Publication Date
7-1-2021
Journal
Anesthesia & Analgesia
DOI
10.1213/ANE.0000000000005273
PMID
33234943
PMCID
PMC8134503
PubMedCentral® Posted Date
7-1-2022
PubMedCentral® Full Text Version
Author MSS
Published Open-Access
yes
Keywords
Animals, Child, Hippocampus, Humans, Hypoxia, Learning, Sleep Apnea, Obstructive, Hippocampus, Intermittent Hypoxia, Learning and Memory, Neurocognition, Pediatric Obstructive Sleep Apnea, Reactive Oxygen Species
Abstract
This review provides an update on the neurocognitive phenotype of pediatric obstructive sleep apnea (OSA). Pediatric OSA is associated with neurocognitive deficits involving memory, learning, and executive functioning. Adenotonsillectomy (AT) is presently accepted as the first-line surgical treatment for pediatric OSA, but the executive function deficits do not resolve postsurgery, and the timeline for recovery remains unknown. This finding suggests that pediatric OSA potentially causes irreversible damage to multiple areas of the brain. The focus of this review is the hippocampus, 1 of the 2 major sites of postnatal neurogenesis, where new neurons are formed and integrated into existing circuitry and the mammalian center of learning/memory functions. Here, we review the clinical phenotype of pediatric OSA, and then discuss existing studies of OSA on different cell types in the hippocampus during critical periods of development. This will set the stage for future study using preclinical models to understand the pathogenesis of persistent neurocognitive dysfunction in pediatric OSA.
Included in
Anesthesiology Commons, Cognition and Perception Commons, Cognitive Behavioral Therapy Commons, Cognitive Psychology Commons, Neurology Commons, Neurosciences Commons