Neuromodulation strategies in developmental and epileptic encephalopathies

Epilepsy Behav. 2024 Nov:160:110067. doi: 10.1016/j.yebeh.2024.110067. Epub 2024 Oct 10.

Abstract

Developmental and epileptic encephalopathies (DEEs) are a group of childhood-onset epilepsy syndromes characterized by frequent seizures, severe cognitive and behavioral impairments, and poor long-term outcomes. These conditions are typically refractory to currently available medical therapies, prompting recent exploration of neuromodulation treatments such as deep brain stimulation (DBS) and responsive neurostimulation (RNS), which aim to modulate epileptic networks spanning cortical and subcortical regions. These advances have occurred alongside an improved understanding of syndrome-specific and interictal epileptiform discharge/seizure-specific brain networks. By targeting key nodes within these networks, DBS and RNS hold promise for influencing seizures and associated cognitive and behavioral comorbidities. Initial experiences with centromedian (CM) thalamic DBS for Lennox-Gastaut syndrome (LGS) have shown modest efficacy across multiple seizure types. Reports also indicate the application of DBS and RNS across various genetic and structural etiologies commonly associated with DEEs, with mixed success. Although DBS and RNS are increasingly used in LGS and other DEEs, their mixed efficacy highlights a knowledge gap in understanding why some patients with LGS do not respond and which neuromodulation approach is most effective for other DEEs. To address these issues, this review first discusses recent neuroimaging studies showing similarities and differences in the epileptic brain networks underlying various DEEs, revealing the common involvement of the thalamus and the default-mode network (DMN) across multiple DEEs. We then examine thalamic DBS for LGS to illustrate how such network insights may be used to optimize neuromodulation. Although network-based neuromodulation is still in its infancy, the LGS model may serve as a framework for other DEEs, where optimal treatment necessitates consideration of the underlying epileptic networks. Lastly, the review suggests future research directions, including individualized connectivity assessment and biomarker identification through collaborative efforts, which may enhance the therapeutic potential of neuromodulation for individuals living with DEEs.

Keywords: D/EE-SWAS; Dravet syndrome; Epilepsy of infancy with migrating focal seizures; Epileptic brain networks; FIRES; Hypothalamic hamartoma; Infantile spasms; Myoclonic atonic epilepsy; Ohtahara syndrome; Progressive myoclonus epilepsies; Tuberous sclerosis complex.

Publication types

  • Review

MeSH terms

  • Brain / physiopathology
  • Deep Brain Stimulation* / methods
  • Epilepsy / physiopathology
  • Epilepsy / therapy
  • Humans
  • Lennox Gastaut Syndrome / therapy