Suvorexant alters dynamics of the sleep-electroencephalography-power spectrum and depressive-symptom trajectories during inpatient opioid withdrawal

Author:

Reid Matthew J1,Dunn Kelly E1,Abraham Liza1,Ellis Jennifer1ORCID,Hunt Carly2,Gamaldo Charlene E3,Coon William G45,Mun Chung Jung61,Strain Eric C1,Smith Michael T1,Finan Patrick H12ORCID,Huhn Andrew S1ORCID

Affiliation:

1. Department of Psychiatry and Behavioral Sciences, Johns Hopkins University School of Medicine , Baltimore, MD , USA

2. Department of Anesthesiology, University of Virginia School of Medicine , Charlottesville, VA , USA

3. Department of Neurology, Johns Hopkins University School of Medicine , Baltimore, MD , USA

4. Research and Exploratory Development Department, Johns Hopkins University Applied Physics Laboratory , Laurel, MD , USA

5. Johns Hopkins University Whiting School of Engineering , Baltimore, MD , USA

6. Arizona State University, Edson College of Nursing and Health Innovation , Pheonix, AZ , USA

Abstract

Abstract Study Objectives Opioid withdrawal is an aversive experience that often exacerbates depressive symptoms and poor sleep. The aims of the present study were to examine the effects of suvorexant on oscillatory sleep-electroencephalography (EEG) band power during medically managed opioid withdrawal, and to examine their association with withdrawal severity and depressive symptoms. Methods Participants with opioid use disorder (N = 38: age-range:21–63, 87% male, 45% white) underwent an 11-day buprenorphine taper, in which they were randomly assigned to suvorexant (20 mg [n = 14] or 40 mg [n = 12]), or placebo [n = 12], while ambulatory sleep-EEG data was collected. Linear mixed-effect models were used to explore: (1) main and interactive effects of drug group, and time on sleep-EEG band power, and (2) associations between sleep-EEG band power change, depressive symptoms, and withdrawal severity. Results Oscillatory spectral power tended to be greater in the suvorexant groups. Over the course of the study, decreases in delta power were observed in all study groups (β = −189.082, d = −0.522, p = <0.005), increases in beta power (20 mg: β = 2.579, d = 0.413, p = 0.009 | 40 mg β = 5.265, d = 0.847, p < 0.001) alpha power (20 mg: β = 158.304, d = 0.397, p = 0.009 | 40 mg: β = 250.212, d = 0.601, p = 0.001) and sigma power (20 mg: β = 48.97, d = 0.410, p < 0.001 | 40 mg: β = 71.54, d = 0.568, p < 0.001) were observed in the two suvorexant groups. During the four-night taper, decreases in delta power were associated with decreases in depressive symptoms (20 mg: β = 190.90, d = 0.308, p = 0.99 | 40 mg: β = 433.33, d = 0.889 p = <0.001), and withdrawal severity (20 mg: β = 215.55, d = 0.034, p = 0.006 | 40 mg: β = 192.64, d = −0.854, p = <0.001), in both suvorexant groups and increases in sigma power were associated with decreases in withdrawal severity (20 mg: β = −357.84, d = −0.659, p = 0.004 | 40 mg: β = −906.35, d = −1.053, p = <0.001). Post-taper decreases in delta (20 mg: β = 740.58, d = 0.964 p = <0.001 | 40 mg: β = 662.23, d = 0.882, p = <0.001) and sigma power (20 mg only: β = 335.54, d = 0.560, p = 0.023) were associated with reduced depressive symptoms in the placebo group. Conclusions Results highlight a complex and nuanced relationship between sleep-EEG power and symptoms of depression and withdrawal. Changes in delta power may represent a mechanism influencing depressive symptoms and withdrawal.

Funder

National Institute on Drug Abuse

Publisher

Oxford University Press (OUP)

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