Aj. Mcarthur et Ss. Budden, SLEEP DYSFUNCTION IN RETT-SYNDROME - A TRIAL OF EXOGENOUS MELATONIN TREATMENT, Developmental Medicine and Child Neurology, 40(3), 1998, pp. 186-192
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, Baselin
e sleep-wake patterns were assessed for 1 week, Subsequently, patients
underwent a 4-week melatonin treatment period in a double-blind, plac
ebo-controlled, crossover protocol that employed a 1-week washout betw
een 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 decre
ased 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 indivi
dual responsiveness was high, melatonin appeared to improve total slee
p time and sleep efficiency in the patients with the worse baseline sl
eep 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 unkno
wn at this time.