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The chronobiology and neurobiology of winter seasonal affective disorder

This review summarizes research on the chronobiology and neurobiology of winter seasonal affective disorder (SAD), a recurrent subtype of depression characterized by a predictable onset in the fall/winter months and spontaneous remission in the spring/summer period. Chronobiological mechanisms relat...

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Autor principal: Levitan, Robert D.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Les Laboratoires Servier 2007
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202491/
https://www.ncbi.nlm.nih.gov/pubmed/17969868
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author Levitan, Robert D.
author_facet Levitan, Robert D.
author_sort Levitan, Robert D.
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description This review summarizes research on the chronobiology and neurobiology of winter seasonal affective disorder (SAD), a recurrent subtype of depression characterized by a predictable onset in the fall/winter months and spontaneous remission in the spring/summer period. Chronobiological mechanisms related to circadian rhythms, melatonin, and photoperiodism play a significant role in many cases of SAD, and treatment of SAD can be optimized by considering individual differences in key chronobiological markers. Converging evidence also points to a role for the major monoamine neurotransmitters serotonin, norepinephrine, and dopamine in one or more aspects of SAD. Ultimately, as with other psychiatric illnesses, SAD is best considered as a complex disorder resulting from the interaction of several vulnerability factors acting at different levels, the various genetic mechanisms that underlie them, and the physical environment. Models of SAD that emphasize its potential role in human evolution will also be discussed.
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spelling pubmed-32024912011-10-27 The chronobiology and neurobiology of winter seasonal affective disorder Levitan, Robert D. Dialogues Clin Neurosci Clinical Research This review summarizes research on the chronobiology and neurobiology of winter seasonal affective disorder (SAD), a recurrent subtype of depression characterized by a predictable onset in the fall/winter months and spontaneous remission in the spring/summer period. Chronobiological mechanisms related to circadian rhythms, melatonin, and photoperiodism play a significant role in many cases of SAD, and treatment of SAD can be optimized by considering individual differences in key chronobiological markers. Converging evidence also points to a role for the major monoamine neurotransmitters serotonin, norepinephrine, and dopamine in one or more aspects of SAD. Ultimately, as with other psychiatric illnesses, SAD is best considered as a complex disorder resulting from the interaction of several vulnerability factors acting at different levels, the various genetic mechanisms that underlie them, and the physical environment. Models of SAD that emphasize its potential role in human evolution will also be discussed. Les Laboratoires Servier 2007-09 /pmc/articles/PMC3202491/ /pubmed/17969868 Text en Copyright: © 2007 LLS http://creativecommons.org/licenses/by-nc-nd/3.0/ This is an open-access article distributed under the terms of the Creative Commons Attribution License (http://creativecommons.org/licenses/by-nc-nd/3.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research
Levitan, Robert D.
The chronobiology and neurobiology of winter seasonal affective disorder
title The chronobiology and neurobiology of winter seasonal affective disorder
title_full The chronobiology and neurobiology of winter seasonal affective disorder
title_fullStr The chronobiology and neurobiology of winter seasonal affective disorder
title_full_unstemmed The chronobiology and neurobiology of winter seasonal affective disorder
title_short The chronobiology and neurobiology of winter seasonal affective disorder
title_sort chronobiology and neurobiology of winter seasonal affective disorder
topic Clinical Research
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3202491/
https://www.ncbi.nlm.nih.gov/pubmed/17969868
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