiform activity are increasingly recognized as comorbidities in Alzheimer's disease (AD) and have been associated with accelerated cognitive decline. Whether antiseizure medication (ASM) therapy favorably influences cognitive trajectories in AD remains unclear.ObjectiveTo assess the effects of ASM therapy on cognitive trajectories in patients with AD with comorbid epilepsy, and to identify patient subgroups most likely to benefit.MethodsWe retrospectively studied 538 patients (403 AD only; 135 AD with comorbid epilepsy) treated with newer-generation ASMs between 2020 and 2025. Cognitive change over 24 months was assessed using the Mini-Mental State Examination (MMSE). Analyses included linear mixed-effects modeling, sliding window interaction analysis across baseline MMSE scores (11-29), and 1:1 propensity score matching stratified by baseline MMSE (≤21, 22-26, and ≥27).ResultsAfter propensity score matching, baseline MMSE scores were well balanced between the groups. The sliding window analysis suggested a subgroup-specific interaction between group and time in the MMSE (range 22-26), peaking at MMSE 25. In the 22-26 stratum, MMSE at 12 months was higher in the AD with comorbid epilepsy group than in the AD-only group (23.23 ± 0.46 versus 20.33 ± 0.52, p < 0.001). The 24-month difference (22.92 ± 1.37 versus 19.36 ± 0.99, p = 0.047) was borderline and considered exploratory.ConclusionsAntiseizure therapy was associated with favorable cognitive trajectories in patients with AD and comorbid epilepsy, particularly with baseline MMSE 22-26. These exploratory findings suggest a potential therapeutic window that warrants confirmation in prospective studies.
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