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      Classifying attentional vulnerability to total sleep deprivation using baseline features of Psychomotor Vigilance Test performance

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          Abstract

          There are strong individual differences in performance during sleep deprivation. We assessed whether baseline features of Psychomotor Vigilance Test (PVT) performance can be used for classifying participants’ relative attentional vulnerability to total sleep deprivation. In a laboratory, healthy adults (n = 160, aged 18–30 years) completed a 10-min PVT every 2 h while being kept awake for ≥24 hours. Participants were categorized as vulnerable (n = 40), intermediate (n = 80), or resilient (n = 40) based on their number of PVT lapses during one night of sleep deprivation. For each baseline PVT (taken 4–14 h after wake-up time), a linear discriminant model with wrapper-based feature selection was used to classify participants’ vulnerability to subsequent sleep deprivation. Across models, classification accuracy was about 70% (range 65–76%) using stratified 5-fold cross validation. The models provided about 78% sensitivity and 86% specificity for classifying resilient participants, and about 70% sensitivity and 89% specificity for classifying vulnerable participants. These results suggest features derived from a single 10-min PVT at baseline can provide substantial, but incomplete information about a person’s relative attentional vulnerability to total sleep deprivation. In the long term, modeling approaches that incorporate baseline performance characteristics can potentially improve personalized predictions of attentional performance when sleep deprivation cannot be avoided.

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          Wrappers for feature subset selection

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            Developing criteria for establishing interrater reliability of specific items: applications to assessment of adaptive behavior.

            A set of criteria based upon biostatistical considerations for determining the interrater reliability of specific adaptive behavior items in a given setting was presented. The advantages and limitations of extant statistical assessment procedures were discussed. Also, a set of guidelines for differentiating type of adaptive behavior that are statistically reliable from those that are reliable in a clinical or practical sense was delineated. Data sets were presented throughout in order to illustrate the advantages of recommended statistical procedures over other available ones.
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              Cumulative sleepiness, mood disturbance, and psychomotor vigilance performance decrements during a week of sleep restricted to 4-5 hours per night.

              To determine whether a cumulative sleep debt (in a range commonly experienced) would result in cumulative changes in measures of waking neurobehavioral alertness, 16 healthy young adults had their sleep restricted 33% below habitual sleep duration, to an average 4.98 hours per night [standard deviation (SD) = 0.57] for seven consecutive nights. Subjects slept in the laboratory, and sleep and waking were monitored by staff and actigraphy. Three times each day (1000, 1600, and 2200 hours) subjects were assessed for subjective sleepiness (SSS) and mood (POMS) and were evaluated on a brief performance battery that included psychomotor vigilance (PVT), probed memory (PRM), and serial-addition testing, Once each day they completed a series of visual analog scales (VAS) and reported sleepiness and somatic and cognitive/emotional problems. Sleep restriction resulted in statistically robust cumulative effects on waking functions. SSS ratings, subscale scores for fatigue, confusion, tension, and total mood disturbance from the POMS and VAS ratings of mental exhaustion and stress were evaluated across days of restricted sleep (p = 0.009 to p = 0.0001). PVT performance parameters, including the frequency and duration of lapses, were also significantly increased by restriction (p = 0.018 to p = 0.0001). Significant time-of-day effects were evident in SSS and PVT data, but time-of-day did not interact with the effects of sleep restriction across days. The temporal profiles of cumulative changes in neurobehavioral measures of alertness as a function of sleep restriction were generally consistent. Subjective changes tended to precede performance changes by 1 day, but overall changes in both classes of measure were greatest during the first 2 days (P1, P2) and last 2 days (P6, P7) of sleep restriction. Data from subsets of subjects also showed: 1) that significant decreases in the MSLT occurred during sleep restriction, 2) that the elevated sleepiness and performance deficits continued beyond day 7 of restriction, and 3) that recovery from these deficits appeared to require two full nights of sleep. The cumulative increase in performance lapses across days of sleep restriction correlated closely with MSLT results (r = -0.95) from an earlier comparable experiment by Carskadon and Dement (1). These findings suggest that cumulative nocturnal sleep debt had a dynamic and escalating analog in cumulative daytime sleepiness and that asymptotic or steady-state sleepiness was not achieved in response to sleep restriction.
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                Author and article information

                Contributors
                joshua.gooley@duke-nus.edu.sg
                Journal
                Sci Rep
                Sci Rep
                Scientific Reports
                Nature Publishing Group UK (London )
                2045-2322
                20 August 2019
                20 August 2019
                2019
                : 9
                : 12102
                Affiliations
                [1 ]ISNI 0000 0004 0385 0924, GRID grid.428397.3, Center for Cognitive Neuroscience, , Duke-NUS Medical School, ; Singapore, 169857 Singapore
                [2 ]ISNI 0000 0004 0385 0924, GRID grid.428397.3, Neuroscience and Behavioral Disorders Program, , Duke-NUS Medical School, ; Singapore, 169857 Singapore
                [3 ]ISNI 0000 0004 0378 8294, GRID grid.62560.37, Division of Sleep and Circadian Disorders, Departments of Medicine and Neurology, , Brigham and Women’s Hospital, ; Boston, MA 02115 USA
                [4 ]ISNI 000000041936754X, GRID grid.38142.3c, Division of Sleep Medicine, Harvard Medical School, ; Boston, MA 02115 USA
                Article
                48280
                10.1038/s41598-019-48280-4
                6702200
                31431644
                388e8662-46ab-48a4-8001-81f634ca990c
                © The Author(s) 2019

                Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this license, visit http://creativecommons.org/licenses/by/4.0/.

                History
                : 27 March 2019
                : 29 July 2019
                Funding
                Funded by: FundRef https://doi.org/10.13039/100008898, National Space Biomedical Research Institute (NSBRI);
                Award ID: NASA NCC 9-58
                Award ID: NASA NCC 9-58
                Award ID: NASA NCC 9-58
                Award ID: NASA NCC 9-58
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000002, U.S. Department of Health & Human Services | National Institutes of Health (NIH);
                Award ID: NIMH R01 MH45130
                Award ID: NCCAM R01 AT002129
                Award ID: NHLBI K24HL105664
                Award ID: M01 RR02635
                Award ID: T32-HL07901
                Award ID: NIMH R01 MH45130
                Award ID: NCCAM R01 AT002129
                Award ID: NHLBI K24HL105664
                Award ID: M01 RR02635
                Award ID: T32-HL07901
                Award ID: NIMH R01 MH45130
                Award ID: NCCAM R01 AT002129
                Award ID: NHLBI K24HL105664
                Award ID: M01 RR02635
                Award ID: T32-HL07901
                Award ID: NIMH R01 MH45130
                Award ID: NCCAM R01 AT002129
                Award ID: NHLBI K24HL105664
                Award ID: M01 RR02635
                Award ID: T32-HL07901
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000006, United States Department of Defense | United States Navy | Office of Naval Research (ONR);
                Award ID: N00014-15-1-2408
                Award ID: N00014-15-1-2408
                Award ID: N00014-15-1-2408
                Award Recipient :
                Funded by: FundRef https://doi.org/10.13039/100000185, United States Department of Defense | Defense Advanced Research Projects Agency (DARPA);
                Award ID: N66001-13-C-4035
                Award ID: N66001-13-C-4035
                Award ID: N66001-13-C-4035
                Award ID: N66001-13-C-4035
                Award ID: N66001-13-C-4035
                Award Recipient :
                Funded by: Duke-NUS Signature Research Program funded by the Agency for Science, Technology and Research, Singapore, and the Ministry of Health, Singapore
                Categories
                Article
                Custom metadata
                © The Author(s) 2019

                Uncategorized
                sleep deprivation,attention
                Uncategorized
                sleep deprivation, attention

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