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A two-part, double-blind, placebo-controlled trial of exogenous melatonin in REM sleep behaviour disorder.

Journal of sleep research
December 1, 2010
Dieter Kunz et al. (2 authors)
Journal ArticleRandomized Controlled TrialHuman StudyClinical
Study Details

Study Goal

The researchers aimed to confirm whether exogenous melatonin improves REM sleep behaviour disorder (RBD) by reducing muscle atonia loss during REM sleep and improving clinical symptoms.

Results Summary

Melatonin significantly reduced the number of REM sleep epochs without muscle atonia (39% to 27%) and improved clinical global impression scores (6.1 to 4.6). Some benefits persisted even after switching to placebo, suggesting a potential carryover effect.

Population

Eight males (mean age 54 years) with polysomnographically confirmed RBD.

Effective Dosage

3 mg daily, administered between 22:00 h and 23:00 h.

Duration

4 weeks per treatment phase (placebo and melatonin) in a cross-over design.

Interactions

None mentioned

Extracted Claims (4)
InterventionDirectionEndpointPopulationDosageImpactClaim #
melatonin
decrease
number of 30-s REM sleep epochs without muscle atonia
patients with RBD
39% versus 27%
significantly reduced
#1
melatonin
increase
clinical global impression (CGI)
patients with RBD
6.1 versus 4.6
significant improvement
#2
placebo
decrease
number of REM sleep epochs without muscle atonia
patients who took placebo during Part II after having received melatonin in Part I
-16% compared to baseline
remained lower
#3
melatonin
increase
REM sleep muscle atonia
patients who took placebo during Part I
-
improvements
#4
Abstract

Rapid eye movement (REM) sleep behaviour disorder (RBD) has been suggested to predict the development of neurodegenerative disorders. Patients with RBD are acting out dream behaviour associated with loss of normal muscle atonia of REM sleep. The aim of the present study was to confirm that exogenous melatonin improves RBD. Eight consecutively recruited males (mean age 54 years) with a polysomnographically (PSG) confirmed diagnosis of RBD were included in a two-part, randomized, double-blind, placebo-controlled cross-over study. Patients received placebo and 3 mg of melatonin daily in a cross-over design, administered between 22:00 h and 23:00 h over a period of 4 weeks. PSG recordings were performed in all patients at baseline, at the end of Part I of the trial and at the end of Part II of the trial. Compared to baseline, melatonin significantly reduced the number of 30-s REM sleep epochs without muscle atonia (39% versus 27%; P = 0.012), and led to a significant improvement in clinical global impression (CGI: 6.1 versus 4.6; P = 0.024). Interestingly, the number of REM sleep epochs without muscle atonia remained lower in patients who took placebo during Part II after having received melatonin in Part I (-16% compared to baseline; P = 0.043). In contrast, patients who took placebo during Part I showed improvements in REM sleep muscle atonia only during Part II (i.e. during melatonin treatment). The data suggest that melatonin might be a second useful agent besides clonazepam in the treatment of RBD.

Medical Subject Headings (MeSH)
AdultAgedCentral Nervous System DepressantsDouble-Blind MethodHumansMaleMelatoninMiddle AgedPolysomnographyREM Sleep Behavior DisorderSleepSleep, REMTreatment Outcome
Study Links
Quality Scores
SafetyNot Assessed
Efficacy85/10
Quality80/10
Citation Metrics
Total Citations157
Citations/Year10.5
Relative Citation Ratio5.21
NIH Percentile93.5%
Research Impact Scores
APT Score0.95
Weight Score1.44
Normalized Score0.70
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