Gm. Saletu-zyhlarz et al., Nonorganic insomnia in panic disorder: Comparative sleep laboratory studies with normal controls and placebo-controlled trials with alprazolam, HUM PSYCHOP, 15(4), 2000, pp. 241-254
Citations number
89
Categorie Soggetti
Neurosciences & Behavoir
Journal title
HUMAN PSYCHOPHARMACOLOGY-CLINICAL AND EXPERIMENTAL
Objective and subjective sleep and awakening quality was investigated in 11
drug-free patients (4 females, 7 males) aged 30-55 (mean: 44+/-9) years wi
th nonorganic insomnia (F 51.0) related to panic disorder (F 41.0) as compa
red with 11 age- and sex-matched normal controls aged 30-58 (mean: 44+/-9)
years, utilising polysomnography (PSG) and psychometry. PSG demonstrated de
creased sleep efficiency (primary target variable), total sleep time (TST)
and S2 as well as increased middle and late insomnia, SI, S3 + S4, snoring
and PLM in patients. There were no intergroup differences in REM variables.
Subjective sleep quality deteriorated, as did drive and fine motor activit
y in the morning, while concentration increased. Blood pressure in the even
ing and morning and pulse rate in the evening were elevated. These differen
ces as compared with normals were distinct from those observed in other sle
ep disorders. In a subsequent acute, placebo-controlled cross-over design s
tudy, patients received alprazolam 0.5 mg (Xanor*) and placebo. As compared
with placebo, alprazolam induced an increase in sleep efficiency (primary
target variable), TST and S2, a decrease in wakefulness during the total sl
eep period, S3 + S4 and the oxygen desaturation and PLM indices, and improv
ed subjective sleep quality, somatic complaints, drive, affectivity and dro
wsiness in the morning. There were no changes in REM variables. Thus, alpra
zolam induced changes that were opposite to the differences observed betwee
n patients and controls before treatment, thereby normalizing sleep and awa
kening quality. As observed in insomnia related to GAD and subsequent benzo
diazepine therapy, the present study also points to a key-lock principle in
the treatment of insomnia caused by anxiety disorders and neurophysiologic
ally visualizes processes at the receptor level (e.g. benzodiazepine agonis
ts versus inverse agonists). Copyright (C) 2000 John Wiley & Sons, Ltd.