Melatonin is a neurohormone produced from serotonin which promotes sleep. The alterations in central and peripheral serotonin neurobiology and in circadian sleep-wake rhythms observed in autistic disorder suggest abnormalities in melatonin secretion. Several studies have reported a decrease in melatonin secretion in individuals with autism. Furthermore, nocturnal excretion of 6-Sulphatoxymelatonin (the predominant melatonin metabolite) was significantly negatively correlated with severity of autistic impairments in verbal communication and play. Melatonin could therefore have a therapeutic effect on sleep problems and may play a role in the pathophysiology of autistic disorder. These data highlight the possible therapeutic interest of an oral administration of melatonin in patients with autistic disorder. Thus, the objective of this clinical trial is to study the relation between the melatonin dose administered and its effect on severity of autistic impairments especially in verbal communication and play.
The hormone melatonin is of interest in autism due to theoretical considerations and reports of altered melatonin production in individuals with autism. Melatonin produced in the pineal gland helps regulate human circadian rhythms including sleep-wake, and is considered as the best measure of circadian rhythms. Several studies revealed that plasmatic and urinary nocturnal levels of melatonin are significantly lower in individuals with autism (in particular, in prepubertal children) compared to typically developing individuals. In addition, this reduction in nocturnal melatonin was significantly associated with the severity of communication and social interaction impairments, especially in verbal communication and play. Finally, diurnal excretion of melatonin was also found to be decreased in individuals with autistic disorder. Given these results, administration of melatonin could serve, at least in prepubertal children wih autism, to normalize physiological, developmental and behavioral processes that are influenced by this pineal hormone. A randomized clinical trial is therefore necessary to establish potential therapeutic efficacy of melatonin in autistic disorder and to specify its dose-effect relation. This is the first clinical trial studying the melatonin dose-effect in autism.
Study Type
INTERVENTIONAL
Allocation
RANDOMIZED
Purpose
TREATMENT
Masking
QUADRUPLE
Enrollment
34
Service de Psychiatrie de l'Enfant et de l'Adolescent - Hôpital de la Pitié-Salpêtrière
Paris, France
Centre Hospitalier Spécialisé Henri Laborit
Poitiers, France
Service de Psychothérapie de l'Enfant et de l'Adolescent - Hôpital Robert Debré
Reims, France
Pôle de Psychiatrie de l'Enfant et de l'Adolescent - Centre Hospitalier Guillaume Régnier
Rennes, France
Severity of autistic disorder
Time frame: 6 weeks after the beginning of the treatment.
Severity of autistic impairments
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ADOS (Autism Diagnostic Observation Scale)
Time frame: 3 weeks after the beginning of the treatment
Sleep problems
Sleep problems will be assessed using a parental questionnaire and an actimetry sensor in the child recording
Time frame: 3 weeks after the beginning of the treatment
Excretion of the urinary metabolite of melatonin
Diurnal and nocturnal excretion of the urinary metabolite of melatonin (6-Sulphatoxymelatonin)
Time frame: 3 weeks after the beginning of the treatment
Severity of autistic impairments
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ICG scale
Time frame: 3 weeks after the beginning of the treatment
Severity of autistic impairments
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ADOS (Autism Diagnostic Observation Scale)
Time frame: 6 weeks after the beginning of the treatment
Sleep problems
Sleep problems will be assessed using a parental questionnaire and an actimetry sensor in the child recording
Time frame: 6 weeks after the beginning of the treatment
Excretion of the urinary metabolite of melatonin
Diurnal and nocturnal excretion of the urinary metabolite of melatonin (6-Sulphatoxymelatonin)
Time frame: 6 weeks after the beginning of the treatment
Severity of autistic impairments
Severity of autistic impairments (global severity of autistic disorder and anxiety) using the ICG scale
Time frame: 6 weeks after the beginning of the treatment
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