Title of article :
Acute effects of mirtazapine on sleep continuity and sleep architecture in depressed patients: a pilot study
Author/Authors :
Andrew Winokur، نويسنده , , Michael J. Sateia، نويسنده , , J. Boyd Hayes، نويسنده , , Wendy Bayles-Dazet، نويسنده , , Mary M. MacDonald، نويسنده , , Keith A. Gary، نويسنده ,
Issue Information :
روزنامه با شماره پیاپی سال 2000
Pages :
4
From page :
75
To page :
78
Abstract :
Background: Mirtazapine, a clinically effective antidepressant, acts by antagonizing central α2-adrenergic and 5-HT2/5-HT3 receptors. No data are available regarding mirtazapine’s effects on sleep architecture in patients with major depressive disorder. Methods: Six patients meeting criteria for major depressive disorder and scoring ≥4 on the three Hamilton Depression Rating Scale sleep items were studied. Polysomnographic evaluations were performed at baseline and after 1 (15 mg at bedtime) and 2 weeks (30 mg at bedtime) of open-label mirtazapine treatment. Results: Mirtazapine significantly decreased sleep latency and significantly increased total sleep time and sleep efficiency from baseline levels during week 1, with similar results observed after week 2. Mirtazapine did not significantly alter rapid eye movement sleep parameters. Clinically, Hamilton Depression Rating Scale and sleep disturbance ratings improved after treatment. Conclusions: Mirtazapine significantly improves sleep continuity in major depressive disorder patients with poor sleep quality at weeks 1 and 2 of treatment, while preserving sleep architecture. Background: Mirtazapine, a clinically effective antidepressant, acts by antagonizing central α2-adrenergic and 5-HT2/5-HT3 receptors. No data are available regarding mirtazapine’s effects on sleep architecture in patients with major depressive disorder. Methods: Six patients meeting criteria for major depressive disorder and scoring ≥4 on the three Hamilton Depression Rating Scale sleep items were studied. Polysomnographic evaluations were performed at baseline and after 1 (15 mg at bedtime) and 2 weeks (30 mg at bedtime) of open-label mirtazapine treatment. Results: Mirtazapine significantly decreased sleep latency and significantly increased total sleep time and sleep efficiency from baseline levels during week 1, with similar results observed after week 2. Mirtazapine did not significantly alter rapid eye movement sleep parameters. Clinically, Hamilton Depression Rating Scale and sleep disturbance ratings improved after treatment. Conclusions: Mirtazapine significantly improves sleep continuity in major depressive disorder patients with poor sleep quality at weeks 1 and 2 of treatment, while preserving sleep architecture.
Keywords :
Polysomnography , depression , insomnia
Journal title :
Biological Psychiatry
Serial Year :
2000
Journal title :
Biological Psychiatry
Record number :
501251
Link To Document :
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