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Gender differences in adolescent sleep neurophysiology: a high-density sleep EEG study
During adolescence, differences between males and females in physiology, behavior and risk for psychopathology are accentuated. The goal of the current study was to examine gender differences in sleep neurophysiology using high-density sleep EEG in early adolescence. We examined gender differences i...
Autores principales: | , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2020
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522718/ https://www.ncbi.nlm.nih.gov/pubmed/32985555 http://dx.doi.org/10.1038/s41598-020-72802-0 |
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author | Markovic, Andjela Kaess, Michael Tarokh, Leila |
author_facet | Markovic, Andjela Kaess, Michael Tarokh, Leila |
author_sort | Markovic, Andjela |
collection | PubMed |
description | During adolescence, differences between males and females in physiology, behavior and risk for psychopathology are accentuated. The goal of the current study was to examine gender differences in sleep neurophysiology using high-density sleep EEG in early adolescence. We examined gender differences in sleep EEG power and coherence across frequency bands for both NREM and REM sleep in a sample of 61 adolescents (31 girls and 30 boys; mean age = 12.48; SD = 1.34). In addition, sleep spindles were individually detected and characterized. Compared to boys, girls had significantly greater spindle activity, as reflected in higher NREM sigma power, spindle amplitude, spindle frequency and spindle density over widespread regions. Furthermore, power in higher frequency bands (16.2–44 Hz) was larger in girls than boys in a state independent manner. Oscillatory activity across frequency bands and sleep states was generally more coherent in females as compared to males, suggesting greater connectivity in females. An exception to this finding was the alpha band during NREM and REM sleep, where coherence was higher (NREM) or not different (REM) in boys compared to girls. Sleep spindles are generated through thalamocortical circuits, and thus, the greater spindle activity across regions in females may represent a stronger thalamocortical circuit in adolescent females as compared to males. Moreover, greater global connectivity in females may reflect functional brain differences with implications for cognition and mental health. Given the pronounced gender differences, our study highlights the importance of taking gender into account when designing and interpreting studies of sleep neurophysiology. |
format | Online Article Text |
id | pubmed-7522718 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2020 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-75227182020-09-29 Gender differences in adolescent sleep neurophysiology: a high-density sleep EEG study Markovic, Andjela Kaess, Michael Tarokh, Leila Sci Rep Article During adolescence, differences between males and females in physiology, behavior and risk for psychopathology are accentuated. The goal of the current study was to examine gender differences in sleep neurophysiology using high-density sleep EEG in early adolescence. We examined gender differences in sleep EEG power and coherence across frequency bands for both NREM and REM sleep in a sample of 61 adolescents (31 girls and 30 boys; mean age = 12.48; SD = 1.34). In addition, sleep spindles were individually detected and characterized. Compared to boys, girls had significantly greater spindle activity, as reflected in higher NREM sigma power, spindle amplitude, spindle frequency and spindle density over widespread regions. Furthermore, power in higher frequency bands (16.2–44 Hz) was larger in girls than boys in a state independent manner. Oscillatory activity across frequency bands and sleep states was generally more coherent in females as compared to males, suggesting greater connectivity in females. An exception to this finding was the alpha band during NREM and REM sleep, where coherence was higher (NREM) or not different (REM) in boys compared to girls. Sleep spindles are generated through thalamocortical circuits, and thus, the greater spindle activity across regions in females may represent a stronger thalamocortical circuit in adolescent females as compared to males. Moreover, greater global connectivity in females may reflect functional brain differences with implications for cognition and mental health. Given the pronounced gender differences, our study highlights the importance of taking gender into account when designing and interpreting studies of sleep neurophysiology. Nature Publishing Group UK 2020-09-28 /pmc/articles/PMC7522718/ /pubmed/32985555 http://dx.doi.org/10.1038/s41598-020-72802-0 Text en © The Author(s) 2020 Open Access This article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. |
spellingShingle | Article Markovic, Andjela Kaess, Michael Tarokh, Leila Gender differences in adolescent sleep neurophysiology: a high-density sleep EEG study |
title | Gender differences in adolescent sleep neurophysiology: a high-density sleep EEG study |
title_full | Gender differences in adolescent sleep neurophysiology: a high-density sleep EEG study |
title_fullStr | Gender differences in adolescent sleep neurophysiology: a high-density sleep EEG study |
title_full_unstemmed | Gender differences in adolescent sleep neurophysiology: a high-density sleep EEG study |
title_short | Gender differences in adolescent sleep neurophysiology: a high-density sleep EEG study |
title_sort | gender differences in adolescent sleep neurophysiology: a high-density sleep eeg study |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7522718/ https://www.ncbi.nlm.nih.gov/pubmed/32985555 http://dx.doi.org/10.1038/s41598-020-72802-0 |
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