Heartbeat-related EEG amplitude and phase modulations from wakefulness to deep sleep: Interactions with sleep spindles and slow oscillations
Based on physiological models of neurovisceral integration, different studies have shown how cognitive processes modulate heart rate and how the heartbeat, on the other hand, modulates brain activity. We tried to further determine interactions between cardiac and electrical brain activity by means o...
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Veröffentlicht in: | Psychophysiology 2015-11, Vol.52 (11), p.1441-1450 |
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description | Based on physiological models of neurovisceral integration, different studies have shown how cognitive processes modulate heart rate and how the heartbeat, on the other hand, modulates brain activity. We tried to further determine interactions between cardiac and electrical brain activity by means of EEG. We investigated how the heartbeat modulates EEG in 23 healthy controls from wakefulness to deep sleep and showed that frontocentral heartbeat evoked EEG amplitude and phase locking (as measured by intertrial phase locking), at about 300‐400 ms after the R peak, decreased with increasing sleep depth with a renewed increase during REM sleep, which underpins the assumption that the heartbeat evoked positivity constitutes an active frontocortical response to the heartbeat. Additionally, we found that individual heart rate was correlated with the frequency of the EEG's spectral peak (i.e., alpha peak frequency during wakefulness). This correlation was strongest during wakefulness and declined linearly with increasing sleep depth. Furthermore, we show that the QRS complex modulates spindle phase possibly related to the correspondence between the frequency of the QRS complex and the spindle frequency of about 12–15 Hz. Finally, during deep sleep stages, a loose temporal coupling between heartbeats and slow oscillation (0.8 Hz) could be observed. These findings indicate that cardiac activity such as heart rate or individual heartbeats can modulate or be modulated by ongoing oscillatory brain activity. |
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We tried to further determine interactions between cardiac and electrical brain activity by means of EEG. We investigated how the heartbeat modulates EEG in 23 healthy controls from wakefulness to deep sleep and showed that frontocentral heartbeat evoked EEG amplitude and phase locking (as measured by intertrial phase locking), at about 300‐400 ms after the R peak, decreased with increasing sleep depth with a renewed increase during REM sleep, which underpins the assumption that the heartbeat evoked positivity constitutes an active frontocortical response to the heartbeat. Additionally, we found that individual heart rate was correlated with the frequency of the EEG's spectral peak (i.e., alpha peak frequency during wakefulness). This correlation was strongest during wakefulness and declined linearly with increasing sleep depth. Furthermore, we show that the QRS complex modulates spindle phase possibly related to the correspondence between the frequency of the QRS complex and the spindle frequency of about 12–15 Hz. Finally, during deep sleep stages, a loose temporal coupling between heartbeats and slow oscillation (0.8 Hz) could be observed. 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Furthermore, we show that the QRS complex modulates spindle phase possibly related to the correspondence between the frequency of the QRS complex and the spindle frequency of about 12–15 Hz. Finally, during deep sleep stages, a loose temporal coupling between heartbeats and slow oscillation (0.8 Hz) could be observed. These findings indicate that cardiac activity such as heart rate or individual heartbeats can modulate or be modulated by ongoing oscillatory brain activity.</description><subject>Brain - physiology</subject><subject>EEG oscillations</subject><subject>Electroencephalography</subject><subject>Female</subject><subject>Heart rate</subject><subject>Heart Rate - physiology</subject><subject>Heartbeat evoked potential</subject><subject>Humans</subject><subject>Male</subject><subject>Neuropsychology</subject><subject>Polysomnography</subject><subject>Sleep</subject><subject>Sleep - physiology</subject><subject>Sleep spindles</subject><subject>Sleep Stages - physiology</subject><subject>Slow oscillations</subject><subject>Wakefulness - physiology</subject><issn>0048-5772</issn><issn>1469-8986</issn><issn>1540-5958</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2015</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kU1v1DAQhi0EoqVw4QcgS1wQUortxF_cqmW7rbQqlfgSJ8trT9S0SRzsRMv-B3407mbbAwfmMHOYZx6N9CL0mpJTmuvDkHbDKWWcqCfomFZCF0or8RQdE1KpgkvJjtCLlG4JIZoy9hwdMcGEUlwdoz8XYOO4ATsWEVo7gsfL5QrbbmibcfKAbe_xcGMT4C74KRNN6BOuY-jw1t5BPbU9pITHgD3AgFOb-0d82Y8QrZvhbTPezAuchqb3LaS9NrVhi0NyTXvQvkTPatsmeHWYJ-jb-fLr4qJYf15dLs7WhasEV8VG6rr00jHqaE1BiYpy7bivONSKykoLTyR3XkFthbKVVrJ0vNzUUjBCmShP0LvZO8Twa4I0mq5JDvIbPYQpGSqp1jI3ltG3_6C3YYp9_m5P0azWMlPvZ8rFkFKE2gyx6WzcGUrMfUbmPiOzzyjDbw7KadOBf0QfQskAnYFt08LuPypz_eXn9YO0mG-aNMLvxxsb74yQpeTmx9XKlFfn8tNivTDfy788e61p</recordid><startdate>201511</startdate><enddate>201511</enddate><creator>Lechinger, Julia</creator><creator>Heib, Dominik Philip Johannes</creator><creator>Gruber, Walter</creator><creator>Schabus, Manuel</creator><creator>Klimesch, Wolfgang</creator><general>Blackwell Publishing Ltd</general><scope>BSCLL</scope><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>7TK</scope><scope>K9.</scope><scope>7X8</scope></search><sort><creationdate>201511</creationdate><title>Heartbeat-related EEG amplitude and phase modulations from wakefulness to deep sleep: Interactions with sleep spindles and slow oscillations</title><author>Lechinger, Julia ; Heib, Dominik Philip Johannes ; Gruber, Walter ; Schabus, Manuel ; Klimesch, Wolfgang</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4658-b79f3d7c21c1f1e864159c5d45ef817496d075cd8efa68a49873c53bf76201263</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2015</creationdate><topic>Brain - physiology</topic><topic>EEG oscillations</topic><topic>Electroencephalography</topic><topic>Female</topic><topic>Heart rate</topic><topic>Heart Rate - physiology</topic><topic>Heartbeat evoked potential</topic><topic>Humans</topic><topic>Male</topic><topic>Neuropsychology</topic><topic>Polysomnography</topic><topic>Sleep</topic><topic>Sleep - physiology</topic><topic>Sleep spindles</topic><topic>Sleep Stages - physiology</topic><topic>Slow oscillations</topic><topic>Wakefulness - physiology</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Lechinger, Julia</creatorcontrib><creatorcontrib>Heib, Dominik Philip Johannes</creatorcontrib><creatorcontrib>Gruber, Walter</creatorcontrib><creatorcontrib>Schabus, Manuel</creatorcontrib><creatorcontrib>Klimesch, Wolfgang</creatorcontrib><collection>Istex</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>Neurosciences Abstracts</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>MEDLINE - Academic</collection><jtitle>Psychophysiology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Lechinger, Julia</au><au>Heib, Dominik Philip Johannes</au><au>Gruber, Walter</au><au>Schabus, Manuel</au><au>Klimesch, Wolfgang</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Heartbeat-related EEG amplitude and phase modulations from wakefulness to deep sleep: Interactions with sleep spindles and slow oscillations</atitle><jtitle>Psychophysiology</jtitle><addtitle>Psychophysiol</addtitle><date>2015-11</date><risdate>2015</risdate><volume>52</volume><issue>11</issue><spage>1441</spage><epage>1450</epage><pages>1441-1450</pages><issn>0048-5772</issn><eissn>1469-8986</eissn><eissn>1540-5958</eissn><abstract>Based on physiological models of neurovisceral integration, different studies have shown how cognitive processes modulate heart rate and how the heartbeat, on the other hand, modulates brain activity. We tried to further determine interactions between cardiac and electrical brain activity by means of EEG. We investigated how the heartbeat modulates EEG in 23 healthy controls from wakefulness to deep sleep and showed that frontocentral heartbeat evoked EEG amplitude and phase locking (as measured by intertrial phase locking), at about 300‐400 ms after the R peak, decreased with increasing sleep depth with a renewed increase during REM sleep, which underpins the assumption that the heartbeat evoked positivity constitutes an active frontocortical response to the heartbeat. Additionally, we found that individual heart rate was correlated with the frequency of the EEG's spectral peak (i.e., alpha peak frequency during wakefulness). This correlation was strongest during wakefulness and declined linearly with increasing sleep depth. Furthermore, we show that the QRS complex modulates spindle phase possibly related to the correspondence between the frequency of the QRS complex and the spindle frequency of about 12–15 Hz. Finally, during deep sleep stages, a loose temporal coupling between heartbeats and slow oscillation (0.8 Hz) could be observed. These findings indicate that cardiac activity such as heart rate or individual heartbeats can modulate or be modulated by ongoing oscillatory brain activity.</abstract><cop>United States</cop><pub>Blackwell Publishing Ltd</pub><pmid>26268858</pmid><doi>10.1111/psyp.12508</doi><tpages>10</tpages></addata></record> |
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subjects | Brain - physiology EEG oscillations Electroencephalography Female Heart rate Heart Rate - physiology Heartbeat evoked potential Humans Male Neuropsychology Polysomnography Sleep Sleep - physiology Sleep spindles Sleep Stages - physiology Slow oscillations Wakefulness - physiology |
title | Heartbeat-related EEG amplitude and phase modulations from wakefulness to deep sleep: Interactions with sleep spindles and slow oscillations |
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