0142 The Cumulative Effect of Partial Chronic Sleep Restriction on the Neural Processing Stream in Neurologically Normal Individuals

Introduction Event-related potentials (ERP) are averaged electroencephalogram (EEG) responses to stimuli enabling precise temporal characterization of neural processing. We analyzed the temporal evolution and course of cognitive processing impairments during a 16 day randomized, cross-over sleep res...

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Veröffentlicht in:Sleep (New York, N.Y.) N.Y.), 2019-04, Vol.42 (Supplement_1), p.A58-A59
Hauptverfasser: Gossard, Thomas R, Westerland, Sarah M, Linn-Evans, Maria, Timm, Paul C, Sandness, David J, Dueffert, Lucas, Feemster, John C, McCarter, Stuart J, Teigen, Luke, Covassin, Naima, Svatikova, Anna, Ruzek, Lucas, Bukartyk, Jan, Somers, Virend K, St. Louis, Erik K
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container_issue Supplement_1
container_start_page A58
container_title Sleep (New York, N.Y.)
container_volume 42
creator Gossard, Thomas R
Westerland, Sarah M
Linn-Evans, Maria
Timm, Paul C
Sandness, David J
Dueffert, Lucas
Feemster, John C
McCarter, Stuart J
Teigen, Luke
Covassin, Naima
Svatikova, Anna
Ruzek, Lucas
Bukartyk, Jan
Somers, Virend K
St. Louis, Erik K
description Introduction Event-related potentials (ERP) are averaged electroencephalogram (EEG) responses to stimuli enabling precise temporal characterization of neural processing. We analyzed the temporal evolution and course of cognitive processing impairments during a 16 day randomized, cross-over sleep restriction experiment, by analyzing visual attention (N2pc), stimulus classification (P3), and decision making (error-related negativity (ERN) and positivity (Pe)) ERPs. Methods Eighteen healthy subjects (8 women, 10 men; age 22.8±4.88, range 18-36 years underwent sleep restriction (3 acclimation nights of 9 hours of time in bed, then 9 experimental 4 hours nights, then 3 recovery sleep nights), and control sleep (15 nights at 9 hours of time in bed) sequences in random order. EEG recordings during a visual attention task were completed once (day 3) during the acclimation period, 3 times during the experimental period (days 5, 6, 9), and once in the recovery period (day 15). Post-hoc off-line ERP data processing yielded N2pc, P3, and ERN/Pe waveforms with comparison of primary amplitude and latency measures across experimental timepoints utilizing mixed linear regression modeling. Results ERN and Pe amplitudes were significantly reduced during sleep restricted days 6 and 9 (both p
doi_str_mv 10.1093/sleep/zsz067.141
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We analyzed the temporal evolution and course of cognitive processing impairments during a 16 day randomized, cross-over sleep restriction experiment, by analyzing visual attention (N2pc), stimulus classification (P3), and decision making (error-related negativity (ERN) and positivity (Pe)) ERPs. Methods Eighteen healthy subjects (8 women, 10 men; age 22.8±4.88, range 18-36 years underwent sleep restriction (3 acclimation nights of 9 hours of time in bed, then 9 experimental 4 hours nights, then 3 recovery sleep nights), and control sleep (15 nights at 9 hours of time in bed) sequences in random order. EEG recordings during a visual attention task were completed once (day 3) during the acclimation period, 3 times during the experimental period (days 5, 6, 9), and once in the recovery period (day 15). Post-hoc off-line ERP data processing yielded N2pc, P3, and ERN/Pe waveforms with comparison of primary amplitude and latency measures across experimental timepoints utilizing mixed linear regression modeling. Results ERN and Pe amplitudes were significantly reduced during sleep restricted days 6 and 9 (both p&lt;0.05, for Pe p&lt;0.02), and P3 amplitude was significantly lower during sleep restricted days 9 and 15 (both p&lt;0.02), compared to corresponding control sequence days. Pe (day 6) and P3 (days 5,6,9) fractional area latencies were also significantly delayed during sleep restriction compared to the corresponding control sequence days (both p&lt;0.03). There were no significant N2pc amplitude or latency differences between conditions. Conclusion These data suggest that stimulus classification and error-monitoring, reflecting mesial temporal and frontal neuronal network processing, are selectively impaired during chronic sleep restriction. Covert attentional shifting remained intact, implying greater allocation of top-down executive resources toward preserving attentional capacity at the cost of degraded error monitoring capacities during sleep restriction. Further research analyzing sleep homeostatic drive and vigilance is planned to determine whether these brain functions influence visual processing efficiency. Support (If Any) NIH/NHLBI R01 HL 114676; Mayo Clinic CCaTS 1 UL1 RR024150-01</description><identifier>ISSN: 0161-8105</identifier><identifier>EISSN: 1550-9109</identifier><identifier>DOI: 10.1093/sleep/zsz067.141</identifier><language>eng</language><publisher>Westchester: Oxford University Press</publisher><subject>Sleep</subject><ispartof>Sleep (New York, N.Y.), 2019-04, Vol.42 (Supplement_1), p.A58-A59</ispartof><rights>Sleep Research Society 2019. Published by Oxford University Press on behalf of the Sleep Research Society. All rights reserved. For permissions, please e-mail journals.permissions@oup.com.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c1581-d2fea6df8d59e0542bbb24b852b81ffd54fb0c0c9881650f24a025eb880a4aad3</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids></links><search><creatorcontrib>Gossard, Thomas R</creatorcontrib><creatorcontrib>Westerland, Sarah M</creatorcontrib><creatorcontrib>Linn-Evans, Maria</creatorcontrib><creatorcontrib>Timm, Paul C</creatorcontrib><creatorcontrib>Sandness, David J</creatorcontrib><creatorcontrib>Dueffert, Lucas</creatorcontrib><creatorcontrib>Feemster, John C</creatorcontrib><creatorcontrib>McCarter, Stuart J</creatorcontrib><creatorcontrib>Teigen, Luke</creatorcontrib><creatorcontrib>Covassin, Naima</creatorcontrib><creatorcontrib>Svatikova, Anna</creatorcontrib><creatorcontrib>Ruzek, Lucas</creatorcontrib><creatorcontrib>Bukartyk, Jan</creatorcontrib><creatorcontrib>Somers, Virend K</creatorcontrib><creatorcontrib>St. Louis, Erik K</creatorcontrib><title>0142 The Cumulative Effect of Partial Chronic Sleep Restriction on the Neural Processing Stream in Neurologically Normal Individuals</title><title>Sleep (New York, N.Y.)</title><description>Introduction Event-related potentials (ERP) are averaged electroencephalogram (EEG) responses to stimuli enabling precise temporal characterization of neural processing. We analyzed the temporal evolution and course of cognitive processing impairments during a 16 day randomized, cross-over sleep restriction experiment, by analyzing visual attention (N2pc), stimulus classification (P3), and decision making (error-related negativity (ERN) and positivity (Pe)) ERPs. Methods Eighteen healthy subjects (8 women, 10 men; age 22.8±4.88, range 18-36 years underwent sleep restriction (3 acclimation nights of 9 hours of time in bed, then 9 experimental 4 hours nights, then 3 recovery sleep nights), and control sleep (15 nights at 9 hours of time in bed) sequences in random order. EEG recordings during a visual attention task were completed once (day 3) during the acclimation period, 3 times during the experimental period (days 5, 6, 9), and once in the recovery period (day 15). Post-hoc off-line ERP data processing yielded N2pc, P3, and ERN/Pe waveforms with comparison of primary amplitude and latency measures across experimental timepoints utilizing mixed linear regression modeling. Results ERN and Pe amplitudes were significantly reduced during sleep restricted days 6 and 9 (both p&lt;0.05, for Pe p&lt;0.02), and P3 amplitude was significantly lower during sleep restricted days 9 and 15 (both p&lt;0.02), compared to corresponding control sequence days. Pe (day 6) and P3 (days 5,6,9) fractional area latencies were also significantly delayed during sleep restriction compared to the corresponding control sequence days (both p&lt;0.03). There were no significant N2pc amplitude or latency differences between conditions. Conclusion These data suggest that stimulus classification and error-monitoring, reflecting mesial temporal and frontal neuronal network processing, are selectively impaired during chronic sleep restriction. Covert attentional shifting remained intact, implying greater allocation of top-down executive resources toward preserving attentional capacity at the cost of degraded error monitoring capacities during sleep restriction. Further research analyzing sleep homeostatic drive and vigilance is planned to determine whether these brain functions influence visual processing efficiency. 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We analyzed the temporal evolution and course of cognitive processing impairments during a 16 day randomized, cross-over sleep restriction experiment, by analyzing visual attention (N2pc), stimulus classification (P3), and decision making (error-related negativity (ERN) and positivity (Pe)) ERPs. Methods Eighteen healthy subjects (8 women, 10 men; age 22.8±4.88, range 18-36 years underwent sleep restriction (3 acclimation nights of 9 hours of time in bed, then 9 experimental 4 hours nights, then 3 recovery sleep nights), and control sleep (15 nights at 9 hours of time in bed) sequences in random order. EEG recordings during a visual attention task were completed once (day 3) during the acclimation period, 3 times during the experimental period (days 5, 6, 9), and once in the recovery period (day 15). Post-hoc off-line ERP data processing yielded N2pc, P3, and ERN/Pe waveforms with comparison of primary amplitude and latency measures across experimental timepoints utilizing mixed linear regression modeling. Results ERN and Pe amplitudes were significantly reduced during sleep restricted days 6 and 9 (both p&lt;0.05, for Pe p&lt;0.02), and P3 amplitude was significantly lower during sleep restricted days 9 and 15 (both p&lt;0.02), compared to corresponding control sequence days. Pe (day 6) and P3 (days 5,6,9) fractional area latencies were also significantly delayed during sleep restriction compared to the corresponding control sequence days (both p&lt;0.03). There were no significant N2pc amplitude or latency differences between conditions. Conclusion These data suggest that stimulus classification and error-monitoring, reflecting mesial temporal and frontal neuronal network processing, are selectively impaired during chronic sleep restriction. Covert attentional shifting remained intact, implying greater allocation of top-down executive resources toward preserving attentional capacity at the cost of degraded error monitoring capacities during sleep restriction. Further research analyzing sleep homeostatic drive and vigilance is planned to determine whether these brain functions influence visual processing efficiency. Support (If Any) NIH/NHLBI R01 HL 114676; Mayo Clinic CCaTS 1 UL1 RR024150-01</abstract><cop>Westchester</cop><pub>Oxford University Press</pub><doi>10.1093/sleep/zsz067.141</doi><oa>free_for_read</oa></addata></record>
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title 0142 The Cumulative Effect of Partial Chronic Sleep Restriction on the Neural Processing Stream in Neurologically Normal Individuals
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