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0419 HEMISPHERIC AND MORPHOLOGICAL CHARACTERISTICS OF SLEEP SPINDLES IN PRIMARY INSOMNIA AND GOOD SLEEPERS
Abstract Introduction: Sleep spindles are implicated in memory consolidation and possibly altered in psychopathology. However, little is known about quantitative and morphological abnormalities in Primary Insomnia (PI). We explored differences in sleep spindle characteristics between PI and Good Sle...
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Published in: | Sleep (New York, N.Y.) N.Y.), 2017-04, Vol.40 (suppl_1), p.A155-A155 |
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creator | Gazecki, S Bottary, RM Purcell, S Moore, KN Lasko, NB Milad, MR Pace-Schott, EF |
description | Abstract
Introduction:
Sleep spindles are implicated in memory consolidation and possibly altered in psychopathology. However, little is known about quantitative and morphological abnormalities in Primary Insomnia (PI). We explored differences in sleep spindle characteristics between PI and Good Sleepers (GS).
Methods:
Following an acclimation night, 23 PI (16 female, Age: M=21.3, SD=14.3yrs) and 19 GS (14 female, Age: M=32.6, SD=14.9yrs) completed consecutive nights of home sleep monitoring (psg-2 and psg-3) prior to a fear conditioning and extinction task. Signal processing of artifact free scalp EEG was accomplished using co-author S.P’s open source C/C++ program (http://zzz.bwh.harvard.edu). Canonical (13.5Hz), fast (15Hz), and slow (11Hz), spindles were detected from bilateral central (C3, C4; canonical and fast) and frontal (F3, F4; slow) derivations using wavelet analysis with adaptive thresholds. Spindle Amplitude, Density and Duration were calculated for detected spindles. For canonical, fast and slow spindle frequency types, two-group (PI vs. GS) x 2 Night (psg-2 vs. psg-3) x 2 Hemisphere (left vs. right) ANOVAs for Amplitude, Density and Duration were conducted independently for stages N2 and N3.
Results:
For canonical spindles, we observed a Hemisphere main effect for N2 Density (left > right, F(1,20) =6.750,p =.017), a main effect trend of Night for N2 Amplitude (night 3>night2, F(1,20)=3.803,p=.065) and Hemisphere for N3 Amplitude (left>right, F(1,20)=4.325,p=.052), and a trend for a Night x Hemisphere interaction for N3 Duration (F(1,20)=3.458,p =.078). For fast spindles, we observed a main effect of Night for N2 Amplitude (psg 3>psg 2, F(1,20)=6.272,p =.021), Group for N3 Duration (PI>GS,F(1,20)=6.107, p=.024), and a Night x Hemisphere interaction trend for Duration (F(1,20)=3.510,p =.077). For slow spindles, we observed a main effect of Group for N2 Duration (PI>GS,F(1,20)=6.460,p=.019) and main effect trend of night for N2 Amplitude (psg3>psg2, F(1,20)=3.258,p=.085) and group for N3 duration (PI>GS,F(1,20)=3.542,p=.075).
Conclusion:
Hemispheric differences in N2 canonical spindle density is conserved in both PI and GS. N2 fast spindles’ Amplitude increased from psg-2 to psg-3, possibly influenced by task-related learning. Compared to GS, PI demonstrated greater spindle duration for fast spindles in N3 and slow spindles in N2, offering a possible signature for the condition.
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R21MH101567. |
doi_str_mv | 10.1093/sleepj/zsx050.418 |
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Introduction:
Sleep spindles are implicated in memory consolidation and possibly altered in psychopathology. However, little is known about quantitative and morphological abnormalities in Primary Insomnia (PI). We explored differences in sleep spindle characteristics between PI and Good Sleepers (GS).
Methods:
Following an acclimation night, 23 PI (16 female, Age: M=21.3, SD=14.3yrs) and 19 GS (14 female, Age: M=32.6, SD=14.9yrs) completed consecutive nights of home sleep monitoring (psg-2 and psg-3) prior to a fear conditioning and extinction task. Signal processing of artifact free scalp EEG was accomplished using co-author S.P’s open source C/C++ program (http://zzz.bwh.harvard.edu). Canonical (13.5Hz), fast (15Hz), and slow (11Hz), spindles were detected from bilateral central (C3, C4; canonical and fast) and frontal (F3, F4; slow) derivations using wavelet analysis with adaptive thresholds. Spindle Amplitude, Density and Duration were calculated for detected spindles. For canonical, fast and slow spindle frequency types, two-group (PI vs. GS) x 2 Night (psg-2 vs. psg-3) x 2 Hemisphere (left vs. right) ANOVAs for Amplitude, Density and Duration were conducted independently for stages N2 and N3.
Results:
For canonical spindles, we observed a Hemisphere main effect for N2 Density (left > right, F(1,20) =6.750,p =.017), a main effect trend of Night for N2 Amplitude (night 3>night2, F(1,20)=3.803,p=.065) and Hemisphere for N3 Amplitude (left>right, F(1,20)=4.325,p=.052), and a trend for a Night x Hemisphere interaction for N3 Duration (F(1,20)=3.458,p =.078). For fast spindles, we observed a main effect of Night for N2 Amplitude (psg 3>psg 2, F(1,20)=6.272,p =.021), Group for N3 Duration (PI>GS,F(1,20)=6.107, p=.024), and a Night x Hemisphere interaction trend for Duration (F(1,20)=3.510,p =.077). For slow spindles, we observed a main effect of Group for N2 Duration (PI>GS,F(1,20)=6.460,p=.019) and main effect trend of night for N2 Amplitude (psg3>psg2, F(1,20)=3.258,p=.085) and group for N3 duration (PI>GS,F(1,20)=3.542,p=.075).
Conclusion:
Hemispheric differences in N2 canonical spindle density is conserved in both PI and GS. N2 fast spindles’ Amplitude increased from psg-2 to psg-3, possibly influenced by task-related learning. Compared to GS, PI demonstrated greater spindle duration for fast spindles in N3 and slow spindles in N2, offering a possible signature for the condition.
Support (If Any):
R21MH101567.</description><identifier>ISSN: 0161-8105</identifier><identifier>EISSN: 1550-9109</identifier><identifier>DOI: 10.1093/sleepj/zsx050.418</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Insomnia ; Morphology ; Sleep</subject><ispartof>Sleep (New York, N.Y.), 2017-04, Vol.40 (suppl_1), p.A155-A155</ispartof><rights>Sleep Research Society 2017. Published by Oxford University Press [on behalf of the Sleep Research Society]. All rights reserved. For permissions, please email: journals.permissions@oup.com 2017</rights><rights>Sleep Research Society 2017. Published by Oxford University Press [on behalf of the Sleep Research Society]. All rights reserved. For permissions, please email: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,777,781,27905,27906</link.rule.ids></links><search><creatorcontrib>Gazecki, S</creatorcontrib><creatorcontrib>Bottary, RM</creatorcontrib><creatorcontrib>Purcell, S</creatorcontrib><creatorcontrib>Moore, KN</creatorcontrib><creatorcontrib>Lasko, NB</creatorcontrib><creatorcontrib>Milad, MR</creatorcontrib><creatorcontrib>Pace-Schott, EF</creatorcontrib><title>0419 HEMISPHERIC AND MORPHOLOGICAL CHARACTERISTICS OF SLEEP SPINDLES IN PRIMARY INSOMNIA AND GOOD SLEEPERS</title><title>Sleep (New York, N.Y.)</title><description>Abstract
Introduction:
Sleep spindles are implicated in memory consolidation and possibly altered in psychopathology. However, little is known about quantitative and morphological abnormalities in Primary Insomnia (PI). We explored differences in sleep spindle characteristics between PI and Good Sleepers (GS).
Methods:
Following an acclimation night, 23 PI (16 female, Age: M=21.3, SD=14.3yrs) and 19 GS (14 female, Age: M=32.6, SD=14.9yrs) completed consecutive nights of home sleep monitoring (psg-2 and psg-3) prior to a fear conditioning and extinction task. Signal processing of artifact free scalp EEG was accomplished using co-author S.P’s open source C/C++ program (http://zzz.bwh.harvard.edu). Canonical (13.5Hz), fast (15Hz), and slow (11Hz), spindles were detected from bilateral central (C3, C4; canonical and fast) and frontal (F3, F4; slow) derivations using wavelet analysis with adaptive thresholds. Spindle Amplitude, Density and Duration were calculated for detected spindles. For canonical, fast and slow spindle frequency types, two-group (PI vs. GS) x 2 Night (psg-2 vs. psg-3) x 2 Hemisphere (left vs. right) ANOVAs for Amplitude, Density and Duration were conducted independently for stages N2 and N3.
Results:
For canonical spindles, we observed a Hemisphere main effect for N2 Density (left > right, F(1,20) =6.750,p =.017), a main effect trend of Night for N2 Amplitude (night 3>night2, F(1,20)=3.803,p=.065) and Hemisphere for N3 Amplitude (left>right, F(1,20)=4.325,p=.052), and a trend for a Night x Hemisphere interaction for N3 Duration (F(1,20)=3.458,p =.078). For fast spindles, we observed a main effect of Night for N2 Amplitude (psg 3>psg 2, F(1,20)=6.272,p =.021), Group for N3 Duration (PI>GS,F(1,20)=6.107, p=.024), and a Night x Hemisphere interaction trend for Duration (F(1,20)=3.510,p =.077). For slow spindles, we observed a main effect of Group for N2 Duration (PI>GS,F(1,20)=6.460,p=.019) and main effect trend of night for N2 Amplitude (psg3>psg2, F(1,20)=3.258,p=.085) and group for N3 duration (PI>GS,F(1,20)=3.542,p=.075).
Conclusion:
Hemispheric differences in N2 canonical spindle density is conserved in both PI and GS. N2 fast spindles’ Amplitude increased from psg-2 to psg-3, possibly influenced by task-related learning. Compared to GS, PI demonstrated greater spindle duration for fast spindles in N3 and slow spindles in N2, offering a possible signature for the condition.
Support (If Any):
R21MH101567.</description><subject>Insomnia</subject><subject>Morphology</subject><subject>Sleep</subject><issn>0161-8105</issn><issn>1550-9109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2017</creationdate><recordtype>article</recordtype><recordid>eNqNkM1OwzAQhC0EEqXwANwscSXFm9iJfYzStLGUPyXlwMkyiSMRFVISKgFPjyF9AE67q5nZkT6EboGsgAjvYdobc-gfvqdPwsiKAj9DC2CMOMLK52hBwAeHA2GX6GqaemJvKrwF6gkFgZM4k3WZxJWMcJivcVZUZVKkxVZGYYqjJKzCaGfVeiejGhcbXKdxXOK6lPk6jWssc1xWMgurJ7vWRZbL8O_PtijWszeu6mt00en9ZG5Oc4keN_EuSpxTj9MAI9wJRGsEp5p5XQCNoIYGnTBtq5kA7vNW-z4jGlgLwHRnOkPdjnj8mTRac-OCt0R389_DOLwfzfSh-uE4vtlK5TLiUQoQuNYFs6sZh2kaTacO48urHr8UEPWLVM1I1YxUWaQ2cz9nhuPhH_YfxGpx0w</recordid><startdate>20170428</startdate><enddate>20170428</enddate><creator>Gazecki, S</creator><creator>Bottary, RM</creator><creator>Purcell, S</creator><creator>Moore, KN</creator><creator>Lasko, NB</creator><creator>Milad, MR</creator><creator>Pace-Schott, EF</creator><general>Oxford University Press</general><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>88G</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>K9.</scope><scope>M0S</scope><scope>M1P</scope><scope>M2M</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PSYQQ</scope><scope>Q9U</scope></search><sort><creationdate>20170428</creationdate><title>0419 HEMISPHERIC AND MORPHOLOGICAL CHARACTERISTICS OF SLEEP SPINDLES IN PRIMARY INSOMNIA AND GOOD SLEEPERS</title><author>Gazecki, S ; Bottary, RM ; Purcell, S ; Moore, KN ; Lasko, NB ; Milad, MR ; Pace-Schott, EF</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c1508-79de984a53f71c94e47f9edda591868da6650a15d115afefe42f038b0caa8e213</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2017</creationdate><topic>Insomnia</topic><topic>Morphology</topic><topic>Sleep</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gazecki, S</creatorcontrib><creatorcontrib>Bottary, RM</creatorcontrib><creatorcontrib>Purcell, S</creatorcontrib><creatorcontrib>Moore, KN</creatorcontrib><creatorcontrib>Lasko, NB</creatorcontrib><creatorcontrib>Milad, MR</creatorcontrib><creatorcontrib>Pace-Schott, EF</creatorcontrib><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest - Health & Medical Complete保健、医学与药学数据库</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>Psychology Database (Alumni)</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>AUTh Library subscriptions: ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>PML(ProQuest Medical Library)</collection><collection>Psychology Database (ProQuest)</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><jtitle>Sleep (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gazecki, S</au><au>Bottary, RM</au><au>Purcell, S</au><au>Moore, KN</au><au>Lasko, NB</au><au>Milad, MR</au><au>Pace-Schott, EF</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>0419 HEMISPHERIC AND MORPHOLOGICAL CHARACTERISTICS OF SLEEP SPINDLES IN PRIMARY INSOMNIA AND GOOD SLEEPERS</atitle><jtitle>Sleep (New York, N.Y.)</jtitle><date>2017-04-28</date><risdate>2017</risdate><volume>40</volume><issue>suppl_1</issue><spage>A155</spage><epage>A155</epage><pages>A155-A155</pages><issn>0161-8105</issn><eissn>1550-9109</eissn><abstract>Abstract
Introduction:
Sleep spindles are implicated in memory consolidation and possibly altered in psychopathology. However, little is known about quantitative and morphological abnormalities in Primary Insomnia (PI). We explored differences in sleep spindle characteristics between PI and Good Sleepers (GS).
Methods:
Following an acclimation night, 23 PI (16 female, Age: M=21.3, SD=14.3yrs) and 19 GS (14 female, Age: M=32.6, SD=14.9yrs) completed consecutive nights of home sleep monitoring (psg-2 and psg-3) prior to a fear conditioning and extinction task. Signal processing of artifact free scalp EEG was accomplished using co-author S.P’s open source C/C++ program (http://zzz.bwh.harvard.edu). Canonical (13.5Hz), fast (15Hz), and slow (11Hz), spindles were detected from bilateral central (C3, C4; canonical and fast) and frontal (F3, F4; slow) derivations using wavelet analysis with adaptive thresholds. Spindle Amplitude, Density and Duration were calculated for detected spindles. For canonical, fast and slow spindle frequency types, two-group (PI vs. GS) x 2 Night (psg-2 vs. psg-3) x 2 Hemisphere (left vs. right) ANOVAs for Amplitude, Density and Duration were conducted independently for stages N2 and N3.
Results:
For canonical spindles, we observed a Hemisphere main effect for N2 Density (left > right, F(1,20) =6.750,p =.017), a main effect trend of Night for N2 Amplitude (night 3>night2, F(1,20)=3.803,p=.065) and Hemisphere for N3 Amplitude (left>right, F(1,20)=4.325,p=.052), and a trend for a Night x Hemisphere interaction for N3 Duration (F(1,20)=3.458,p =.078). For fast spindles, we observed a main effect of Night for N2 Amplitude (psg 3>psg 2, F(1,20)=6.272,p =.021), Group for N3 Duration (PI>GS,F(1,20)=6.107, p=.024), and a Night x Hemisphere interaction trend for Duration (F(1,20)=3.510,p =.077). For slow spindles, we observed a main effect of Group for N2 Duration (PI>GS,F(1,20)=6.460,p=.019) and main effect trend of night for N2 Amplitude (psg3>psg2, F(1,20)=3.258,p=.085) and group for N3 duration (PI>GS,F(1,20)=3.542,p=.075).
Conclusion:
Hemispheric differences in N2 canonical spindle density is conserved in both PI and GS. N2 fast spindles’ Amplitude increased from psg-2 to psg-3, possibly influenced by task-related learning. Compared to GS, PI demonstrated greater spindle duration for fast spindles in N3 and slow spindles in N2, offering a possible signature for the condition.
Support (If Any):
R21MH101567.</abstract><cop>US</cop><pub>Oxford University Press</pub><doi>10.1093/sleepj/zsx050.418</doi><oa>free_for_read</oa></addata></record> |
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subjects | Insomnia Morphology Sleep |
title | 0419 HEMISPHERIC AND MORPHOLOGICAL CHARACTERISTICS OF SLEEP SPINDLES IN PRIMARY INSOMNIA AND GOOD SLEEPERS |
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