Dual-tasking alleviated sleep deprivation disruption in visuomotor tracking: An fMRI study
Identifieur interne : 002487 ( Main/Merge ); précédent : 002486; suivant : 002488Dual-tasking alleviated sleep deprivation disruption in visuomotor tracking: An fMRI study
Auteurs : Yunglin Gazes [États-Unis] ; Brian C. Rakitin [États-Unis] ; Jason Steffener [États-Unis] ; Christian Habeck [États-Unis] ; Brady Butterfield [États-Unis] ; Robert C. Basner [États-Unis] ; Claude Ghez [États-Unis] ; Yaakov Stern [États-Unis]Source :
- Brain and Cognition [ 0278-2626 ] ; 2012.
Abstract
Effects of dual-responding on tracking performance after 49-hr of sleep deprivation (SD) were evaluated behaviorally and with functional magnetic resonance imaging (fMRI). Continuous visuomotor tracking was performed simultaneously with an intermittent color-matching visual detection task in which a pair of color-matched stimuli constituted a target and non-matches were non-targets. Tracking error means were binned time-locked to stimulus onset of the detection task in order to observe changes associated with dual-responding by comparing the error during targets and non-targets. Similar comparison was made with fMRI data. Our result showed that despite a significant increase in the overall tracking error post SD, from 20 pixels pre SD to 45 pixels post SD, error decreased to a minimum of about 25 pixels 0 to 6 s after dual-response. Despite an overall reduced activation post SD, greater activation difference between targets and non-targets was found post SD in task-related regions, such as the left cerebellum, the left somatosensory cortex, the left extrastriate cortex, bilateral precuneus, the left middle frontal gyrus, and the left motor cortex. Our results suggest that dual-response helps to alleviate performance impairment usually associated with SD. The duration of the alleviation effect was on the order of seconds after dual-responding.
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DOI: 10.1016/j.bandc.2012.01.004
PubMed: 22305924
PubMed Central: 3278524
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Basner</name><affiliation wicri:level="2"><nlm:aff id="A2">Medicine - Pulmonary, Allergy & Critical Care, Columbia University, 630 West 168<sup>th</sup> Street, PH 8 Center, Room 859, New York, New York 10032</nlm:aff><country xml:lang="fr">États-Unis</country><placeName><region type="state">État de New York</region></placeName><wicri:cityArea> Street, PH 8 Center, Room 859, New York</wicri:cityArea></affiliation></author><author><name sortKey="Ghez, Claude" sort="Ghez, Claude" uniqKey="Ghez C" first="Claude" last="Ghez">Claude Ghez</name><affiliation wicri:level="4"><nlm:aff id="A3">Department of Neurology and Neuroscience, Columbia University, 821 Psychiatric Institute Annex, 1051 Riverside Drive, New York, NY 10032, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Department of Neurology and Neuroscience, Columbia University, 821 Psychiatric Institute Annex, 1051 Riverside Drive, New York, NY 10032</wicri:regionArea><placeName><region type="state">État de New York</region></placeName><orgName type="university">Université Columbia</orgName></affiliation></author><author><name sortKey="Stern, Yaakov" sort="Stern, Yaakov" uniqKey="Stern Y" first="Yaakov" last="Stern">Yaakov Stern</name><affiliation wicri:level="4"><nlm:aff id="A1">Cognitive Neuroscience Division, Taub Institute, Columbia University, 630 West 168th Street, P & S Box 16, New York, NY 10032, USA</nlm:aff><country xml:lang="fr">États-Unis</country><wicri:regionArea>Cognitive Neuroscience Division, Taub Institute, Columbia University, 630 West 168th Street, P & S Box 16, New York, NY 10032</wicri:regionArea><placeName><region type="state">État de New York</region></placeName><orgName type="university">Université Columbia</orgName></affiliation></author></analytic><series><title level="j">Brain and Cognition</title><idno type="ISSN">0278-2626</idno><idno type="eISSN">1090-2147</idno><imprint><date when="2012">2012</date></imprint></series></biblStruct></sourceDesc></fileDesc><profileDesc><textClass></textClass></profileDesc></teiHeader><front><div type="abstract" xml:lang="en"><p id="P1">Effects of dual-responding on tracking performance after 49-hr of sleep deprivation (SD) were evaluated behaviorally and with functional magnetic resonance imaging (fMRI). Continuous visuomotor tracking was performed simultaneously with an intermittent color-matching visual detection task in which a pair of color-matched stimuli constituted a target and non-matches were non-targets. Tracking error means were binned time-locked to stimulus onset of the detection task in order to observe changes associated with dual-responding by comparing the error during targets and non-targets. Similar comparison was made with fMRI data. Our result showed that despite a significant increase in the overall tracking error post SD, from 20 pixels pre SD to 45 pixels post SD, error decreased to a minimum of about 25 pixels 0 to 6 s after dual-response. Despite an overall reduced activation post SD, greater activation difference between targets and non-targets was found post SD in task-related regions, such as the left cerebellum, the left somatosensory cortex, the left extrastriate cortex, bilateral precuneus, the left middle frontal gyrus, and the left motor cortex. Our results suggest that dual-response helps to alleviate performance impairment usually associated with SD. The duration of the alleviation effect was on the order of seconds after dual-responding.</p></div></front></TEI></record>Pour manipuler ce document sous Unix (Dilib)
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