The Use of Bright Light in the Treatment of Insomnia
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No Evidence for a Phase Delay in Human Circadian Rhythms After a Single Morning Melatonin Administration
J. Pineal Res. 2002; 32:1±5 Copyright ã Munksgaard, 2002 Journal of Pineal Research ISSN 0742-3098 No evidence for a phase delay in human circadian rhythms after a single morning melatonin administration Wirz-Justice A, Werth E, Renz C, MuÈ ller S, KraÈ uchi K. No evidence for a Anna Wirz-Justice, Esther Werth, phase delay in human circadian rhythms after a single morning melatonin Claudia Renz, Simon MuÈ ller and administration. J. Pineal Res. 2002; 32: 1±5. ã Munksgaard, 2002 Kurt KraÈuchi Abstract: Although there is good consensus that a single administration of Centre for Chronobiology, Psychiatric University Clinic, Basel, Switzerland melatonin in the early evening can phase advance human circadian rhythms, the evidence for phase delay shifts to a single melatonin stimulus given in the early morning is sparse. We therefore carried out a double-blind randomized- order placebo-controlled study under modi®ed constant routine (CR) conditions (58 hr bedrest under 8 lux with sleep 23:00±07:00 hr) in nine healthy young men. A single (pharmacological) dose of melatonin (5 mg p.o.) or a placebo was administered at 07:00 hr on the ®rst morning. Core body temperature (CBT) and heart rate (HR) were continuously recorded, and saliva was collected half-hourly for assay of melatonin. Neither the timing of the mid-range crossing times of temperature (MRCT) and HR rhythms, nor dim light melatonin onset (DLMOn) or oset (DLMO) were phase shifted the day after melatonin administration compared with placebo. Key words: human circadian rhythms, morning The only change was an altered wave form of the CBT rhythm: longer melatonin, phase delay duration of higher-than-average temperature after melatonin administration. -
The Effect of Bright Light on Affiliation
THE EFFECT OF ACUTE BRIGHT LIGHT EXPOSURE ON SOCIAL AFFILIATION By Copyright 2014 YEVGENY BOTANOV Submitted to the graduate degree program in Psychology and the Graduate Faculty of the University of Kansas in partial fulfillment of the requirements for the degree of Doctor of Philosophy. ________________________________________ Chairperson Stephen S. Ilardi, PhD ________________________________________ Monica Biernat, PhD ________________________________________ Rick E. Ingram, PhD ________________________________________ Sarah B. Kirk, PhD ________________________________________ Kyeung Hae Lee, PhD Date Defended: July 02, 2014 ii The Dissertation Committee for Yevgeny Botanov certifies that this is the approved version of the following dissertation: THE EFFECT OF ACUTE BRIGHT LIGHT EXPOSURE ON SOCIAL AFFILIATION ________________________________________ Chairperson Stephen S. Ilardi, PhD Date Approved: July 02, 2014 iii Abstract In recent decades, bright light has emerged as a useful tool in numerous clinical and non-clinical applications, with the potential to influence circadian rhythms, sleep, mood, and several other functional domains. However, despite the existence of plausible neurological pathways through which light could also influence social behavior, little is known at this point about the direct effects of bright light exposure on social interaction. Accordingly, the present study – utilizing a sample of young adults endorsing at least mild seasonal fluctuations in clinically relevant domains – examined the acute effects -
Seasonal Changes in Mood and Behavior Among Diverse
SEASONAL CHANGES IN MOOD AND BEHAVIOR AMONG CHILDREN AND ADOLESCENTS DISSERTATION Presented in Partial Fulfillment of the Requirements for the Degree Doctor of Philosophy in the Graduate School of The Ohio State University By Katharine Davies Smith, M.A. ***** The Ohio State University 2005 Dissertation Committee: Dr. Mary Fristad, Advisor Approved by Dr. Steven Beck ______________________ Dr. Michael Vasey Advisor Dr. Nancy Ryan-Wenger Department of Psychology Copyright by Katharine Davies Smith 2005 ABSTRACT Seasonal mood disorder (SMD) is likely prevalent among children and adolescents; however, there are few empirical investigations of pediatric SMD in the literature. To contribute to the field, the current study investigates the seasonality of mood and behavior among children and adolescents using longitudinal data collected from 1987 to 1998. One hundred eleven youths diagnosed with depression, 369 bereaved youths, 129 community controls, and their parents completed individual assessments at baseline, five, thirteen, and twenty-five months later. Assessment materials include several measures of depressive symptoms and diagnostic instruments. Multilevel analyses were conducted using MlwiN software. According to both parent- and child-report, youths from all three groups earn significantly higher total scores on measures of depression during the winter than the summer. On the other hand, significant seasonal effects do not arise for a measure of overall psychopathology. This implies that seasonality is limited to mood disorders. While this seasonal effect is significant, actual changes of mean scores on measures of depression from the summer to the winter are minimal, suggesting that season may have little affect on the mood and behavior for the majority of participants from each group. -
Bright Light Therapy for Bipolar Depression
Bright light therapy for bipolar depression Evidence suggests efficacy as an adjunctive treatment right light therapy (BLT) refers to the use of bright light to treat symptoms of depression. BLT was initially pre- scribed as a treatment for patients with seasonal affec- B 1 tive disorder. It was later found helpful for nonseasonal depression,2 premenstrual dysphoric disorder, postpartum depression, and phase shift circadian disorders, including for patients with dementia whose cognitive function improved after treatment with BLT.3 More recent studies suggest year- round benefit for nonseasonal depression.2 The American Psychiatric Association practice guidelines for the treatment of depression list BLT as an alternative and/or addition to pharmacologic and psychological treatment.4 BLT also may be beneficial for patients who are in the depressive phase of bipolar illness. This article describes the evidence, rationale for use, ANDRZEJ WOJCICKI mechanism of action, benefits, and safety profile of BLT for Suhayl J. Nasr, MD Ahmed Z. Elmaadawi, MD treating patients with bipolar depression. Professor of Psychiatry Adjunct Assistant Professor Indiana University School of Psychiatry of Medicine Indiana University School Indianapolis, Indiana of Medicine Circadian rhythm disruption in bipolar disorder Chief of Behavioral Indianapolis, Indiana Clinical manifestation. Patients with bipolar disorder (BD) Health Services Director of Interventional spend more time in depression than in mania.5 Sleep distur- Beacon Health System Psychiatry Division South Bend, Indiana Beacon Health System bance is a core symptom of BD; patients typically have little South Bend, Indiana need for sleep during a manic episode, and excess sleepiness Rikinkumar Patel, MD, during a depressive episode. -
Photobiomodulation and the Brain: a New Paradigm
HHS Public Access Author manuscript Author ManuscriptAuthor Manuscript Author J Opt. Author Manuscript Author manuscript; Manuscript Author available in PMC 2018 January 01. Published in final edited form as: J Opt. 2017 January ; 19(1): 013003–. doi:10.1088/2040-8986/19/1/013003. Photobiomodulation and the brain: a new paradigm Madison Hennessy1 and Michael R Hamblin2,3,4 1Briarcliff High School, Briarcliff Manor, NY, USA 2Wellman Center for Photomedicine, Massachusetts General Hospital, Boston, MA, USA 3Department of Dermatology, Harvard Medical School, Boston, MA, USA 4Harvard-MIT Division of Health Sciences and Technology, Cambridge, MA, USA Abstract Transcranial photobiomodulation (PBM) also known as low level laser therapy (tLLLT) relies on the use of red/NIR light to stimulate, preserve and regenerate cells and tissues. The mechanism of action involves photon absorption in the mitochondria (cytochrome c oxidase), and ion channels in cells leading to activation of signaling pathways, up-regulation of transcription factors, and increased expression of protective genes. We have studied PBM for treating traumatic brain injury (TBI) in mice using a NIR laser spot delivered to the head. Mice had improved memory and learning, increased neuroprogenitor cells in the dentate gyrus and subventricular zone, increased BDNF and more synaptogenesis in the cortex. These highly beneficial effects on the brain suggest that the applications of tLLLT are much broader than at first conceived. Other groups have studied stroke (animal models and clinical trials), Alzheimer’s disease, Parkinson’s disease, depression, and cognitive enhancement in healthy subjects. Keywords Transcranial photobiomodulation; low level laser therapy; brain disorders; traumatic brain injury; stroke; Alzheimer’s disease; psychiatric diseases 1 Introduction Light in the visible and near-infrared spectrum makes up the major part of solar radiation and is also provided by artificial light sources. -
Normal and Delayed Sleep Phases
1 Overview • Introduction • Circadian Rhythm Sleep Disorders – DSPS – Non-24 • Diagnosis • Treatment • Research Issues • Circadian Sleep Disorders Network © 2014 Circadian Sleep Disorders Network 2 Circadian Rhythms • 24 hours 10 minutes on average • Entrained to 24 hours (zeitgebers) • Suprachiasmatic nucleus (SCN) – the master clock • ipRGC cells (intrinsically photosensitive Retinal Ganglion Cells) © 2014 Circadian Sleep Disorders Network 3 Circadian Rhythm Sleep Disorders • Definition – A circadian rhythm sleep disorder is an abnormality of the body’s internal clock, in which a person is unable to fall asleep at a normal evening bedtime, although he is able to sleep reasonably well at other times dictated by his internal rhythm. • Complaints – Insomnia – Excessive daytime sleepiness • Inflexibility • Coordination with other circadian rhythms © 2014 Circadian Sleep Disorders Network 4 Circadian Sleep Disorder Subtypes* • Delayed Sleep-Phase Syndrome (G47.21**) • Non-24-Hour Sleep-Wake Disorder (G47.24) • Advanced Sleep-Phase Syndrome (G47.22) • Irregular Sleep-Wake Pattern (G47.23) • Shift Work Sleep Disorder (G47.26) • Jet Lag Syndrome * From The International Classification of Sleep Disorders, Revised (ICSD-R) ** ICD-10-CM diagnostic codes in parentheses © 2014 Circadian Sleep Disorders Network 5 Definition of DSPS from The International Classification of Sleep Disorders, Revised (ICSD-R): • Sleep-onset and wake times that are intractably later than desired • Actual sleep-onset times at nearly the same daily clock hour • Little or no reported difficulty in maintaining sleep once sleep has begun • Extreme difficulty awakening at the desired time in the morning, and • A relatively severe to absolute inability to advance the sleep phase to earlier hours by enforcing conventional sleep and wake times. -
Depression in Adults: Treatment and Management
Depression in adults: treatment and management Appendix J11: study characteristics for evidence from previous versions of the guideline (St John’s wort, seasonal affective disorder and relapse prevention) Depression in adults: Appendix J11 1 Contents Treatment of a new depressive episode ................................................................................................. 3 St John’s wort - studies in 2004 guideline ........................................................................................... 3 Seasonal affective disorder ................................................................................................................. 8 Light therapy - new studies in the guideline update ...................................................................... 8 Non-light therapy interventions for depression with a seasonal pattern/SAD ............................ 31 Relapse prevention ............................................................................................................................... 35 2004 Guideline .............................................................................................................................. 35 2009 Guideline .............................................................................................................................. 40 Seasonal affective disorder ............................................................................................................... 49 Non-light therapy interventions for depression with a seasonal pattern/SAD - -
Circadian Phase Sleep and Mood Disorders (PDF)
129 CIRCADIAN PHASE SLEEP AND MOOD DISORDERS ALFRED J. LEWY CIRCADIAN ANATOMY AND PHYSIOLOGY SCN Efferent Pathways Anatomy Not much is known about how the SCN entrains overt circadian rhythms. We know that the SCN is the master The Suprachiasmatic Nucleus: Locus of the pacemaker, but regarding its regulation of the rest/activity Biological Clock cycle, core body temperature rhythm and cortisol rhythm, Much is known about the neuroanatomic connections of among others, it is not clear if there is a humoral factor or the circadian system. In vertebrates, the locus of the biologi- neural connection that transmits the SCN’s efferent signal; cal clock (the endogenous circadian pacemaker, or ECP) however, a great deal is known about the efferent neural pathway between the SCN and pineal gland. that drives all circadian rhythms is in the hypothalamus, specifically, the suprachiasmatic nucleus (SCN)(1,2).This paired structure derives its name because it lies just above The Pineal Gland the optic chiasm. It contains about 10,000 neurons. The In mammals, the pineal gland is located in the center of molecular mechanisms of the SCN are an active area of the brain; however, it lies outside the blood–brain barrier. research. There is also a great deal of interest in clock genes Postganglionic sympathetic nerves (called the nervi conarii) and clock components of cells in general, not just in the from the superior cervical ganglion innervate the pineal (4). SCN. The journal Science designated clock genes as the The preganglionic neurons originate in the spinal cord, spe- second most important breakthrough for the recent year; cifically in the thoracic intermediolateral column. -
Non-24-Hour Sleep-Wake Disorder Revisited – a Case Study
CASE REPORT published: 29 February 2016 doi: 10.3389/fneur.2016.00017 Non-24-Hour Sleep-Wake Disorder Revisited – a Case study Corrado Garbazza1,2† , Vivien Bromundt3† , Anne Eckert2,4 , Daniel P. Brunner5 , Fides Meier2,4 , Sandra Hackethal6 and Christian Cajochen1,2* 1 Centre for Chronobiology, Psychiatric Hospital of the University of Basel, Basel, Switzerland, 2 Transfaculty Research Platform Molecular and Cognitive Neurosciences, University of Basel, Basel, Switzerland, 3 Sleep-Wake-Epilepsy-Centre, Department of Neurology, Inselspital, Bern University Hospital, Bern, Switzerland, 4 Neurobiology Laboratory for Brain Aging and Mental Health, Psychiatric Hospital of the University of Basel, Basel, Switzerland, 5 Center for Sleep Medicine, Hirslanden Clinic Zurich, Zurich, Switzerland, 6 Charité – Universitaetsmedizin Berlin, Berlin, Germany The human sleep-wake cycle is governed by two major factors: a homeostatic hourglass process (process S), which rises linearly during the day, and a circadian process C, which determines the timing of sleep in a ~24-h rhythm in accordance to the external Edited by: Ahmed S. BaHammam, light–dark (LD) cycle. While both individual processes are fairly well characterized, the King Saud University, Saudi Arabia exact nature of their interaction remains unclear. The circadian rhythm is generated by Reviewed by: the suprachiasmatic nucleus (“master clock”) of the anterior hypothalamus, through Axel Steiger, cell-autonomous feedback loops of DNA transcription and translation. While the phase Max Planck Institute of Psychiatry, Germany length (tau) of the cycle is relatively stable and genetically determined, the phase of Timo Partonen, the clock is reset by external stimuli (“zeitgebers”), the most important being the LD National Institute for Health and Welfare, Finland cycle. -
Light Therapy and Seasonal Affective Disorder (SAD)
Standard Research Article Psychother Psychosom 2020;89:17–24 Received: May 23, 2019 DOI: 10.1159/000502891 Accepted after revision: August 22, 2019 Published online: October 1, 2019 The Efficacy of Light Therapy in the Treatment of Seasonal Affective Disorder: A Meta-Analysis of Randomized Controlled Trials a a a, b a c Edda Pjrek Michaela-Elena Friedrich Luca Cambioli Markus Dold Fiona Jäger a a a a Arkadiusz Komorowski Rupert Lanzenberger Siegfried Kasper Dietmar Winkler a Department of Psychiatry and Psychotherapy, Medical University of Vienna, Vienna, Austria; b Competence Center for Eating Behavior, Obesity and the Psyche, Zofingen Hospital, Zofingen, Switzerland; c University Medical Center Freiburg, University of Freiburg, Freiburg, Germany Keywords moderate heterogeneity of the studies and a moderate-to- Seasonal affective disorder · Winter depression · high risk of bias. Conclusions: BLT can be regarded as an ef- Bright light therapy · Meta-analysis fective treatment for SAD, but the available evidence stems from methodologically heterogeneous studies with small- to-medium sample sizes, necessitating larger high-quality Abstract clinical trials. © 2019 S. Karger AG, Basel Background: Bright light therapy (BLT) has been used as a treatment for seasonal affective disorder (SAD) for over 30 years. This meta-analysis was aimed to assess the efficacy of BLT in the treatment of SAD in adults. Method: We per- Introduction formed a systematic literature search including randomized, single- or double-blind clinical trials investigating BLT Seasonal affective disorder (SAD) is a subtype of recur- ( 1,000 lx, light box or light visor) against dim light ( 400 lx) ≥ ≤ rent major depressive or bipolar disorder defined by a or sham/low-density negative ion generators as placebo. -
An Integrative Chronobiological-Cognitive Approach to Seasonal Affective Disorder Jennifer Nicole Rough University of Vermont
University of Vermont ScholarWorks @ UVM Graduate College Dissertations and Theses Dissertations and Theses 2016 An integrative chronobiological-cognitive approach to seasonal affective disorder Jennifer Nicole Rough University of Vermont Follow this and additional works at: https://scholarworks.uvm.edu/graddis Part of the Clinical Psychology Commons Recommended Citation Rough, Jennifer Nicole, "An integrative chronobiological-cognitive approach to seasonal affective disorder" (2016). Graduate College Dissertations and Theses. 483. https://scholarworks.uvm.edu/graddis/483 This Dissertation is brought to you for free and open access by the Dissertations and Theses at ScholarWorks @ UVM. It has been accepted for inclusion in Graduate College Dissertations and Theses by an authorized administrator of ScholarWorks @ UVM. For more information, please contact [email protected]. AN INTEGRATIVE CHRONOBIOLOGICAL-COGNITIVE APPROACH TO SEASONAL AFFECTIVE DISORDER A Dissertation Presented by Jennifer Nicole Rough to the Faculty of the Graduate College of the University of Vermont In Partial Fulfillment of the Requirements for the Degree of Doctor of Philosophy Specializing in Clinical Psychology January, 2016 Defense Date: September, 17, 2015 Dissertation Examination Committee: Kelly Rohan, Ph.D., Advisor Terry Rabinowitz, M.D., Chairperson Timothy Stickle, Ph.D. Mark Bouton, Ph.D. Donna Toufexis, Ph.D. Cynthia J. Forehand, Ph.D., Dean of the Graduate College ABSTRACT Seasonal affective disorder (SAD) is characterized by annual recurrence of clinical depression in the fall and winter months. The importance of SAD as a public health problem is underscored by its high prevalence (an estimated 5%) and by the large amount of time individuals with SAD are impaired (on average, 5 months each year). -
A Three Pulse Phase Response Curve to Three Milligrams of Melatonin in Humans
J Physiol 586.2 (2008) pp 639–647 639 A three pulse phase response curve to three milligrams of melatonin in humans Helen J. Burgess1,VictoriaL.Revell2 and Charmane I. Eastman1 1Biological Rhythms Research Laboratory, Department of Behavioural Sciences, Rush University Medical Center, Chicago, IL, USA 2Faculty of Health and Medical Sciences, University of Surrey, Guildford, Surrey GU2 7XH, UK Exogenousmelatoninisincreasinglyusedforitsphaseshiftingandsoporificeffects.Wegenerated a three pulse phase response curve (PRC) to exogenous melatonin (3 mg) by administering it to free-running subjects. Young healthy subjects (n = 27) participated in two 5 day laboratory sessions,eachprecededbyatleastaweekofhabitual,butfixedsleep.Each5 daylaboratorysession started and ended with a phase assessment to measure the circadian rhythm of endogenous melatonin in dim light using 30 min saliva samples. In between were three days in an ultradian dim light (< 150 lux)–dark cycle (LD 2.5 : 1.5) during which each subject took one pill per day at the same clock time (3 mg melatonin or placebo, double blind, counterbalanced). Each individual’s phase shift to exogenous melatonin was corrected by subtracting their phase shift to placebo (a free-run). The resulting PRC has a phase advance portion peaking about 5 h before the dim light melatonin onset, in the afternoon. The phase delay portion peaks about 11 h after the dim light melatonin onset, shortly after the usual time of morning awakening. A dead zone of minimal phase shifts occurred around the first half of habitual sleep. The fitted maximum advance and delay shifts were 1.8 h and 1.3 h, respectively. This new PRC will aid in determining the optimal time to administer exogenous melatonin to achieve desired phase shifts and demonstrates that using exogenous melatonin as a sleep aid at night has minimal phase shifting effects.