Hyperarousal features in the sleep architecture of individuals with and without insomnia

Author:

Di Marco Tobias12ORCID,Scammell Thomas E.3,Sadeghi Kolia4,Datta Alexandre N.5,Little David4,Tjiptarto Nurkurniati4,Djonlagic Ina3ORCID,Olivieri Antonio1,Zammit Gary6,Krystal Andrew7,Pathmanathan Jay4,Donoghue Jacob4,Hubbard Jeffrey1ORCID,Dauvilliers Yves8

Affiliation:

1. Idorsia Pharmaceuticals Ltd Allschwil Switzerland

2. Department of Clinical Research University of Basel Basel Switzerland

3. Department of Neurology Beth Israel Deaconess Medical Center Boston Massachusetts USA

4. Beacon Biosignals, Inc. Boston Massachusetts USA

5. University Children's Hospital Basel Basel Switzerland

6. Clinilabs Drug Development Corporation New York New York USA

7. University of California San Francisco California USA

8. Centre National de Référence Narcolepsie, Unité du Sommeil, CHU Montpellier, Hôpital Gui–de–Chauliac Université de Montpellier, INSERM INM Montpellier France

Abstract

SummarySleep architecture encodes relevant information on the structure of sleep and has been used to assess hyperarousal in insomnia. This study investigated whether polysomnography‐derived sleep architecture displays signs of hyperarousal in individuals with insomnia compared with individuals without insomnia. Data from Phase 3 clinical trials, private clinics and a cohort study were analysed. A comprehensive set of sleep architecture features previously associated with hyperarousal were retrospectively analysed focusing on sleep–wake transition probabilities, electroencephalographic spectra and sleep spindles, and enriched with a novel machine learning algorithm called the Wake Electroencephalographic Similarity Index. This analysis included 1710 individuals with insomnia and 1455 individuals without insomnia. Results indicate that individuals with insomnia had a higher likelihood of waking from all sleep stages, and showed increased relative alpha during Wake and N1 sleep and increased theta power during Wake when compared with individuals without insomnia. Relative delta power was decreased and Wake Electroencephalographic Similarity Index scores were elevated across all sleep stages except N3, suggesting more wake‐like activity during these stages in individuals with insomnia. Additionally, sleep spindle density was decreased, and spindle dispersion was increased in individuals with insomnia. These findings suggest that insomnia is characterized by a dysfunction in sleep quality with a continuous hyperarousal, evidenced by changes in sleep–wake architecture.

Publisher

Wiley

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