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Abstract
The development of neural circuits has long-lasting effects on brain function, yet our understanding of early circuit development in humans remains limited. Here, periodic EEG power features and aperiodic components were examined from longitudinal EEGs collected from 592 healthy 2–44 month-old infants, revealing age-dependent nonlinear changes suggestive of distinct milestones in early brain maturation. Developmental changes in periodic peaks include (1) the presence and then absence of a 9-10 Hz alpha peak between 2-6 months, (2) nonlinear changes in high beta peaks (20-30 Hz) between 4-18 months, and (3) the emergence of a low beta peak (12-20 Hz) in some infants after six months of age. We hypothesized that the emergence of the low beta peak may reflect maturation of thalamocortical network development. Infant anesthesia studies observe that GABA-modulating anesthetics do not induce thalamocortical mediated frontal alpha coherence until 10-12 months of age. Using a small cohort of infants (n = 23) with EEG before and during GABA-modulating anesthesia, we provide preliminary evidence that infants with a low beta peak have higher anesthesia-induced alpha coherence compared to those without a low beta peak.
Using longitudinal EEG data from 592 infants and toddlers, the authors identify age-dependent nonlinear changes in periodic alpha and beta peaks suggestive of distinct milestones in early brain maturation, including thalamocortical network development.
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1 Boston Children’s Hospital, Division of Developmental Medicine, Boston, USA (GRID:grid.2515.3) (ISNI:0000 0004 0378 8438); Harvard Medical School, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X)
2 Albert Einstein College of Medicine, Department of Anesthesiology, Montefiore Medical Center, Children’s Hospital at Montefiore, Bronx, USA (GRID:grid.251993.5) (ISNI:0000000121791997)
3 Hospital Clínico de la Universidad de Chile, Departamento de Anestesia y Medicina Perioperatoria, Santiago, Chile (GRID:grid.412248.9); Massachusetts General Hospital, Department of Anesthesia, Critical Care and Pain Medicine, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924)
4 Harvard Medical School, Department of Neurobiology, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Harvard University, Program in Neuroscience, Division of Medical Sciences, Graduate School of Arts and Sciences, Cambridge, USA (GRID:grid.38142.3c) (ISNI:0000 0004 1936 754X)
5 Albert Einstein College of Medicine, The Saul R. Korey Department of Neurology, Montefiore Medical Center, Bronx, USA (GRID:grid.251993.5) (ISNI:0000000121791997); Albert Einstein College of Medicine, Department of Epidemiology and Population Health, Bronx, USA (GRID:grid.251993.5) (ISNI:0000 0001 2179 1997)
6 Massachusetts General Hospital, Department of Anesthesia, Critical Care and Pain Medicine, Boston, USA (GRID:grid.32224.35) (ISNI:0000 0004 0386 9924)
7 Boston Children’s Hospital, Division of Developmental Medicine, Boston, USA (GRID:grid.2515.3) (ISNI:0000 0004 0378 8438); Harvard Medical School, Boston, USA (GRID:grid.38142.3c) (ISNI:000000041936754X); Harvard Graduate School of Education, Cambridge, USA (GRID:grid.38142.3c) (ISNI:000000041936754X)