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Interactions between nocturnal melatonin secretion, metabolism, and sleeping behavior in adolescents with obesity
BACKGROUND/OBJECTIVES: Sleeping behavior and individual prospensity in sleep timing during a 24 h period, known as chronotypes, are underestimated factors, which may favor the development of obesity and metabolic diseases. Furthermore, melatonin is known to play an important role in circadian rhythm...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
Nature Publishing Group UK
2022
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050511/ https://www.ncbi.nlm.nih.gov/pubmed/35140394 http://dx.doi.org/10.1038/s41366-022-01077-4 |
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author | Overberg, Johanna Kalveram, Laura Keller, Theresa Krude, Heiko Kühnen, Peter Wiegand, Susanna |
author_facet | Overberg, Johanna Kalveram, Laura Keller, Theresa Krude, Heiko Kühnen, Peter Wiegand, Susanna |
author_sort | Overberg, Johanna |
collection | PubMed |
description | BACKGROUND/OBJECTIVES: Sleeping behavior and individual prospensity in sleep timing during a 24 h period, known as chronotypes, are underestimated factors, which may favor the development of obesity and metabolic diseases. Furthermore, melatonin is known to play an important role in circadian rhythm, but was also suggested to directly influence metabolism and bodyweight regulation. Since disturbed and shifted sleep rhythms have been observed in adolescents with obesity, this study aimed to investigate potential interactions between melatonin secretion, chronobiology, and metabolism. In addition, the influence of artificial light especially emitted by electronic devices on these parameters was of further interest. SUBJECTS/METHODS: We performed a cross-sectional study including 149 adolescents (mean age 14.7 ± 2.1 years) with obesity. Metabolic blood parameters (e.g., cholesterol, triglycerides, uric acid, and insulin) were obtained from patients and correlated with nocturnal melatonin secretion. Melatonin secretion was determined by measuring 6-sulfatoxymelatonin (MT6s), the major metabolite of melatonin in the first-morning urine, and normalized to urinary creatinine levels to account for the urinary concentration. Chronobiologic parameters were further assessed using the Munich ChronoType Questionnaire. RESULTS: Subjects with insulin resistance (n = 101) showed significantly lower nocturnal melatonin levels compared to those with unimpaired insulin secretion (p = 0.006). Furthermore, triglyceride (p = 0.012) and elevated uric acid levels (p = 0.029) showed significant associations with melatonin secretion. Patients with late chronotype showed a higher incidence of insulin resistance (p = 0.018). Moreover, late chronotype and social jetlag were associated with the time and duration of media consumption. CONCLUSION: We identified an association of impaired energy metabolism and lower nocturnal melatonin secretion in addition to late chronotype and increased social jetlag (misalignment of biological and social clocks) in adolescents with obesity. This might point towards a crucial role of chronotype and melatonin secretion as risk factors for the development of pediatric and adolescent obesity. |
format | Online Article Text |
id | pubmed-9050511 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2022 |
publisher | Nature Publishing Group UK |
record_format | MEDLINE/PubMed |
spelling | pubmed-90505112022-04-30 Interactions between nocturnal melatonin secretion, metabolism, and sleeping behavior in adolescents with obesity Overberg, Johanna Kalveram, Laura Keller, Theresa Krude, Heiko Kühnen, Peter Wiegand, Susanna Int J Obes (Lond) Article BACKGROUND/OBJECTIVES: Sleeping behavior and individual prospensity in sleep timing during a 24 h period, known as chronotypes, are underestimated factors, which may favor the development of obesity and metabolic diseases. Furthermore, melatonin is known to play an important role in circadian rhythm, but was also suggested to directly influence metabolism and bodyweight regulation. Since disturbed and shifted sleep rhythms have been observed in adolescents with obesity, this study aimed to investigate potential interactions between melatonin secretion, chronobiology, and metabolism. In addition, the influence of artificial light especially emitted by electronic devices on these parameters was of further interest. SUBJECTS/METHODS: We performed a cross-sectional study including 149 adolescents (mean age 14.7 ± 2.1 years) with obesity. Metabolic blood parameters (e.g., cholesterol, triglycerides, uric acid, and insulin) were obtained from patients and correlated with nocturnal melatonin secretion. Melatonin secretion was determined by measuring 6-sulfatoxymelatonin (MT6s), the major metabolite of melatonin in the first-morning urine, and normalized to urinary creatinine levels to account for the urinary concentration. Chronobiologic parameters were further assessed using the Munich ChronoType Questionnaire. RESULTS: Subjects with insulin resistance (n = 101) showed significantly lower nocturnal melatonin levels compared to those with unimpaired insulin secretion (p = 0.006). Furthermore, triglyceride (p = 0.012) and elevated uric acid levels (p = 0.029) showed significant associations with melatonin secretion. Patients with late chronotype showed a higher incidence of insulin resistance (p = 0.018). Moreover, late chronotype and social jetlag were associated with the time and duration of media consumption. CONCLUSION: We identified an association of impaired energy metabolism and lower nocturnal melatonin secretion in addition to late chronotype and increased social jetlag (misalignment of biological and social clocks) in adolescents with obesity. This might point towards a crucial role of chronotype and melatonin secretion as risk factors for the development of pediatric and adolescent obesity. Nature Publishing Group UK 2022-02-09 2022 /pmc/articles/PMC9050511/ /pubmed/35140394 http://dx.doi.org/10.1038/s41366-022-01077-4 Text en © The Author(s) 2022 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 Overberg, Johanna Kalveram, Laura Keller, Theresa Krude, Heiko Kühnen, Peter Wiegand, Susanna Interactions between nocturnal melatonin secretion, metabolism, and sleeping behavior in adolescents with obesity |
title | Interactions between nocturnal melatonin secretion, metabolism, and sleeping behavior in adolescents with obesity |
title_full | Interactions between nocturnal melatonin secretion, metabolism, and sleeping behavior in adolescents with obesity |
title_fullStr | Interactions between nocturnal melatonin secretion, metabolism, and sleeping behavior in adolescents with obesity |
title_full_unstemmed | Interactions between nocturnal melatonin secretion, metabolism, and sleeping behavior in adolescents with obesity |
title_short | Interactions between nocturnal melatonin secretion, metabolism, and sleeping behavior in adolescents with obesity |
title_sort | interactions between nocturnal melatonin secretion, metabolism, and sleeping behavior in adolescents with obesity |
topic | Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC9050511/ https://www.ncbi.nlm.nih.gov/pubmed/35140394 http://dx.doi.org/10.1038/s41366-022-01077-4 |
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