Orphanet Journal of Rare Diseases (Jan 2023)

Neurophysiological assessment of cortical activity in DEPDC5- and NPRL3-related epileptic mTORopathies

  • Madora Mabika,
  • Kristian Agbogba,
  • Samantha Côté,
  • Sarah Lippé,
  • Émilie Riou,
  • Cécile Cieuta,
  • Jean-François Lepage

DOI
https://doi.org/10.1186/s13023-022-02600-6
Journal volume & issue
Vol. 18, no. 1
pp. 1 – 15

Abstract

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Abstract Background Mutations in the GATOR1 complex genes, DEPDC5 and NPRL3, play a major role in the development of lesional and non-lesional focal epilepsy through increased mTORC1 signalling. We aimed to assess the effects of mTORC1 hyperactivation on GABAergic inhibitory circuits, in 3 and 5 individuals carrying DEPDC5 and NPRL3 mutations respectively using a multimodal approach including transcranial magnetic stimulation (TMS), magnetic resonance spectroscopy (MRS), and electroencephalography (EEG). Results Inhibitory functions probed by TMS and MRS showed no effect of mutations on cortical GABAergic receptor-mediated inhibition and GABA concentration, in both cortical and subcortical regions. However, stronger EEG theta oscillations and stronger and more synchronous gamma oscillations were observed in DEPDC5 and NPRL3 mutations carriers. Conclusions These results suggest that DEPDC5 and NPRL3-related epileptic mTORopathies may not directly modulate GABAergic functions but are nonetheless characterized by a stronger neural entrainment that may be reflective of a cortical hyperexcitability mediated by increased mTORC1 signaling.

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