Seasonal Affective Disorder: Neurobiology, Diagnosis, and Treatment

A special issue of Brain Sciences (ISSN 2076-3425).

Deadline for manuscript submissions: closed (25 January 2019) | Viewed by 4064

Special Issue Editor


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Guest Editor
Department of Psychological Medicine, Institute of Psychiatry, Psychology and Neurosciences-King’s College London, London SE5 8AF, UK
Interests: depression; bipolar; seasonal affective disorders; stress; HPA axis; psychoneuroendocrinology; antidepressants; mood stabilizers; epigenetic

Special Issue Information

Dear Colleagues,

Different seasons require unique strategies and clear behavioural, energetic, metabolic and immunological priorities. Recent research suggests a substantial role of seasonality in a variety of human conditions, such as cardiovascular disease, autoimmune disorders, anxiety, obsessive-compulsive disorder, major depression, mania, bipolar disorder and suicide rates.

Studies in seasonal affective disorder (SAD) found that manic episodes tend to peak in spring-summer and that depressive episodes peak at early winter, both as a form of recurrent depression, which usually occurs during winter and spontaneously resolves in spring/summer. Recent classification attempts to classify SAD as a separate disorder, seasonality is a specifier for both depressive and hypo/manic episodes. SAD is usually characterized by atypical symptoms, such as fatigue, hyperphagia, craving for carbohydrate-rich foods, along with weight gain, frequently preceding the functional impairments seen afterwards.

After light reaches photosensitive receptors in the eye, it sends a message through the Retino-Hypothalamic-Tract to the Suprachiasmatic Nucleus (SCN) of the hypothalamus. The SCN activates the Paraventricular nucleus of the hypothalamus (PVN), which liberates CRF and initiates HPA axis response. Serotonin and Norepinephrine neurons have vital connections with the SCN and the PVN, respectively. Serotonin is also a precursor of melatonin, and disturbances in tryptophan cascades may alter melatonin levels, disrupting even further the circadian rhythm, but a specific role for its dysfunction in SAD is still under discussion.

Because of its usual presentation with atypical symptoms, SAD has been described as a hypocortisolemic condition. However, there is no consensus evidence of the relation between SAD and HPA axis function.

SAD provides a unique window of opportunity to study physiological changes in affective disorders. The pharmacological treatment of SAD and the unusual feature that these patients tend to show improvements in mood after light treatment is a key topic in affective disorders.

Dr. Mario F. Juruena
Guest Editor

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Keywords

  • Seasonal Affective Disorders
  • Neuroendocrinology
  • Atypical Depression
  • Melatonin
  • Circadian Rhythm
  • Light Therapy
  • Retino-Hypothalamic-Tract
  • Serotonin
  • Norepinephrine
  • HPA axis

Published Papers (1 paper)

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Research

11 pages, 368 KiB  
Article
Effect of the Type and Number of Adverse Childhood Experiences and the Timing of Adverse Experiences on Clinical Outcomes in Individuals with Bipolar Disorder
by Young-Min Park, Tatyana Shekhtman and John R. Kelsoe
Brain Sci. 2020, 10(5), 254; https://doi.org/10.3390/brainsci10050254 - 27 Apr 2020
Cited by 12 | Viewed by 3576
Abstract
Studies have reported an association between adverse childhood experiences (ACEs) and the clinical outcomes of bipolar disorder (BD). However, these studies have several limitations; therefore, we aimed to clarify the effect of the type and number of ACEs and the timing of adverse [...] Read more.
Studies have reported an association between adverse childhood experiences (ACEs) and the clinical outcomes of bipolar disorder (BD). However, these studies have several limitations; therefore, we aimed to clarify the effect of the type and number of ACEs and the timing of adverse experiences on clinical outcomes in patients with BD. We analyzed the data of patients with BD (N = 2675) obtained from the National Institute of Mental Health: Bipolar Disorder Genetic Association Information Network, Translational Genomic Institute-I, and Translational Genomic Institute-II. All patients had been diagnosed using the Diagnostic Interview for Genetic Studies. ACEs were evaluated using the Childhood Life Events Scale (CLES). We analyzed the relationship between childhood trauma and clinical outcome in patients with and without exposure to ACEs. We found that ACEs had a robust negative effect on clinical outcomes, including earlier age at onset, presence of psychotic episodes, suicide attempts, mixed symptoms or episodes, substance misuse comorbidity, and worse life functioning. Specifically, the number of ACEs had the most significant effect on clinical outcomes; however, specific ACEs, such as physical abuse, had a considerable influence. Moreover, post-childhood adverse experiences had a weaker effect on clinical outcomes than ACEs did. There was an association of ACEs with negative clinical outcomes in patients with BD. This indicates the importance of basic and clinical research on ACEs in patients with BD. Full article
(This article belongs to the Special Issue Seasonal Affective Disorder: Neurobiology, Diagnosis, and Treatment)
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