Effects of Tryptophan Depletion on Drug-Free Patients With Seasonal Affective Disorder During a Stable Response to Bright Light Therapy

1997 ◽  
Vol 54 (2) ◽  
pp. 133 ◽  
Author(s):  
Alexander Neumeister
2003 ◽  
Vol 13 ◽  
pp. S247-S248
Author(s):  
E. Pjrek ◽  
D. Winkler ◽  
A. Konstantinidis ◽  
N. Thierry ◽  
A. Heiden ◽  
...  

2000 ◽  
Vol 30 (1) ◽  
pp. 79-87 ◽  
Author(s):  
R. W. LAM ◽  
T. A. BOWERING ◽  
E. M. TAM ◽  
A. GREWAL ◽  
L. N. YATHAM ◽  
...  

Background. Serotonergic mechanisms have been proposed for the pathophysiology of seasonal affective disorder (SAD) and the therapeutic effect of bright-light treatment. Previously, we showed that SAD patients, in clinical remission with light therapy during the winter, experienced transient depressive relapses after a rapid tryptophan depletion (RTD) technique, which results in decreased brain serotonin levels. The objective of this study was to investigate the effect of RTD in SAD patients who were in natural summer remission.Methods. Twelve drug-free patients with SAD by DSM-IV criteria and 10 normal subjects participated in this double-blind, placebo-controlled, crossover study. SAD patients were in natural summer remission for at least 8 weeks. Behavioural ratings and plasma tryptophan levels were obtained before, and 5 h after, ingesting an amino acid (AA) mixture±tryptophan. Experimental RTD and control sessions were scheduled 1 week apart.Results. The RTD session resulted in significant reduction in total and free plasma tryptophan levels compared to the control session. The behavioural data were analysed using repeated measures analysis of variance. This analysis found significant main effects of time (higher scores after AA ingestion) and diagnosis (higher scores in SAD patients), but no main effect of session or significant interaction effects between the three factors. Thus, there were no significant behavioural effects of RTD compared to the sham depletion control session.Conclusions. The summer remission experienced by SAD patients is not dependent on plasma tryptophan levels (and presumably brain serotonin function) in the same manner as that of remission after light therapy. These results conflict with those of other laboratories, perhaps because of differences in study samples.


1995 ◽  
Vol 119 (2) ◽  
pp. 202-210 ◽  
Author(s):  
PAMELA F. GALLIN ◽  
MICHAEL TERMAN ◽  
CHARLOTTE E. REMÉ ◽  
BRIAN RAFFERTY ◽  
JIUAN SU TERMAN ◽  
...  

2018 ◽  
Vol 8 (1) ◽  
Author(s):  
Marie Spies ◽  
Gregory M. James ◽  
Chrysoula Vraka ◽  
Cécile Philippe ◽  
Marius Hienert ◽  
...  

2013 ◽  
Vol 202 (5) ◽  
pp. 352-356 ◽  
Author(s):  
Sallie Baxendale ◽  
John O'Sullivan ◽  
Dominic Heaney

BackgroundBright light therapy is an effective treatment for seasonal affective disorder and non-seasonal depression. Depression and anxiety are common psychiatric comorbidities in epilepsy.AimsTo examine the efficacy of bright light therapy for symptoms of anxiety and depression in adults with focal epilepsy (trial registration at ClinicalTrials.gov: NCT01028456).MethodWe recruited 101 adults with medically intractable focal epilepsy. Participants completed the Hospital Anxiety and Depression Scale (HADS) at the beginning (T1) and end of a 12-week baseline period (T2) and again after 12 weeks of daily light therapy (T3), with 51 participants using a high-intensity light box and 50 using a low-intensity one. Seizure diaries were kept throughout the baseline and trial period.ResultsA total of 58 patients completed the trial. Anxiety and depression scores were significantly reduced following the light therapy at T3in both the high- and low-intensity groups.ConclusionsLight therapy resulted in a significant reduction in symptoms of anxiety and depression but we did not find any differences between high- v. low-intensity treatment This may, therefore, be an effective treatment for symptoms of low mood in epilepsy at lower intensities than those typically used to treat seasonal affective disorder. Further work is needed to investigate this possibility with an adequate placebo condition.


CNS Spectrums ◽  
2001 ◽  
Vol 6 (6) ◽  
pp. 487-501 ◽  
Author(s):  
Paul H. Desan ◽  
Dan A. Oren

AbstractSeasonal affective disorder (SAD) is a form of depression that starts in the fall and ends in the spring. This article reviews existing theories about the relationship between circadian rhythms and the disorder. Recent research indicates that as with pharmacologic antidepressants, at least 2–4 weeks are needed to demonstrate the effectiveness of bright-light therapy compared to placebo. The response to such treatment is strongest with precisely timed light exposure: treatment is optimal during the morning hours when the circadian systemt is susceptible to phase advance. Such clinical improvement is correlated with the magnitude of the phase shift induced. These observations suggest a model of circadian function in SAD and provide important guidelines for its treatment.


1990 ◽  
Vol 44 (1) ◽  
pp. 169-170
Author(s):  
Takuro Endo ◽  
Toshiharu Takahashi ◽  
Megumi Ide ◽  
Hiroshi Itoh ◽  
Mitsuo Sasaki ◽  
...  

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