Regional brain tissue integrity in pediatric obstructive sleep apnea

•We assess nature and extent of tissue changes in pediatric OSA.•Pediatric OSA show acute injury in cognitive, mood, and autonomic sites.•OSA subjects have structural basis for cognitive and behavioural deficits. Children with long-standing obstructive sleep apnea (OSA) show evidence of neural injur...

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Veröffentlicht in:Neuroscience letters 2018-08, Vol.682, p.118-123
Hauptverfasser: Kheirandish-Gozal, Leila, Sahib, Ashish K., Macey, Paul M., Philby, Mona F., Gozal, David, Kumar, Rajesh
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Sprache:eng
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Zusammenfassung:•We assess nature and extent of tissue changes in pediatric OSA.•Pediatric OSA show acute injury in cognitive, mood, and autonomic sites.•OSA subjects have structural basis for cognitive and behavioural deficits. Children with long-standing obstructive sleep apnea (OSA) show evidence of neural injury and functional deficits in behavioral and cognitive regulatory brain regions that are reflected in symptoms of altered cognitive performance and behaviors. While we earlier showed reduced gray matter volume and increased and reduced regional cortical thicknesses, such structural changes give little indication of the underlying pathology. Brain tissue integrity in pediatric OSA subjects can reflect the nature and extent of injury or structural adaptation, and can be assessed by entropy tissue texture, a measure of local changes in signal intensity patterns from high-resolution magnetic resonance images. We collected high-resolution T1-weighted magnetic resonance images from 10 pediatric OSA (age, 7.9 ± 1.1 years; apnea-hypopnea-index, 8.8 ± 3.0 events/hour; body-mass-index, 20 ± 6.7 kg/m2; 7 male) and 8 healthy controls (age, 8.8 ± 1.6 years; body-mass-index, 19.6 ± 5.9 kg/m2; 5 female). Images were bias-corrected and entropy maps calculated, individual maps were normalized to a common space, smoothed, and compared between groups (ANCOVA; covariates: age, gender; SPM12, uncorrected-threshold p 
ISSN:0304-3940
1872-7972
DOI:10.1016/j.neulet.2018.06.002