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Article: Sleep and Inhibitory Control Over Mood-Congruent Information in Emerging Adults With Depressive Disorder

TitleSleep and Inhibitory Control Over Mood-Congruent Information in Emerging Adults With Depressive Disorder
Authors
Issue Date11-Dec-2021
PublisherLippincott, Williams & Wilkins
Citation
Psychosomatic Medicine: Journal of Biobehavioral Medicine, 2021, v. 83, n. 9, p. 1004-1012 How to Cite?
Abstract

Objective Accumulating evidence has suggested bidirectionality between sleep problems and depression, but the underlying mechanism is unclear. We assessed the role of sleep in inhibitory control ability with emotional stimuli, which has been shown to be suboptimal among individuals with depression and proposed to perpetuate depressive symptoms. Methods Emerging adults (aged 18-25 years, 64.6% female) were screened for depressive and other mental disorders by structured clinical interview and questionnaire. Individuals with depressive disorders were assigned to have a polysomnography-monitored daytime sleep opportunity (Sleep-Dep, n = 20), whereas nondepressed individuals were randomized to either have daytime sleep (Sleep-Ctrl, n = 27) or stay awake (Wake-Ctrl, n = 18). Participants completed the Affective Go/No-Go Task two times, separated by experimental conditions. Results A factorial model with a between-subject factor (Sleep-Dep/Sleep-Ctrl/Wake-Ctrl) and a within-subject factor (test 1/test 2) was used to assess if the groups differed in inhibitory control across test sessions, as inferred by changes in d-prime and false alarm rates (FA). Results from mixed factorial models showed a significant interaction effect between time and group on FA in the block with neutral faces as the target and happy faces as the nontarget (F(2,61) = 5.15, pfdr =.045). Although Sleep-Dep had decreased FA after sleep (t(19) = 2.94, pfdr =.050), Sleep-Ctrl and Wake-Ctrl had no significant between-session changes (p values >.05). Postsleep improvement in FA in Sleep-Dep correlated with longer stage 2 sleep (r(20) = 0.788, pfdr <.001) and stage 2 fast spindle number at O1 (r(18) = 0.692, pfdr =.015). Conclusions Sleep gain, particularly stage 2 sleep and related physiology, potentially enhances inhibitory control ability responding to emotional information among individuals with depressive disorders.


Persistent Identifierhttp://hdl.handle.net/10722/345853
ISSN
2023 Impact Factor: 2.9
2023 SCImago Journal Rankings: 1.081

 

DC FieldValueLanguage
dc.contributor.authorLau, Esther Yuet Ying-
dc.contributor.authorWong, Mark Lawrence-
dc.contributor.authorLam, Yeuk Ching-
dc.contributor.authorLau, Kristy Nga Ting-
dc.contributor.authorChung, Ka Fai-
dc.contributor.authorRusak, Benjamin-
dc.date.accessioned2024-09-04T07:05:56Z-
dc.date.available2024-09-04T07:05:56Z-
dc.date.issued2021-12-11-
dc.identifier.citationPsychosomatic Medicine: Journal of Biobehavioral Medicine, 2021, v. 83, n. 9, p. 1004-1012-
dc.identifier.issn0033-3174-
dc.identifier.urihttp://hdl.handle.net/10722/345853-
dc.description.abstract<p>Objective Accumulating evidence has suggested bidirectionality between sleep problems and depression, but the underlying mechanism is unclear. We assessed the role of sleep in inhibitory control ability with emotional stimuli, which has been shown to be suboptimal among individuals with depression and proposed to perpetuate depressive symptoms. Methods Emerging adults (aged 18-25 years, 64.6% female) were screened for depressive and other mental disorders by structured clinical interview and questionnaire. Individuals with depressive disorders were assigned to have a polysomnography-monitored daytime sleep opportunity (Sleep-Dep, n = 20), whereas nondepressed individuals were randomized to either have daytime sleep (Sleep-Ctrl, n = 27) or stay awake (Wake-Ctrl, n = 18). Participants completed the Affective Go/No-Go Task two times, separated by experimental conditions. Results A factorial model with a between-subject factor (Sleep-Dep/Sleep-Ctrl/Wake-Ctrl) and a within-subject factor (test 1/test 2) was used to assess if the groups differed in inhibitory control across test sessions, as inferred by changes in d-prime and false alarm rates (FA). Results from mixed factorial models showed a significant interaction effect between time and group on FA in the block with neutral faces as the target and happy faces as the nontarget (F(2,61) = 5.15, pfdr =.045). Although Sleep-Dep had decreased FA after sleep (t(19) = 2.94, pfdr =.050), Sleep-Ctrl and Wake-Ctrl had no significant between-session changes (p values >.05). Postsleep improvement in FA in Sleep-Dep correlated with longer stage 2 sleep (r(20) = 0.788, pfdr <.001) and stage 2 fast spindle number at O1 (r(18) = 0.692, pfdr =.015). Conclusions Sleep gain, particularly stage 2 sleep and related physiology, potentially enhances inhibitory control ability responding to emotional information among individuals with depressive disorders.</p>-
dc.languageeng-
dc.publisherLippincott, Williams & Wilkins-
dc.relation.ispartofPsychosomatic Medicine: Journal of Biobehavioral Medicine-
dc.rightsThis work is licensed under a Creative Commons Attribution-NonCommercial-NoDerivatives 4.0 International License.-
dc.titleSleep and Inhibitory Control Over Mood-Congruent Information in Emerging Adults With Depressive Disorder-
dc.typeArticle-
dc.description.naturepublished_or_final_version-
dc.identifier.doi10.1097/PSY.0000000000000996-
dc.identifier.pmid34419999-
dc.identifier.scopuseid_2-s2.0-85121952887-
dc.identifier.volume83-
dc.identifier.issue9-
dc.identifier.spage1004-
dc.identifier.epage1012-
dc.identifier.eissn1534-7796-
dc.identifier.issnl0033-3174-

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