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Melatonin: From Pharmacokinetics to Clinical Use in Autism Spectrum Disorder
The role of melatonin has been extensively investigated in pathophysiological conditions, including autism spectrum disorder (ASD). Reduced melatonin secretion has been reported in ASD and led to many clinical trials using immediate-release and prolonged-release oral formulations of melatonin. Howev...
Autores principales: | , , , , , , , , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
MDPI
2021
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867370/ https://www.ncbi.nlm.nih.gov/pubmed/33540815 http://dx.doi.org/10.3390/ijms22031490 |
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author | Lalanne, Sébastien Fougerou-Leurent, Claire Anderson, George M. Schroder, Carmen M. Nir, Tali Chokron, Sylvie Delorme, Richard Claustrat, Bruno Bellissant, Eric Kermarrec, Solenn Franco, Patricia Denis, Laure Tordjman, Sylvie |
author_facet | Lalanne, Sébastien Fougerou-Leurent, Claire Anderson, George M. Schroder, Carmen M. Nir, Tali Chokron, Sylvie Delorme, Richard Claustrat, Bruno Bellissant, Eric Kermarrec, Solenn Franco, Patricia Denis, Laure Tordjman, Sylvie |
author_sort | Lalanne, Sébastien |
collection | PubMed |
description | The role of melatonin has been extensively investigated in pathophysiological conditions, including autism spectrum disorder (ASD). Reduced melatonin secretion has been reported in ASD and led to many clinical trials using immediate-release and prolonged-release oral formulations of melatonin. However, melatonin’s effects in ASD and the choice of formulation type require further study. Therapeutic benefits of melatonin on sleep disorders in ASD were observed, notably on sleep latency and sleep quality. Importantly, melatonin may also have a role in improving autistic behavioral impairments. The objective of this article is to review factors influencing treatment response and possible side effects following melatonin administration. It appears that the effects of exposure to exogenous melatonin are dependent on age, sex, route and time of administration, formulation type, dose, and association with several substances (such as tobacco or contraceptive pills). In addition, no major melatonin-related adverse effect was described in typical development and ASD. In conclusion, melatonin represents currently a well-validated and tolerated treatment for sleep disorders in children and adolescents with ASD. A more thorough consideration of factors influencing melatonin pharmacokinetics could illuminate the best use of melatonin in this population. Future studies are required in ASD to explore further dose-effect relationships of melatonin on sleep problems and autistic behavioral impairments. |
format | Online Article Text |
id | pubmed-7867370 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2021 |
publisher | MDPI |
record_format | MEDLINE/PubMed |
spelling | pubmed-78673702021-02-07 Melatonin: From Pharmacokinetics to Clinical Use in Autism Spectrum Disorder Lalanne, Sébastien Fougerou-Leurent, Claire Anderson, George M. Schroder, Carmen M. Nir, Tali Chokron, Sylvie Delorme, Richard Claustrat, Bruno Bellissant, Eric Kermarrec, Solenn Franco, Patricia Denis, Laure Tordjman, Sylvie Int J Mol Sci Review The role of melatonin has been extensively investigated in pathophysiological conditions, including autism spectrum disorder (ASD). Reduced melatonin secretion has been reported in ASD and led to many clinical trials using immediate-release and prolonged-release oral formulations of melatonin. However, melatonin’s effects in ASD and the choice of formulation type require further study. Therapeutic benefits of melatonin on sleep disorders in ASD were observed, notably on sleep latency and sleep quality. Importantly, melatonin may also have a role in improving autistic behavioral impairments. The objective of this article is to review factors influencing treatment response and possible side effects following melatonin administration. It appears that the effects of exposure to exogenous melatonin are dependent on age, sex, route and time of administration, formulation type, dose, and association with several substances (such as tobacco or contraceptive pills). In addition, no major melatonin-related adverse effect was described in typical development and ASD. In conclusion, melatonin represents currently a well-validated and tolerated treatment for sleep disorders in children and adolescents with ASD. A more thorough consideration of factors influencing melatonin pharmacokinetics could illuminate the best use of melatonin in this population. Future studies are required in ASD to explore further dose-effect relationships of melatonin on sleep problems and autistic behavioral impairments. MDPI 2021-02-02 /pmc/articles/PMC7867370/ /pubmed/33540815 http://dx.doi.org/10.3390/ijms22031490 Text en © 2021 by the authors. Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (http://creativecommons.org/licenses/by/4.0/). |
spellingShingle | Review Lalanne, Sébastien Fougerou-Leurent, Claire Anderson, George M. Schroder, Carmen M. Nir, Tali Chokron, Sylvie Delorme, Richard Claustrat, Bruno Bellissant, Eric Kermarrec, Solenn Franco, Patricia Denis, Laure Tordjman, Sylvie Melatonin: From Pharmacokinetics to Clinical Use in Autism Spectrum Disorder |
title | Melatonin: From Pharmacokinetics to Clinical Use in Autism Spectrum Disorder |
title_full | Melatonin: From Pharmacokinetics to Clinical Use in Autism Spectrum Disorder |
title_fullStr | Melatonin: From Pharmacokinetics to Clinical Use in Autism Spectrum Disorder |
title_full_unstemmed | Melatonin: From Pharmacokinetics to Clinical Use in Autism Spectrum Disorder |
title_short | Melatonin: From Pharmacokinetics to Clinical Use in Autism Spectrum Disorder |
title_sort | melatonin: from pharmacokinetics to clinical use in autism spectrum disorder |
topic | Review |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC7867370/ https://www.ncbi.nlm.nih.gov/pubmed/33540815 http://dx.doi.org/10.3390/ijms22031490 |
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