Clinical Biomarkers and Prediction Models for Poststroke Epilepsy: Have We Settled the Scores Yet?

Neurol Clin Pract

Department of Neurology (ASY, JFM, AMF), Mayo Clinic, Jacksonville, FL.

Published: April 2023

AI Article Synopsis

  • The increasing success of reperfusion therapies for stroke has led to a larger population at risk for poststroke epilepsy (PSE), but there's currently no evidence supporting the use of preventative antiseizure medication.
  • Recent research indicates a complex relationship between stroke, PSE, and dementia, but existing predictive models are not well-validated for effective risk stratification.
  • Future studies utilizing advancements in genetics, imaging, and artificial intelligence may uncover new biomarkers and treatment strategies to better manage high-risk patients and break the cycle of stroke-related complications.

Article Abstract

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.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC10022724PMC
http://dx.doi.org/10.1212/CPJ.0000000000200146DOI Listing

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