Abnormal Brain Gamma Oscillations in Response to Auditory Stimulation in Dravet Syndrome
Rocio Sanchez-Carpintero (1), Elena Urrestarazu (2), Sofía Cieza (3), Manuel Alegre (2), Julio Artieda (2), Nerea Crespo-Eguilaz (4), Miguel Valencia (5)
(1) Pediatric Neurology Unit. Department of Pediatrics. Clínica Universidad de Navarra, Pamplona, Spain; IdiSNA, Navarra Institute for Health Research, Pamplona, Spain.
(2) IdiSNA, Navarra Institute for Health Research, Pamplona, Spain; Neurophysiology Department, Clínica Universidad de Navarra, Universidad de Navarra, Pamplona, Spain.
(3) Neurophysiology Department, Clínica Universidad de Navarra, Universidad de Navarra, Pamplona, Spain.
(4) Pediatric Neurology Unit. Department of Pediatrics. Clínica Universidad de Navarra, Pamplona, Spain.
(5) IdiSNA, Navarra Institute for Health Research, Pamplona, Spain; University of Navarra, Neuroscience Program, CIMA, Pamplona, Spain.
To evaluate the capability of children with Dravet syndrome to generate brain γ-oscillatory activity in response to auditory steady-state stimulation.
Fifty-one subjects were included: 13 with Dravet syndrome with SCN1A gene alterations, 26 with non-Dravet epilepsies and 12 healthy controls. Responses to auditory steady-state stimulation elicited with a chirp-modulated tone between 1 and 120 Hz were collected in subjects and compared across groups.
Subjects with Dravet syndrome showed weak or no responses in the 1-120 Hz frequency range. Healthy controls showed oscillatory responses following the frequency of the modulation that were maximal in the low (30-70 Hz) and high (80-120) γ-ranges both, in the power and inter-trial coherence estimates. Non-Dravet epileptic children showed differences in the auditory responses when compared with the healthy controls but were able to generate oscillatory evoked activities following the frequency-varying stimulation.
The ability to generate brain γ-oscillatory activity of children with Dravet in response to a chirp-modulated auditory stimulus is highly impaired, is not due to epilepsy and is consistent with the Nav1.1 channel dysfunction affecting interneuron activity seen in Dravet mouse models.
The reported deficits in the brain oscillatory activity evoked by chirp modulated tones in children with Dravet is compatible with Dravet syndrome disease mechanisms and constitutes a potential biomarker for future disease-modifying interventions.
CITA DEL ARTÍCULO Eur J Paediatr Neurol 2020 Jan;24:134-141. doi: 10.1016/j.ejpn.2019.12.004. Epub 2019 Dec 13