Effects of emerging alcohol use on developmental trajectories of functional sleep measures in adolescents
Abstract Study Objectives Adolescence is characterized by significant brain development, accompanied by changes in sleep timing and architecture. It also is a period of profound psychosocial changes, including the initiation of alcohol use; however, it is unknown how alcohol use affects sleep archit...
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| Veröffentlicht in: | Sleep (New York, N.Y.) N.Y.), 2023-09, Vol.46 (9), p.1 |
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| creator | Kiss, Orsolya Goldstone, Aimée de Zambotti, Massimiliano Yüksel, Dilara Hasler, Brant P Franzen, Peter L Brown, Sandra A De Bellis, Michael D Nagel, Bonnie J Nooner, Kate B Tapert, Susan F Colrain, Ian M Clark, Duncan B Baker, Fiona C |
| description | Abstract
Study Objectives
Adolescence is characterized by significant brain development, accompanied by changes in sleep timing and architecture. It also is a period of profound psychosocial changes, including the initiation of alcohol use; however, it is unknown how alcohol use affects sleep architecture in the context of adolescent development. We tracked developmental changes in polysomnographic (PSG) and electroencephalographic (EEG) sleep measures and their relationship with emergent alcohol use in adolescents considering confounding effects (e.g. cannabis use).
Methods
Adolescents (n = 94, 43% female, age: 12–21 years) in the National Consortium on Alcohol and Neurodevelopment in Adolescence (NCANDA) study had annual laboratory PSG recordings across 4-years. Participants were no/low drinkers at baseline.
Results
Linear mixed effect models showed developmental changes in sleep macrostructure and EEG, including a decrease in slow wave sleep and slow wave (delta) EEG activity with advancing age. Emergent moderate/heavy alcohol use across three follow-up years was associated with a decline in percentage rapid eye movement (REM) sleep over time, a longer sleep onset latency (SOL) and shorter total sleep time (TST) in older adolescents, and lower non-REM delta and theta power in males.
Conclusions
These longitudinal data show substantial developmental changes in sleep architecture. Emergent alcohol use during this period was associated with altered sleep continuity, architecture, and EEG measures, with some effects dependent on age and sex. These effects, in part, could be attributed to the effects of alcohol on underlying brain maturation processes involved in sleep–wake regulation.
Graphical Abstract |
| doi_str_mv | 10.1093/sleep/zsad113 |
| format | Article |
| fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10848227</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A765796482</galeid><oup_id>10.1093/sleep/zsad113</oup_id><sourcerecordid>A765796482</sourcerecordid><originalsourceid>FETCH-LOGICAL-c472t-a99666dc6ec933cdb1e66d40751652314565ccf6424885f910dee7123cd6cbe83</originalsourceid><addsrcrecordid>eNqFUk1r3DAQFaWl2aY99loEvfTiRLIs2T6VENIPCPSSnIVWHm20yJIr2YH213d2s02aECg6iNG890ZvZgh5z9kJZ704LQFgOv1dzMC5eEFWXEpW9Zh6SVaMK151nMkj8qaULcO46cVrciRaJjvF2Yr4C-fAzoUmR2GEvPFxQ02w6SYFuhSgKdIBbiGkaYQ4m0DnbLbISNnDnuWWaGefIqb2f6EjmLJkTPpIzZACFIvM8pa8ciYUeHe4j8n1l4ur82_V5Y-v38_PLivbtPVcmb5XSg1Wge2FsMOaA4YNayVXsha8kUpa61RTN10nHTodAFpeI1TZNXTimHy-052W9QjDrnY2QU_Zjyb_0sl4_TgT_Y3epFvNWdd0dd2iwqeDQk4_FyizHj16CMFESEvRdcd43_ZKcoR-fALdpiVjL4oWTAqcBRPtA2pjAmgfXcLCdieqz1olUQoLI-rkGRSeAUZvUwTn8f0Roboj2JxKyeDuTXKmd8uh9wPRh-VA_Id_O3OP_rsND8bTMv1H6w-oH8XJ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>3053550037</pqid></control><display><type>article</type><title>Effects of emerging alcohol use on developmental trajectories of functional sleep measures in adolescents</title><source>MEDLINE</source><source>Oxford University Press Journals All Titles (1996-Current)</source><source>EZB-FREE-00999 freely available EZB journals</source><source>Alma/SFX Local Collection</source><creator>Kiss, Orsolya ; Goldstone, Aimée ; de Zambotti, Massimiliano ; Yüksel, Dilara ; Hasler, Brant P ; Franzen, Peter L ; Brown, Sandra A ; De Bellis, Michael D ; Nagel, Bonnie J ; Nooner, Kate B ; Tapert, Susan F ; Colrain, Ian M ; Clark, Duncan B ; Baker, Fiona C</creator><creatorcontrib>Kiss, Orsolya ; Goldstone, Aimée ; de Zambotti, Massimiliano ; Yüksel, Dilara ; Hasler, Brant P ; Franzen, Peter L ; Brown, Sandra A ; De Bellis, Michael D ; Nagel, Bonnie J ; Nooner, Kate B ; Tapert, Susan F ; Colrain, Ian M ; Clark, Duncan B ; Baker, Fiona C</creatorcontrib><description>Abstract
Study Objectives
Adolescence is characterized by significant brain development, accompanied by changes in sleep timing and architecture. It also is a period of profound psychosocial changes, including the initiation of alcohol use; however, it is unknown how alcohol use affects sleep architecture in the context of adolescent development. We tracked developmental changes in polysomnographic (PSG) and electroencephalographic (EEG) sleep measures and their relationship with emergent alcohol use in adolescents considering confounding effects (e.g. cannabis use).
Methods
Adolescents (n = 94, 43% female, age: 12–21 years) in the National Consortium on Alcohol and Neurodevelopment in Adolescence (NCANDA) study had annual laboratory PSG recordings across 4-years. Participants were no/low drinkers at baseline.
Results
Linear mixed effect models showed developmental changes in sleep macrostructure and EEG, including a decrease in slow wave sleep and slow wave (delta) EEG activity with advancing age. Emergent moderate/heavy alcohol use across three follow-up years was associated with a decline in percentage rapid eye movement (REM) sleep over time, a longer sleep onset latency (SOL) and shorter total sleep time (TST) in older adolescents, and lower non-REM delta and theta power in males.
Conclusions
These longitudinal data show substantial developmental changes in sleep architecture. Emergent alcohol use during this period was associated with altered sleep continuity, architecture, and EEG measures, with some effects dependent on age and sex. These effects, in part, could be attributed to the effects of alcohol on underlying brain maturation processes involved in sleep–wake regulation.
Graphical Abstract</description><identifier>ISSN: 0161-8105</identifier><identifier>EISSN: 1550-9109</identifier><identifier>DOI: 10.1093/sleep/zsad113</identifier><identifier>PMID: 37058610</identifier><language>eng</language><publisher>US: Oxford University Press</publisher><subject>Adolescent ; Adult ; Alcohol and youth ; Alcohol use ; Analysis ; Child ; Child development ; Drinking of alcoholic beverages ; Electroencephalography ; Ethanol ; Female ; Humans ; Male ; Marijuana ; Polysomnography ; REM sleep ; Sleep ; Sleep - physiology ; Sleep Across the Lifespan ; Sleep, REM - physiology ; Sleep, Slow-Wave ; Teenagers ; Young Adult ; Youth</subject><ispartof>Sleep (New York, N.Y.), 2023-09, Vol.46 (9), p.1</ispartof><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Sleep Research Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com 2023</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Sleep Research Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com.</rights><rights>COPYRIGHT 2023 Oxford University Press</rights><rights>The Author(s) 2023. Published by Oxford University Press on behalf of Sleep Research Society. All rights reserved. For permissions, please e-mail: journals.permissions@oup.com</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c472t-a99666dc6ec933cdb1e66d40751652314565ccf6424885f910dee7123cd6cbe83</cites><orcidid>0000-0002-3123-1106 ; 0000-0001-9602-6165 ; 0000-0003-2643-773X ; 0000-0002-0057-5977</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>230,314,780,784,885,1583,27915,27916</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/37058610$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Kiss, Orsolya</creatorcontrib><creatorcontrib>Goldstone, Aimée</creatorcontrib><creatorcontrib>de Zambotti, Massimiliano</creatorcontrib><creatorcontrib>Yüksel, Dilara</creatorcontrib><creatorcontrib>Hasler, Brant P</creatorcontrib><creatorcontrib>Franzen, Peter L</creatorcontrib><creatorcontrib>Brown, Sandra A</creatorcontrib><creatorcontrib>De Bellis, Michael D</creatorcontrib><creatorcontrib>Nagel, Bonnie J</creatorcontrib><creatorcontrib>Nooner, Kate B</creatorcontrib><creatorcontrib>Tapert, Susan F</creatorcontrib><creatorcontrib>Colrain, Ian M</creatorcontrib><creatorcontrib>Clark, Duncan B</creatorcontrib><creatorcontrib>Baker, Fiona C</creatorcontrib><title>Effects of emerging alcohol use on developmental trajectories of functional sleep measures in adolescents</title><title>Sleep (New York, N.Y.)</title><addtitle>Sleep</addtitle><description>Abstract
Study Objectives
Adolescence is characterized by significant brain development, accompanied by changes in sleep timing and architecture. It also is a period of profound psychosocial changes, including the initiation of alcohol use; however, it is unknown how alcohol use affects sleep architecture in the context of adolescent development. We tracked developmental changes in polysomnographic (PSG) and electroencephalographic (EEG) sleep measures and their relationship with emergent alcohol use in adolescents considering confounding effects (e.g. cannabis use).
Methods
Adolescents (n = 94, 43% female, age: 12–21 years) in the National Consortium on Alcohol and Neurodevelopment in Adolescence (NCANDA) study had annual laboratory PSG recordings across 4-years. Participants were no/low drinkers at baseline.
Results
Linear mixed effect models showed developmental changes in sleep macrostructure and EEG, including a decrease in slow wave sleep and slow wave (delta) EEG activity with advancing age. Emergent moderate/heavy alcohol use across three follow-up years was associated with a decline in percentage rapid eye movement (REM) sleep over time, a longer sleep onset latency (SOL) and shorter total sleep time (TST) in older adolescents, and lower non-REM delta and theta power in males.
Conclusions
These longitudinal data show substantial developmental changes in sleep architecture. Emergent alcohol use during this period was associated with altered sleep continuity, architecture, and EEG measures, with some effects dependent on age and sex. These effects, in part, could be attributed to the effects of alcohol on underlying brain maturation processes involved in sleep–wake regulation.
Graphical Abstract</description><subject>Adolescent</subject><subject>Adult</subject><subject>Alcohol and youth</subject><subject>Alcohol use</subject><subject>Analysis</subject><subject>Child</subject><subject>Child development</subject><subject>Drinking of alcoholic beverages</subject><subject>Electroencephalography</subject><subject>Ethanol</subject><subject>Female</subject><subject>Humans</subject><subject>Male</subject><subject>Marijuana</subject><subject>Polysomnography</subject><subject>REM sleep</subject><subject>Sleep</subject><subject>Sleep - physiology</subject><subject>Sleep Across the Lifespan</subject><subject>Sleep, REM - physiology</subject><subject>Sleep, Slow-Wave</subject><subject>Teenagers</subject><subject>Young Adult</subject><subject>Youth</subject><issn>0161-8105</issn><issn>1550-9109</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>8G5</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><sourceid>DWQXO</sourceid><sourceid>GNUQQ</sourceid><sourceid>GUQSH</sourceid><sourceid>M2O</sourceid><recordid>eNqFUk1r3DAQFaWl2aY99loEvfTiRLIs2T6VENIPCPSSnIVWHm20yJIr2YH213d2s02aECg6iNG890ZvZgh5z9kJZ704LQFgOv1dzMC5eEFWXEpW9Zh6SVaMK151nMkj8qaULcO46cVrciRaJjvF2Yr4C-fAzoUmR2GEvPFxQ02w6SYFuhSgKdIBbiGkaYQ4m0DnbLbISNnDnuWWaGefIqb2f6EjmLJkTPpIzZACFIvM8pa8ciYUeHe4j8n1l4ur82_V5Y-v38_PLivbtPVcmb5XSg1Wge2FsMOaA4YNayVXsha8kUpa61RTN10nHTodAFpeI1TZNXTimHy-052W9QjDrnY2QU_Zjyb_0sl4_TgT_Y3epFvNWdd0dd2iwqeDQk4_FyizHj16CMFESEvRdcd43_ZKcoR-fALdpiVjL4oWTAqcBRPtA2pjAmgfXcLCdieqz1olUQoLI-rkGRSeAUZvUwTn8f0Roboj2JxKyeDuTXKmd8uh9wPRh-VA_Id_O3OP_rsND8bTMv1H6w-oH8XJ</recordid><startdate>20230908</startdate><enddate>20230908</enddate><creator>Kiss, Orsolya</creator><creator>Goldstone, Aimée</creator><creator>de Zambotti, Massimiliano</creator><creator>Yüksel, Dilara</creator><creator>Hasler, Brant P</creator><creator>Franzen, Peter L</creator><creator>Brown, Sandra A</creator><creator>De Bellis, Michael D</creator><creator>Nagel, Bonnie J</creator><creator>Nooner, Kate B</creator><creator>Tapert, Susan F</creator><creator>Colrain, Ian M</creator><creator>Clark, Duncan B</creator><creator>Baker, Fiona C</creator><general>Oxford University Press</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>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>PRINS</scope><scope>PSYQQ</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0002-3123-1106</orcidid><orcidid>https://orcid.org/0000-0001-9602-6165</orcidid><orcidid>https://orcid.org/0000-0003-2643-773X</orcidid><orcidid>https://orcid.org/0000-0002-0057-5977</orcidid></search><sort><creationdate>20230908</creationdate><title>Effects of emerging alcohol use on developmental trajectories of functional sleep measures in adolescents</title><author>Kiss, Orsolya ; Goldstone, Aimée ; de Zambotti, Massimiliano ; Yüksel, Dilara ; Hasler, Brant P ; Franzen, Peter L ; Brown, Sandra A ; De Bellis, Michael D ; Nagel, Bonnie J ; Nooner, Kate B ; Tapert, Susan F ; Colrain, Ian M ; Clark, Duncan B ; Baker, Fiona C</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c472t-a99666dc6ec933cdb1e66d40751652314565ccf6424885f910dee7123cd6cbe83</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Alcohol and youth</topic><topic>Alcohol use</topic><topic>Analysis</topic><topic>Child</topic><topic>Child development</topic><topic>Drinking of alcoholic beverages</topic><topic>Electroencephalography</topic><topic>Ethanol</topic><topic>Female</topic><topic>Humans</topic><topic>Male</topic><topic>Marijuana</topic><topic>Polysomnography</topic><topic>REM sleep</topic><topic>Sleep</topic><topic>Sleep - physiology</topic><topic>Sleep Across the Lifespan</topic><topic>Sleep, REM - physiology</topic><topic>Sleep, Slow-Wave</topic><topic>Teenagers</topic><topic>Young Adult</topic><topic>Youth</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Kiss, Orsolya</creatorcontrib><creatorcontrib>Goldstone, Aimée</creatorcontrib><creatorcontrib>de Zambotti, Massimiliano</creatorcontrib><creatorcontrib>Yüksel, Dilara</creatorcontrib><creatorcontrib>Hasler, Brant P</creatorcontrib><creatorcontrib>Franzen, Peter L</creatorcontrib><creatorcontrib>Brown, Sandra A</creatorcontrib><creatorcontrib>De Bellis, Michael D</creatorcontrib><creatorcontrib>Nagel, Bonnie J</creatorcontrib><creatorcontrib>Nooner, Kate B</creatorcontrib><creatorcontrib>Tapert, Susan F</creatorcontrib><creatorcontrib>Colrain, Ian M</creatorcontrib><creatorcontrib>Clark, Duncan B</creatorcontrib><creatorcontrib>Baker, Fiona C</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>Health & Medical Collection</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 Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central Korea</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>Medical Database</collection><collection>Psychology Database</collection><collection>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 Central China</collection><collection>ProQuest One Psychology</collection><collection>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Sleep (New York, N.Y.)</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Kiss, Orsolya</au><au>Goldstone, Aimée</au><au>de Zambotti, Massimiliano</au><au>Yüksel, Dilara</au><au>Hasler, Brant P</au><au>Franzen, Peter L</au><au>Brown, Sandra A</au><au>De Bellis, Michael D</au><au>Nagel, Bonnie J</au><au>Nooner, Kate B</au><au>Tapert, Susan F</au><au>Colrain, Ian M</au><au>Clark, Duncan B</au><au>Baker, Fiona C</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Effects of emerging alcohol use on developmental trajectories of functional sleep measures in adolescents</atitle><jtitle>Sleep (New York, N.Y.)</jtitle><addtitle>Sleep</addtitle><date>2023-09-08</date><risdate>2023</risdate><volume>46</volume><issue>9</issue><spage>1</spage><pages>1-</pages><issn>0161-8105</issn><eissn>1550-9109</eissn><abstract>Abstract
Study Objectives
Adolescence is characterized by significant brain development, accompanied by changes in sleep timing and architecture. It also is a period of profound psychosocial changes, including the initiation of alcohol use; however, it is unknown how alcohol use affects sleep architecture in the context of adolescent development. We tracked developmental changes in polysomnographic (PSG) and electroencephalographic (EEG) sleep measures and their relationship with emergent alcohol use in adolescents considering confounding effects (e.g. cannabis use).
Methods
Adolescents (n = 94, 43% female, age: 12–21 years) in the National Consortium on Alcohol and Neurodevelopment in Adolescence (NCANDA) study had annual laboratory PSG recordings across 4-years. Participants were no/low drinkers at baseline.
Results
Linear mixed effect models showed developmental changes in sleep macrostructure and EEG, including a decrease in slow wave sleep and slow wave (delta) EEG activity with advancing age. Emergent moderate/heavy alcohol use across three follow-up years was associated with a decline in percentage rapid eye movement (REM) sleep over time, a longer sleep onset latency (SOL) and shorter total sleep time (TST) in older adolescents, and lower non-REM delta and theta power in males.
Conclusions
These longitudinal data show substantial developmental changes in sleep architecture. Emergent alcohol use during this period was associated with altered sleep continuity, architecture, and EEG measures, with some effects dependent on age and sex. These effects, in part, could be attributed to the effects of alcohol on underlying brain maturation processes involved in sleep–wake regulation.
Graphical Abstract</abstract><cop>US</cop><pub>Oxford University Press</pub><pmid>37058610</pmid><doi>10.1093/sleep/zsad113</doi><orcidid>https://orcid.org/0000-0002-3123-1106</orcidid><orcidid>https://orcid.org/0000-0001-9602-6165</orcidid><orcidid>https://orcid.org/0000-0003-2643-773X</orcidid><orcidid>https://orcid.org/0000-0002-0057-5977</orcidid><oa>free_for_read</oa></addata></record> |
| fulltext | fulltext |
| identifier | ISSN: 0161-8105 |
| ispartof | Sleep (New York, N.Y.), 2023-09, Vol.46 (9), p.1 |
| issn | 0161-8105 1550-9109 |
| language | eng |
| recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_10848227 |
| source | MEDLINE; Oxford University Press Journals All Titles (1996-Current); EZB-FREE-00999 freely available EZB journals; Alma/SFX Local Collection |
| subjects | Adolescent Adult Alcohol and youth Alcohol use Analysis Child Child development Drinking of alcoholic beverages Electroencephalography Ethanol Female Humans Male Marijuana Polysomnography REM sleep Sleep Sleep - physiology Sleep Across the Lifespan Sleep, REM - physiology Sleep, Slow-Wave Teenagers Young Adult Youth |
| title | Effects of emerging alcohol use on developmental trajectories of functional sleep measures in adolescents |
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