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In major depressive disorder (MDD), main clinical features include insomnia and increased daytime sleepiness. However, specific treatment options to promote sleep in MDD are limited. Gamma-hydroxybutyrate (GHB, clinically administered as sodium oxybate) is a GHB/GABAB receptor agonist used clinically in narcolepsy, where it promotes restorative slow-wave sleep (SWS) while reducing next-day sleepiness. Therefore, we performed a randomized, placebo- and active comparator-controlled, double-blind, crossover trial to investigate the sleep-promoting properties of GHB in individuals with MDD. Outpatients aged 20-65 years fulfilling the DSM-V criteria for MDD were enrolled. A single dose of GHB (50mg/kg) was compared with a single dose of the clinical competitor trazodone (1.5 mg/kg) and placebo. Of 29 randomized patients, 23 received at least one intervention and were included in the analysis. Primary outcomes were slow wave sleep ([SWS], as % of total sleep time [TST]) assessed by polysomnography and next-day vigilance (median response time and number of lapses in the psychomotor vigilance test [PVT]). GHB robustly prolonged SWS compared to both trazodone and placebo. GHB also prolonged TST and enhanced sleep efficiency (TST % of time-in-bed), while reducing sleep stages N1, N2, and wake-after-sleep-onset. While the median response time on the PVT was unaffected, GHB reduced the number of lapses compared to trazodone and placebo. No serious adverse events occurred. A single nocturnal dose of GHB effectively promotes SWS and shows more favorable effects on next-day vigilance than trazodone and placebo. Future studies should investigate GHB in clinical settings, including repeated administration.
In major depressive disorder (MDD), main clinical features include insomnia and increased daytime sleepiness. However, specific treatment options to promote sleep in MDD are limited. Gamma-hydroxybutyrate (GHB, clinically administered as sodium oxybate) is a GHB/GABAB receptor agonist used clinically in narcolepsy, where it promotes restorative slow-wave sleep (SWS) while reducing next-day sleepiness. Therefore, we performed a randomized, placebo- and active comparator-controlled, double-blind, crossover trial to investigate the sleep-promoting properties of GHB in individuals with MDD. Outpatients aged 20-65 years fulfilling the DSM-V criteria for MDD were enrolled. A single dose of GHB (50mg/kg) was compared with a single dose of the clinical competitor trazodone (1.5 mg/kg) and placebo. Of 29 randomized patients, 23 received at least one intervention and were included in the analysis. Primary outcomes were slow wave sleep ([SWS], as % of total sleep time [TST]) assessed by polysomnography and next-day vigilance (median response time and number of lapses in the psychomotor vigilance test [PVT]). GHB robustly prolonged SWS compared to both trazodone and placebo. GHB also prolonged TST and enhanced sleep efficiency (TST % of time-in-bed), while reducing sleep stages N1, N2, and wake-after-sleep-onset. While the median response time on the PVT was unaffected, GHB reduced the number of lapses compared to trazodone and placebo. No serious adverse events occurred. A single nocturnal dose of GHB effectively promotes SWS and shows more favorable effects on next-day vigilance than trazodone and placebo. Future studies should investigate GHB in clinical settings, including repeated administration.
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