Please use this identifier to cite or link to this item: https://ahro.austin.org.au/austinjspui/handle/1/16871
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dc.contributor.authorNguyen, Chinh D-
dc.contributor.authorWellman, Andrew-
dc.contributor.authorJordan, Amy S-
dc.contributor.authorEckert, Danny J-
dc.date.accessioned2017-09-26T23:12:23Z-
dc.date.available2017-09-26T23:12:23Z-
dc.date.issued2016-03-01-
dc.identifier.citationSleep 2016; 39(3): 541-550en_US
dc.identifier.urihttps://ahro.austin.org.au/austinjspui/handle/1/16871-
dc.description.abstractSTUDY OBJECTIVES: To determine the effects of mild airflow limitation on K-complex frequency and morphology and electroencephalogram (EEG) spectral power. METHODS: Transient reductions in continuous positive airway pressure (CPAP) during stable N2 sleep were performed to induce mild airflow limitation in 20 patients with obstructive sleep apnea (OSA) and 10 healthy controls aged 44 ± 13 y. EEG at C3 and airflow were measured in 1-min windows to quantify K-complex properties and EEG spectral power immediately before and during transient reductions in CPAP. The frequency and morphology (amplitude and latency of P200, N550 and N900 components) of K-complexes and EEG spectral power were compared between conditions. RESULTS: During mild airflow limitation (18% reduction in peak inspiratory airflow from baseline, 0.38 ± 0.11 versus 0.31 ± 0.1 L/sec) insufficient to cause American Academy of Sleep Medicine-defined cortical arousal, K-complex frequency (9.5 ± 4.5 versus 13.7 ± 6.4 per min, P < 0.01), N550 amplitude (25 ± 3 versus 27 ± 3 μV, P < 0.01) and EEG spectral power (delta: 147 ± 48 versus 230 ± 99 μV(2), P < 0.01 and theta bands: 31 ± 14 versus 34 ± 13 μV(2), P < 0.01) significantly increased whereas beta band power decreased (14 ± 5 versus 11 ± 4 μV(2), P < 0.01) compared to the preceding non flow-limited period on CPAP. K-complex frequency, morphology, and timing did not differ between patients and controls. CONCLUSION: Mild airflow limitation increases K-complex frequency, N550 amplitude, and spectral power of delta and theta bands. In addition to providing mechanistic insight into the role of mild airflow limitation on K-complex characteristics and EEG activity, these findings may have important implications for respiratory conditions in which airflow limitation during sleep is common (e.g., snoring and OSA).en_US
dc.subjectArousalen_US
dc.subjectObstructive sleep apneaen_US
dc.subjectSleep disordered breathingen_US
dc.subjectSnoringen_US
dc.titleMild airflow limitation during N2 sleep increases K-complex frequency and slows electroencephalographic activityen_US
dc.typeJournal Articleen_US
dc.identifier.journaltitleSleepen_US
dc.identifier.affiliationInstitute for Breathing and Sleep, Austin Health, Heidelberg, Victoria, Australiaen_US
dc.identifier.affiliationNeuroscience Research Australia (NeuRA), Randwick, New South Wales, Australiaen_US
dc.identifier.affiliationWoolcock Institute of Medical Research and Sydney Medical School, University of Sydney, Glebe, New South Wales, Australiaen_US
dc.identifier.affiliationBrigham and Women's Hospital and Harvard Medical School, Boston, MAen_US
dc.identifier.affiliationThe University of Melbourne, Parkville, Victoria, Australiaen_US
dc.identifier.affiliationSchool of Medical Sciences, University of New South Wales, Sydney, New South Wales, Australiaen_US
dc.identifier.doi10.5665/sleep.5522en_US
dc.type.contentTexten_US
dc.identifier.pubmedid26612389-
dc.type.austinJournal Articleen_US
local.name.researcherJordan, Amy S
item.openairetypeJournal Article-
item.cerifentitytypePublications-
item.grantfulltextnone-
item.fulltextNo Fulltext-
item.openairecristypehttp://purl.org/coar/resource_type/c_18cf-
crisitem.author.deptRespiratory and Sleep Medicine-
crisitem.author.deptInstitute for Breathing and Sleep-
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