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Sleep dysfunction in Rett syndrome: a trial of exogenous melatonin treatment
Author(s) -
McArthur Angela J,
Budden Sarojini S
Publication year - 1998
Publication title -
developmental medicine and child neurology
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 1.658
H-Index - 143
eISSN - 1469-8749
pISSN - 0012-1622
DOI - 10.1111/j.1469-8749.1998.tb15445.x
Subject(s) - rett syndrome , melatonin , sleep (system call) , medicine , psychiatry , psychology , pediatrics , biology , computer science , biochemistry , gene , operating system
Nine girls with Rett syndrome (mean age, 10.1 years) were monitored 24 hours a day over a period of 10 weeks using wrist actigraphy. Baseline sleep‐wake patterns were assessed for 1 week. Subsequently, patients underwent a 4‐week melatonin treatment period in a double‐blind, placebo‐controlled, crossover protocol that employed a 1‐week washout between treatment trials. Melatonin doses ranged from 2.5 to 7.5 mg, based upon individual body weight. Baseline sleep quality was poor compared with healthy children. At baseline the group demonstrated a low sleep efficiency (mean [±SE], 68.0±3.9%), long sleep‐onset latency (42.1±12.0 minutes), and a short and fragmented total sleep time (7.5±0.3 hours; 15±2 awakenings per night). Melatonin significantly decreased sleep‐onset latency to (mean ± SE) 19.1±5.3 minutes (P<0.05) during the first 3 weeks of treatment. While the variability of individual responsiveness was high, melatonin appeared to improve total sleep time and sleep efficiency in the patients with the worse baseline sleep quality. Finally, a 4‐week administration of melatonin appears to be a safe treatment as no adverse side effects were detected, yet long‐term effects of chronic melatonin use in pediatric patients are unknown at this time.