Objective: To examine sleep physiology in children with Dup15q syndrome, with focus on oscillatory power, sleep spindle density and slow wave sleep, and to compare these features to those in typically developing children.
Background: Duplications of 15q11.2-13.1 (Dup15q syndrome) are highly penetrant for intellectual disability, autism, hypotonia and epilepsy. Genes in the 15q region, particularly UBE3A and a cluster of GABAA receptor genes, are critical for neural development, disrupting synaptic protein synthesis and degradation as well as inhibitory neurotransmission. Children with Dup15q syndrome have increased beta oscillations (12–30 Hz) during wakefulness that likely reflect aberrant GABAergic neurotransmission, and studies have shown that non-REM sleep rhythms are also highly dependent on GABAergic neurotransmission. Healthy sleep physiology is necessary for robust cognitive development, yet no studies to date have quantified NREM sleep physiology parameters in children with Dup15q syndrome.
Design/Methods: 7 hours of overnight sleep EEG recording from a cohort of children with Dup15q syndrome (n=15, mean age: 5.7 years) and age-matched neurotypical controls (n=12, mean age: 5.8 years) were analyzed. Beta power in sleep, spindle density and percentage of slow wave sleep (SWS) were computed and compared between groups.
Results: Compared to typically developing, age-matched controls, children with Dup15q syndrome showed significantly elevated beta power in sleep (fro