Yonas Amen S, Meschia James F, Feyissa Anteneh M
Department of Neurology (ASY, JFM, AMF), Mayo Clinic, Jacksonville, FL.
Neurol Clin Pract. 2023 Apr;13(2):e200146. doi: 10.1212/CPJ.0000000000200146. Epub 2023 Mar 14.
In an era of time-dependent reperfusion and recanalization therapy for stroke leading to improved survival, there is a growing population at risk of poststroke epilepsy (PSE). Accumulating evidence suggests a multidirectional interaction among stroke, PSE, and dementia in stroke survivors. There is no evidence to justify prophylactic antiseizure medication (ASM) to reduce these morbidities. Although several predictive molecular biomarkers and scoring models have been proposed, they remain inadequately validated for stratifying risk and indicating who will benefit from prophylactic ASM. Studies leveraging advances in genetics, metabolomics, electrophysiology, imaging, and artificial intelligence (AI) may help to discover noninvasive molecular biomarkers and easy-to-score models. These discoveries should improve our understanding of epileptogenesis in PSE and identify new pharmacologic targets. Besides, accurately identifying high-risk patients and timely initiating prophylactic ASM therapy has the potential to disrupt the feed-forward multidirectional interaction among stroke, PSE, and dementia.
在一个因中风的时间依赖性再灌注和再通治疗而使生存率提高的时代,中风后癫痫(PSE)的风险人群正在增加。越来越多的证据表明,中风幸存者中中风、PSE和痴呆之间存在多向相互作用。没有证据证明预防性抗癫痫药物(ASM)能降低这些发病率。尽管已经提出了几种预测性分子生物标志物和评分模型,但它们在分层风险和指出谁将从预防性ASM中获益方面仍未得到充分验证。利用遗传学、代谢组学、电生理学、影像学和人工智能(AI)方面的进展进行的研究可能有助于发现非侵入性分子生物标志物和易于评分的模型。这些发现应能增进我们对PSE中癫痫发生的理解,并确定新的药理学靶点。此外,准确识别高危患者并及时启动预防性ASM治疗有可能打破中风、PSE和痴呆之间的前馈多向相互作用。