| Literature DB >> 33234943 |
Arvind Chandrakantan1,2, Adam C Adler1,2, Mehmet Tohsun3, Farrah Kheradamand4,5,6,7,8, Russell S Ray9,10,11, Steven Roth12,13.
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.Entities:
Mesh:
Year: 2021 PMID: 33234943 PMCID: PMC8134503 DOI: 10.1213/ANE.0000000000005273
Source DB: PubMed Journal: Anesth Analg ISSN: 0003-2999 Impact factor: 6.627