Sleep Architecture and Microstructure in Childhood Absence Epilepsy: Clinical and Neurophysiological Perspectives

Childhood absence epilepsy (CAE) is one of the most common epilepsy syndromes in childhood and has traditionally been regarded as a condition with a favorable neurological prognosis. However, increasing evidence suggests that CAE is associated with functional disturbances in neuronal networks that extend beyond seizure generation and may involve sleep and wakefulness regulation.

This narrative mini-review summarizes and critically discusses current clinical and neurophysiological evidence regarding alterations in sleep architecture and sleep electroencephalographic (EEG) microstructures in children with CAE, based on a focused analysis of selected clinical and observational studies.

The available data suggest that children with CAE, particularly before treatment initiation, may exhibit sleep macrostructure abnormalities, including reduced total sleep time, prolonged rapid eye movement sleep latency, increased arousal frequency, and decreased sleep efficiency. In addition, changes in sleep microstructure have been reported, most notably reduced sleep spindle density during stage-N2 sleep, especially in patients with concomitant cognitive impairment. These findings may reflect alterations in thalamocortical network function, although current evidence remains limited and heterogeneous.

Sleep disturbances appear to represent an important component of the clinical phenotype of childhood absence epilepsy. Assessing the sleep architecture and sleep EEG microstructure, particularly sleep spindles, may provide insights into network dysfunction and cognitive vulnerability; however, further studies are needed to clarify their clinical utility.