Publication

2014 Epilepsy Benchmarks Area II: Prevent Epilepsy and Its Progression

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Last modified
  • 05/21/2025
Type of Material
Authors
    Aristea S , Galanopoulou, Albert Einstein College of MedicineMichael Wong, Washington UniversityDevin Binder, University of California RiversideAdam L. Hartman, Johns Hopkins UniversityElizabeth M. Powell, University of MarylandAvtar Roopra, University of WisconsinRichard Staba, University of California Los AngelesAnnamaria Vezzani, IRCCS Istituto di Ricerche Farmacologiche Mario NegriBrandy Fureman, National Institute of Neurological Disorders and StrokeRaymond Dingledine, Emory University
Language
  • English
Date
  • 2016-05-01
Publisher
  • American Epilepsy Society
Publication Version
Copyright Statement
  • © American Epilepsy Society 2016
Final Published Version (URL)
Title of Journal or Parent Work
Volume
  • 16
Issue
  • 3
Start Page
  • 187
End Page
  • 191
Grant/Funding Information
  • None declared
Abstract
  • The prevention of epilepsy and its progression after initial diagnosis represents one of the most challenging goals of epilepsy research (1). Although epilepsy diagnoses lack a formal component of disease stage, anecdotal clinical observation suggests that individual patients usually fall into one of at least three types of presentation: an easily treated type that is responsive to the first or second antiseizure medications tried, a relapsing/remitting type in which seizure control is intermittent, and a drug-resistant type in which the patient never achieves seizure control with medication (2). As drug-resistant epilepsy is extremely difficult to treat, the successful prevention of epilepsy in at-risk patients may provide the best strategy to alleviate the negative impact of epilepsy. Benchmark II aims to establish therapeutic approaches for preventing the development and progression of epilepsy by 1) understanding epileptogenic processes related to genetic or neurodevelopmental causes, 2) understanding epileptogenic processes related to acquired brain injuries, 3) identifying biomarkers for monitoring epileptogenesis, 4) developing models closely aligned with etiologies of human epilepsies, and 5) identifying molecular targets that drive epileptogenesis or are opposed to it.
Author Notes
  • Correspondence: Brandy Fureman, PhD, Current address: Epilepsy Foundation of America, 8301 Professional Place, Landover, MD. E-mail: bfureman@efa.org
Keywords
Research Categories
  • Engineering, Biomedical
  • Health Sciences, Pharmacology
  • Biology, Neuroscience

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