Clinical

Sleep EEG abnormalities in toddlers with regressive or classical autism

Dinstein will identify early neural abnormalities in two- to four-year-old toddlers with autism using whole-night EEG recordings in a hospital sleep lab. Furthermore, he will examine whether toddlers with regressive and classical autism exhibit distinct abnormalities that may indicate differences in their underlying pathology when comparing their brain activity and sleep architecture with that of typically developing toddlers.

A biomarker of reduced GABAergic action for assessing neural alterations in autism

Autism is a neurodevelopmental disorder in which individuals display a range of challenges in social cognition, language and sensory perception. Sensory perception issues include alterations in visual processing, including reductions in perceptual suppression evident in neuroimaging findings. Such changes in perceptual suppression have recently been shown to relate to reduced action of the inhibitory neurotransmitter GABA in individuals with autism[ref]Robertson C.E. et al. Curr. Biol. 26, 80–85 (2015) PubMed[/ref]. This finding, and others in the literature, support the idea that alterations in GABAergic signaling, which cause an imbalance in excitatory/inhibitory neurotransmission, reflect a central characteristic of the neurobiology of autism. This suggests that the GABAergic pathway represents a viable target for drug therapy in autism. Successful development of such drug therapies will require the identification and validation of suitable biomarkers to track neural alterations in GABAergic signaling.

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