Current and Emerging Precision Therapies for Developmental and Epileptic Encephalopathies.

Journal: Pediatric neurology
Published Date:

Abstract

Developmental and epileptic encephalopathies (DEEs) are severe neurological disorders characterized by childhood-onset seizures and significant developmental impairments. Seizures are often refractory to treatment with traditional antiseizure medications, which fail to address the underlying genetic and molecular mechanisms. This comprehensive review explores the evolving landscape of precision therapeutics for DEEs, focusing on mechanism-driven interventions across key pathophysiologic categories. Targeted approaches for channelopathies include antisense oligonucleotides and gene therapies, such as zorevunersen and ETX101 for SCN1A-related Dravet syndrome, alongside novel small molecules for other ion channel disorders. Advances in targeting neurotransmitter receptor dysfunctions, including γ-aminobutyric acid and glutamate receptor variants, highlight the use of modulators such as gaboxadol, radiprodil, and l-serine, alongside emerging gene therapies. For synaptic dysfunctions, innovative treatments such as chemical chaperones for STXBP1-related disorders and Ras-Raf-MEK-ERK inhibitors for SYNGAP1 pathologies are discussed. The review also examines precision interventions targeting cellular signaling pathways in tuberous sclerosis complex, epigenetic regulation in Rett syndrome, and metabolic interventions like ketogenic diets and targeted supplementation for specific genetic etiologies. Additionally, the importance of enhancing access to genetic testing, conducting robust natural history studies, and employing innovative clinical trial designs is emphasized. Future directions focus on addressing the challenges in developing and implementing gene-based therapies, integrating systems biology, leveraging artificial intelligence for data analysis, and fostering collaboration among stakeholders. The rapidly advancing field of precision therapeutics for DEEs holds promise to improve outcomes through tailored, equitable, and patient-centered care.

Authors

  • Debopam Samanta
    Division of Child Neurology, Department of Pediatrics, University of Arkansas for Medical Sciences, Little Rock, Arkansas. Electronic address: dsamanta@uams.edu.
  • Sonal Bhatia
    Department of Neurology, Medical University of South Carolina, Charleston, South Carolina.
  • Senyene E Hunter
    Division of Child Neurology, Department of Neurology, University of North Carolina at Chapel Hill, Chapel Hill, North Carolina.
  • Chethan K Rao
    Division of Pediatric Neurology, Department of Pediatrics, University of Maryland, Baltimore, Maryland.
  • Katherine Xiong
    Division of Pediatric Neurology, Department of Neurology, Stanford School of Medicine, Palo Alto, California.
  • Cemal Karakas
    Division of Pediatric Neurology, Department of Pediatrics, University of Louisville, Louisville, Kentucky.
  • Puck C Reeders
    Brain Institute, Nicklaus Children's Hospital, Miami, Florida.
  • Gozde Erdemir
    Division of Child Neurology, Department of Pediatrics, Penn State Health Children's Hospital, Penn State College of Medicine, Hershey, Pennsylvania.
  • Shifteh Sattar
    Division of Child Neurology, Department of Neurosciences, Rady Children's Hospital & University of California, San Diego, California.
  • Erika Axeen
    Division of Child Neurology, Department of Neurology, University of Virginia School of Medicine, Charlottesville, Virginia.
  • Amanda G Sandoval Karamian
    Division of Pediatric Neurology, Department of Pediatrics, University of Utah School of Medicine and Primary Children's Hospital, Salt Lake City, Utah.
  • Anthony L Fine
    Divisions of Child and Adolescent Neurology and Epilepsy, Department of Neurology, Mayo Clinic, Rochester, Minnesota.
  • Cynthia G Keator
    Department of Neurology, Jane and John Institute of Mind Health, Cook Children's Hospital, Fort Worth, Texas.
  • Danielle Nolan
    Division of Pediatric Neurology, Corewell Health East Beaumont Children's, Royal Oak, Michigan.
  • John M Schreiber
    Division of Epilepsy, Clinical Neurophysiology, and Critical Care Neurology, Children's National Hospital, Washington, District of Columbia.