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Abnormal functional connectivity density in sleep-deprived subjects
Sleep deprivation (SD) can alter the intrinsic brain functional organization. However, its effects on intrinsic low-frequency connectivity in the whole brain have not been well characterized. In this study, we used voxel-based functional connectivity density (FCD) analysis to investigate the effects...
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Published in: | Brain imaging and behavior 2018-12, Vol.12 (6), p.1650-1657 |
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description | Sleep deprivation (SD) can alter the intrinsic brain functional organization. However, its effects on intrinsic low-frequency connectivity in the whole brain have not been well characterized. In this study, we used voxel-based functional connectivity density (FCD) analysis to investigate the effects of SD on the spontaneous functional organization of the brain. Thirty-seven healthy participants underwent this within-subject crossover functional magnetic resonance imaging (fMRI) study during rested wakefulness (RW) and after 36 h of total sleep deprivation (TSD). Decreased long-/short-range FCDs were observed in the posterior cingulate cortex, precuneus, inferior parietal lobule, dorsolateral prefrontal cortex, dorsomedial prefrontal cortex, and ventromedial prefrontal cortex. Increased long-/short-range FCDs were found in the sensory integration and arousal regulating areas, including the postcentral gyrus, thalamus, superior temporal gyrus, and occipital-temporal cortex. Moreover, a significant negative correlation was found between the short-range FCD of the PCC and the reaction time of Psychomotor Vigilance Task. In the present study, spontaneous functional organization with significant group-wise differences between RW and TSD sessions was identified. Our findings extend our understanding of the neural mechanism of how brain activity is altered in sleep-deprived individuals. |
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However, its effects on intrinsic low-frequency connectivity in the whole brain have not been well characterized. In this study, we used voxel-based functional connectivity density (FCD) analysis to investigate the effects of SD on the spontaneous functional organization of the brain. Thirty-seven healthy participants underwent this within-subject crossover functional magnetic resonance imaging (fMRI) study during rested wakefulness (RW) and after 36 h of total sleep deprivation (TSD). Decreased long-/short-range FCDs were observed in the posterior cingulate cortex, precuneus, inferior parietal lobule, dorsolateral prefrontal cortex, dorsomedial prefrontal cortex, and ventromedial prefrontal cortex. Increased long-/short-range FCDs were found in the sensory integration and arousal regulating areas, including the postcentral gyrus, thalamus, superior temporal gyrus, and occipital-temporal cortex. Moreover, a significant negative correlation was found between the short-range FCD of the PCC and the reaction time of Psychomotor Vigilance Task. In the present study, spontaneous functional organization with significant group-wise differences between RW and TSD sessions was identified. Our findings extend our understanding of the neural mechanism of how brain activity is altered in sleep-deprived individuals.</description><identifier>ISSN: 1931-7557</identifier><identifier>EISSN: 1931-7565</identifier><identifier>DOI: 10.1007/s11682-018-9829-9</identifier><identifier>PMID: 29488149</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Arousal ; Biomedical and Life Sciences ; Biomedicine ; Brain ; Brain - diagnostic imaging ; Brain - physiopathology ; Brain architecture ; Brain Mapping ; Cortex (cingulate) ; Cortex (parietal) ; Functional magnetic resonance imaging ; Functional morphology ; Humans ; Magnetic Resonance Imaging ; Male ; Neural networks ; Neural Pathways - diagnostic imaging ; Neural Pathways - physiopathology ; Neuroimaging ; Neuropsychology ; Neuroradiology ; Neurosciences ; Occipital lobe ; Original Research ; Postcentral gyrus ; Prefrontal cortex ; Psychiatry ; Reaction time ; Reaction time task ; Rest ; Sensory integration ; Sleep and wakefulness ; Sleep deprivation ; Sleep Deprivation - diagnostic imaging ; Sleep Deprivation - physiopathology ; Somatosensory cortex ; Superior temporal gyrus ; Temporal cortex ; Temporal gyrus ; Thalamus ; Vigilance ; Wakefulness ; Young Adult</subject><ispartof>Brain imaging and behavior, 2018-12, Vol.12 (6), p.1650-1657</ispartof><rights>Springer Science+Business Media, LLC, part of Springer Nature 2018</rights><rights>Brain Imaging and Behavior is a copyright of Springer, (2018). All Rights Reserved.</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c372t-8356e0c71cc4d52bab88e9fbd4e489c550ae1b7df5b558d078b2efd34c018fad3</citedby><cites>FETCH-LOGICAL-c372t-8356e0c71cc4d52bab88e9fbd4e489c550ae1b7df5b558d078b2efd34c018fad3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,776,780,27901,27902</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/29488149$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Yang, Liu</creatorcontrib><creatorcontrib>Lei, Yu</creatorcontrib><creatorcontrib>Wang, Lubin</creatorcontrib><creatorcontrib>Chen, Pinhong</creatorcontrib><creatorcontrib>Cheng, Shan</creatorcontrib><creatorcontrib>Chen, Shanshan</creatorcontrib><creatorcontrib>Sun, Jicheng</creatorcontrib><creatorcontrib>Li, Yanyan</creatorcontrib><creatorcontrib>Wang, Yihan</creatorcontrib><creatorcontrib>Hu, Wendong</creatorcontrib><creatorcontrib>Yang, Zheng</creatorcontrib><title>Abnormal functional connectivity density in sleep-deprived subjects</title><title>Brain imaging and behavior</title><addtitle>Brain Imaging and Behavior</addtitle><addtitle>Brain Imaging Behav</addtitle><description>Sleep deprivation (SD) can alter the intrinsic brain functional organization. However, its effects on intrinsic low-frequency connectivity in the whole brain have not been well characterized. In this study, we used voxel-based functional connectivity density (FCD) analysis to investigate the effects of SD on the spontaneous functional organization of the brain. Thirty-seven healthy participants underwent this within-subject crossover functional magnetic resonance imaging (fMRI) study during rested wakefulness (RW) and after 36 h of total sleep deprivation (TSD). Decreased long-/short-range FCDs were observed in the posterior cingulate cortex, precuneus, inferior parietal lobule, dorsolateral prefrontal cortex, dorsomedial prefrontal cortex, and ventromedial prefrontal cortex. Increased long-/short-range FCDs were found in the sensory integration and arousal regulating areas, including the postcentral gyrus, thalamus, superior temporal gyrus, and occipital-temporal cortex. Moreover, a significant negative correlation was found between the short-range FCD of the PCC and the reaction time of Psychomotor Vigilance Task. In the present study, spontaneous functional organization with significant group-wise differences between RW and TSD sessions was identified. Our findings extend our understanding of the neural mechanism of how brain activity is altered in sleep-deprived individuals.</description><subject>Arousal</subject><subject>Biomedical and Life Sciences</subject><subject>Biomedicine</subject><subject>Brain</subject><subject>Brain - diagnostic imaging</subject><subject>Brain - physiopathology</subject><subject>Brain architecture</subject><subject>Brain Mapping</subject><subject>Cortex (cingulate)</subject><subject>Cortex (parietal)</subject><subject>Functional magnetic resonance imaging</subject><subject>Functional morphology</subject><subject>Humans</subject><subject>Magnetic Resonance Imaging</subject><subject>Male</subject><subject>Neural networks</subject><subject>Neural Pathways - diagnostic imaging</subject><subject>Neural Pathways - physiopathology</subject><subject>Neuroimaging</subject><subject>Neuropsychology</subject><subject>Neuroradiology</subject><subject>Neurosciences</subject><subject>Occipital lobe</subject><subject>Original Research</subject><subject>Postcentral gyrus</subject><subject>Prefrontal cortex</subject><subject>Psychiatry</subject><subject>Reaction time</subject><subject>Reaction time task</subject><subject>Rest</subject><subject>Sensory integration</subject><subject>Sleep and wakefulness</subject><subject>Sleep deprivation</subject><subject>Sleep Deprivation - diagnostic imaging</subject><subject>Sleep Deprivation - physiopathology</subject><subject>Somatosensory cortex</subject><subject>Superior temporal gyrus</subject><subject>Temporal cortex</subject><subject>Temporal gyrus</subject><subject>Thalamus</subject><subject>Vigilance</subject><subject>Wakefulness</subject><subject>Young Adult</subject><issn>1931-7557</issn><issn>1931-7565</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><recordid>eNp1kE9LAzEQxYMoVqsfwIssePESTbKbTXIsxX9Q8KLnsElmZctutibdQr-9qVsrCJ5mQn7zZt5D6IqSO0qIuI-UlpJhQiVWkimsjtAZVTnFgpf8-NBzMUHnMS4J4YVU9BRNmCqkpIU6Q_OZ8X3oqjarB2_XTe9Ta3vvIT02zXqbOfBxVxufxRZghR2sQrMBl8XBLBMWL9BJXbURLvd1it4fH97mz3jx-vQyny2wzQVbY5nzEogV1NrCcWYqIyWo2rgC0lmWc1IBNcLV3HAuHRHSMKhdXthksK5cPkW3o-4q9J8DxLXummihbSsP_RA1I0QxWrCSJ_TmD7rsh5C8fVNSkDyXNFF0pGzoYwxQ6-Ssq8JWU6J3CesxYZ0O0LuEtUoz13vlwXTgDhM_kSaAjUBMX_4Dwu_q_1W_ANUhhuU</recordid><startdate>20181201</startdate><enddate>20181201</enddate><creator>Yang, Liu</creator><creator>Lei, Yu</creator><creator>Wang, Lubin</creator><creator>Chen, Pinhong</creator><creator>Cheng, Shan</creator><creator>Chen, Shanshan</creator><creator>Sun, Jicheng</creator><creator>Li, Yanyan</creator><creator>Wang, Yihan</creator><creator>Hu, Wendong</creator><creator>Yang, Zheng</creator><general>Springer US</general><general>Springer Nature B.V</general><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7TK</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FE</scope><scope>8FG</scope><scope>8FH</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>ARAPS</scope><scope>AZQEC</scope><scope>BBNVY</scope><scope>BENPR</scope><scope>BGLVJ</scope><scope>BHPHI</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>HCIFZ</scope><scope>K9.</scope><scope>KB0</scope><scope>LK8</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M7P</scope><scope>NAPCQ</scope><scope>P5Z</scope><scope>P62</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope></search><sort><creationdate>20181201</creationdate><title>Abnormal functional connectivity density in sleep-deprived subjects</title><author>Yang, Liu ; Lei, Yu ; Wang, Lubin ; Chen, Pinhong ; Cheng, Shan ; Chen, Shanshan ; Sun, Jicheng ; Li, Yanyan ; Wang, Yihan ; Hu, Wendong ; Yang, Zheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c372t-8356e0c71cc4d52bab88e9fbd4e489c550ae1b7df5b558d078b2efd34c018fad3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Arousal</topic><topic>Biomedical and Life Sciences</topic><topic>Biomedicine</topic><topic>Brain</topic><topic>Brain - diagnostic imaging</topic><topic>Brain - physiopathology</topic><topic>Brain architecture</topic><topic>Brain Mapping</topic><topic>Cortex (cingulate)</topic><topic>Cortex (parietal)</topic><topic>Functional magnetic resonance imaging</topic><topic>Functional morphology</topic><topic>Humans</topic><topic>Magnetic Resonance Imaging</topic><topic>Male</topic><topic>Neural networks</topic><topic>Neural Pathways - diagnostic imaging</topic><topic>Neural Pathways - physiopathology</topic><topic>Neuroimaging</topic><topic>Neuropsychology</topic><topic>Neuroradiology</topic><topic>Neurosciences</topic><topic>Occipital lobe</topic><topic>Original Research</topic><topic>Postcentral gyrus</topic><topic>Prefrontal cortex</topic><topic>Psychiatry</topic><topic>Reaction time</topic><topic>Reaction time task</topic><topic>Rest</topic><topic>Sensory integration</topic><topic>Sleep and wakefulness</topic><topic>Sleep deprivation</topic><topic>Sleep Deprivation - diagnostic imaging</topic><topic>Sleep Deprivation - physiopathology</topic><topic>Somatosensory cortex</topic><topic>Superior temporal gyrus</topic><topic>Temporal cortex</topic><topic>Temporal gyrus</topic><topic>Thalamus</topic><topic>Vigilance</topic><topic>Wakefulness</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Yang, Liu</creatorcontrib><creatorcontrib>Lei, Yu</creatorcontrib><creatorcontrib>Wang, Lubin</creatorcontrib><creatorcontrib>Chen, Pinhong</creatorcontrib><creatorcontrib>Cheng, Shan</creatorcontrib><creatorcontrib>Chen, Shanshan</creatorcontrib><creatorcontrib>Sun, Jicheng</creatorcontrib><creatorcontrib>Li, Yanyan</creatorcontrib><creatorcontrib>Wang, Yihan</creatorcontrib><creatorcontrib>Hu, Wendong</creatorcontrib><creatorcontrib>Yang, Zheng</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Nursing and Allied Health Journals</collection><collection>Neurosciences Abstracts</collection><collection>Health & Medical Collection (ProQuest Medical & Health Databases)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>ProQuest SciTech Collection</collection><collection>ProQuest Technology Collection</collection><collection>ProQuest Natural Science Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>Advanced Technologies & Aerospace Database (1962 - 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Academic</collection><jtitle>Brain imaging and behavior</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Yang, Liu</au><au>Lei, Yu</au><au>Wang, Lubin</au><au>Chen, Pinhong</au><au>Cheng, Shan</au><au>Chen, Shanshan</au><au>Sun, Jicheng</au><au>Li, Yanyan</au><au>Wang, Yihan</au><au>Hu, Wendong</au><au>Yang, Zheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Abnormal functional connectivity density in sleep-deprived subjects</atitle><jtitle>Brain imaging and behavior</jtitle><stitle>Brain Imaging and Behavior</stitle><addtitle>Brain Imaging Behav</addtitle><date>2018-12-01</date><risdate>2018</risdate><volume>12</volume><issue>6</issue><spage>1650</spage><epage>1657</epage><pages>1650-1657</pages><issn>1931-7557</issn><eissn>1931-7565</eissn><abstract>Sleep deprivation (SD) can alter the intrinsic brain functional organization. However, its effects on intrinsic low-frequency connectivity in the whole brain have not been well characterized. In this study, we used voxel-based functional connectivity density (FCD) analysis to investigate the effects of SD on the spontaneous functional organization of the brain. Thirty-seven healthy participants underwent this within-subject crossover functional magnetic resonance imaging (fMRI) study during rested wakefulness (RW) and after 36 h of total sleep deprivation (TSD). Decreased long-/short-range FCDs were observed in the posterior cingulate cortex, precuneus, inferior parietal lobule, dorsolateral prefrontal cortex, dorsomedial prefrontal cortex, and ventromedial prefrontal cortex. Increased long-/short-range FCDs were found in the sensory integration and arousal regulating areas, including the postcentral gyrus, thalamus, superior temporal gyrus, and occipital-temporal cortex. Moreover, a significant negative correlation was found between the short-range FCD of the PCC and the reaction time of Psychomotor Vigilance Task. In the present study, spontaneous functional organization with significant group-wise differences between RW and TSD sessions was identified. Our findings extend our understanding of the neural mechanism of how brain activity is altered in sleep-deprived individuals.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>29488149</pmid><doi>10.1007/s11682-018-9829-9</doi><tpages>8</tpages></addata></record> |
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subjects | Arousal Biomedical and Life Sciences Biomedicine Brain Brain - diagnostic imaging Brain - physiopathology Brain architecture Brain Mapping Cortex (cingulate) Cortex (parietal) Functional magnetic resonance imaging Functional morphology Humans Magnetic Resonance Imaging Male Neural networks Neural Pathways - diagnostic imaging Neural Pathways - physiopathology Neuroimaging Neuropsychology Neuroradiology Neurosciences Occipital lobe Original Research Postcentral gyrus Prefrontal cortex Psychiatry Reaction time Reaction time task Rest Sensory integration Sleep and wakefulness Sleep deprivation Sleep Deprivation - diagnostic imaging Sleep Deprivation - physiopathology Somatosensory cortex Superior temporal gyrus Temporal cortex Temporal gyrus Thalamus Vigilance Wakefulness Young Adult |
title | Abnormal functional connectivity density in sleep-deprived subjects |
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