High-density electroencephalographic recordings during sleep in children with disorders of consciousness.

Neuroimage Clin

Child Development Centre and Paediatric Sleep Disorders Centre, University Children's Hospital Zurich, Switzerland; Children's Research Centre, University Children's Hospital Zurich, Switzerland; University Clinics for Child and Adolescent Psychiatry, University of Zurich, Switzerland. Electronic address:

Published: December 2016

AI Article Synopsis

  • A study investigates brain function in children with disorders of consciousness (DOC) using EEG recordings during sleep, focusing on sleep slow waves (SWA).
  • Children with DOC exhibited lower SWA build-up compared to healthy peers and those with injuries but without DOC, particularly in the parietal brain area.
  • The findings indicate that reduced SWA regulation could serve as a marker for brain dysfunction in children with DOC, suggesting its potential for future assessments in both adults and children.

Article Abstract

Introduction: A large number of studies have investigated neural correlates of consciousness in adults. However, knowledge about brain function in children with disorders of consciousness (DOC) is very limited. We suggest that EEG recordings during sleep are a promising approach. In healthy adults as well as in children, it has been shown that the activity of sleep slow waves (EEG spectral power 1-4.5 Hz), the primary characteristic of deep sleep, is dependent on use during previous wakefulness. Thus the regulation of slow wave activity (SWA) provides indirect insights into brain function during wakefulness.

Methods: In the present study, we investigated high-density EEG recordings during sleep in ten healthy children and in ten children with acquired brain injury, including five children with DOC and five children with acquired brain injury without DOC. We used the build-up of SWA to quantify SWA regulation.

Results: Children with DOC showed a global reduction in the SWA build-up when compared to both, healthy children and children with acquired brain injury without DOC. This reduction was most pronounced over parietal brain areas. Comparisons within the group of children with DOC revealed that the parietal SWA build-up was the lowest in patients showing poor outcome. Longitudinal measurements during the recovery period showed an increase in parietal SWA build-up from the first to the second sleep recording.

Conclusions: Our results suggest that the reduced parietal SWA regulation may represent a characteristic topographical marker for brain network dysfunction in children with DOC. In the future, the regulation of SWA might be used as a complementary assessment in adult and paediatric patients with DOC.

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Source
http://www.ncbi.nlm.nih.gov/pmc/articles/PMC4827803PMC
http://dx.doi.org/10.1016/j.nicl.2016.03.012DOI Listing

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