Gj. Emslie et al., Sleep polysomnography as a predictor of recurrence in children and adolescents with major depressive disorder, IN J NEUROP, 4(2), 2001, pp. 159-168
Adults with major depressive disorder (MDD) demonstrate certain sleep polys
omnographic abnormalities, including sleep continuity disturbances, reduced
slow-wave sleep, shortened rapid eye movement (REM) latency, and increased
REM density. Findings of sleep EEG studies in depressed children and adole
scents have yielded conflicting results, possibly because of methodological
variations across the studies. Generally, however, studies have demonstrat
ed that depressed children and adolescents exhibit less sleep continuity an
d non-REM sleep differences in comparison with control subjects than do adu
lts. Thus, results from adult sleep polysomnography studies cannot necessar
ily be generalized to children and adolescents. Depressed adults who have r
educed REM latency during the symptomatic episode appear more likely to hav
e a relapse once treatment is discontinued than those with normal REM laten
cy. No studies of the relationship between sleep polysomnographic variables
and clinical course have been reported in depressed children and adolescen
ts. Data for baseline clinical variables and 3 nights of sleep polysomnogra
phy were examined in 113 depressed children (less than or equal to 12 yr: n
= 51) and adolescents (greater than or equal to 13 yr; n = 62) (56 in-pati
ents and 57 outpatients) where data was available on at least I yr of natur
alistic follow-up. Subjects came from 2 studies of sleep polysomnography in
children and adolescents with MDD. Clinical course was assessed using the
Kiddie-Longitudinal Interval Follow-Up Evaluation IK-LIFE). This interview
was used to define recovery from the index episode of MDD and recurrence, a
new episode of meeting hill criteria for MDD. Clinically within 1 yr of in
itial evaluation 102/113 subjects had recovered from their index episode of
depression (minimal or no symptoms for 60 d). Of the 102 subjects who reco
vered, 36 (35.3 %) had a recurrence of MDD. The majority of subjects (55 %)
who had a recurrence were not on medication at the time of recurrence. Sub
jects who had a recurrence were more likely to report suicidal thoughts or
attempts at baseline compared to those without a recurrence (67 vs. 37%; F
= 8.77; p = 0.004). On baseline sleep polysomnography, subjects with a late
r recurrence had decreased sleep efficiency and delayed sleep onset (sleep
latency > 10 min). Probability of recurrence at 12 months was 0.39 compared
to 0.15 in subjects with non-delayed sleep onset (p = 0.005). Baseline sui
cidal ideation and sleep dysregulation on sleep polysomnography predicted r
ecurrence in a large sample of depressed children and adolescents. Depressi
on in children and adolescents is frequently a chronic, recurrent illness.
Factors that can predict clinical course are important in increasing our un
derstanding of depression in this age group.