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Melanopic irradiance defines the impact of evening display light on sleep latency, melatonin and alertness
Evening light-emitting visual displays may disrupt sleep, suppress melatonin and increase alertness. Here, we control melanopic irradiance independent of display luminance and colour, in 72 healthy males 4 h before habitual bedtime and expose each of them to one of four luminance levels (i.e., dim l...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2023
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974389/ https://www.ncbi.nlm.nih.gov/pubmed/36854795 http://dx.doi.org/10.1038/s42003-023-04598-4 |
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author | Schöllhorn, Isabel Stefani, Oliver Lucas, Robert J. Spitschan, Manuel Slawik, Helen C. Cajochen, Christian |
author_facet | Schöllhorn, Isabel Stefani, Oliver Lucas, Robert J. Spitschan, Manuel Slawik, Helen C. Cajochen, Christian |
author_sort | Schöllhorn, Isabel |
collection | PubMed |
description | Evening light-emitting visual displays may disrupt sleep, suppress melatonin and increase alertness. Here, we control melanopic irradiance independent of display luminance and colour, in 72 healthy males 4 h before habitual bedtime and expose each of them to one of four luminance levels (i.e., dim light, smartphone, tablet or computer screen illuminance) at a low and a high melanopic irradiance setting. Low melanopic light shortens the time to fall asleep, attenuates evening melatonin suppression, reduces morning melatonin, advances evening melatonin onset and decreases alertness compared to high melanopic light. In addition, we observe dose-dependent increases in sleep latency, reductions in melatonin concentration and delays in melatonin onset as a function of melanopic irradiance—not so for subjective alertness. We identify melanopic irradiance as an appropriate parameter to mitigate the unwanted effects of screen use at night. Our results may help the many people who sit in front of screens in the evening or at night to fall asleep faster, feel sleepier, and have a more stable melatonin phase by spectrally tuning the visual display light without compromising the visual appearance. |
format | Online Article Text |
id | pubmed-9974389 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2023 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-99743892023-03-01 Melanopic irradiance defines the impact of evening display light on sleep latency, melatonin and alertness Schöllhorn, Isabel Stefani, Oliver Lucas, Robert J. Spitschan, Manuel Slawik, Helen C. Cajochen, Christian Commun Biol Article Evening light-emitting visual displays may disrupt sleep, suppress melatonin and increase alertness. Here, we control melanopic irradiance independent of display luminance and colour, in 72 healthy males 4 h before habitual bedtime and expose each of them to one of four luminance levels (i.e., dim light, smartphone, tablet or computer screen illuminance) at a low and a high melanopic irradiance setting. Low melanopic light shortens the time to fall asleep, attenuates evening melatonin suppression, reduces morning melatonin, advances evening melatonin onset and decreases alertness compared to high melanopic light. In addition, we observe dose-dependent increases in sleep latency, reductions in melatonin concentration and delays in melatonin onset as a function of melanopic irradiance—not so for subjective alertness. We identify melanopic irradiance as an appropriate parameter to mitigate the unwanted effects of screen use at night. Our results may help the many people who sit in front of screens in the evening or at night to fall asleep faster, feel sleepier, and have a more stable melatonin phase by spectrally tuning the visual display light without compromising the visual appearance. Nature Publishing Group UK 2023-03-01 /pmc/articles/PMC9974389/ /pubmed/36854795 http://dx.doi.org/10.1038/s42003-023-04598-4 Text en © The Author(s) 2023 https://creativecommons.org/licenses/by/4.0/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 license, and indicate if changes were made. The images or other third party material in this article are included in the article’s Creative Commons license, unless indicated otherwise in a credit line to the material. If material is not included in the article’s Creative Commons license 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 license, visit http://creativecommons.org/licenses/by/4.0/ (https://creativecommons.org/licenses/by/4.0/) . |
spellingShingle | Article Schöllhorn, Isabel Stefani, Oliver Lucas, Robert J. Spitschan, Manuel Slawik, Helen C. Cajochen, Christian Melanopic irradiance defines the impact of evening display light on sleep latency, melatonin and alertness |
title | Melanopic irradiance defines the impact of evening display light on sleep latency, melatonin and alertness |
title_full | Melanopic irradiance defines the impact of evening display light on sleep latency, melatonin and alertness |
title_fullStr | Melanopic irradiance defines the impact of evening display light on sleep latency, melatonin and alertness |
title_full_unstemmed | Melanopic irradiance defines the impact of evening display light on sleep latency, melatonin and alertness |
title_short | Melanopic irradiance defines the impact of evening display light on sleep latency, melatonin and alertness |
title_sort | melanopic irradiance defines the impact of evening display light on sleep latency, melatonin and alertness |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9974389/ https://www.ncbi.nlm.nih.gov/pubmed/36854795 http://dx.doi.org/10.1038/s42003-023-04598-4 |
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