Physiological Markers of Arousal Change with Psychological Treatment for Insomnia: A Preliminary Investigation

PLoS One. 2015 Dec 18;10(12):e0145317. doi: 10.1371/journal.pone.0145317. eCollection 2015.

Abstract

Objectives: The aim of this preliminary study was to evaluate if Sleep Restriction Therapy for insomnia is associated with modifications to physiological arousal, indexed through overnight measures of plasma cortisol concentrations and core body temperature.

Methods: In a pre-to-post open label study design, eleven patients with chronic and severe Psychophysiological Insomnia underwent 5 weeks of Sleep Restriction Therapy.

Results: Eight (73%) patients out of 11 consented completed therapy and showed a decrease in insomnia severity pre-to-post treatment (mean (SD): 18.1 (2.8) versus 8.4 (4.8); p = .001). Six patients were analyzed with pre-to-post overnight measures of temperature and cortisol. Contrary to our hypothesis, significantly higher levels of plasma cortisol concentrations were found during the early morning at post-treatment compared to baseline (p < .01), while no change was observed in the pre-sleep phase or early part of the night. Core body temperature during sleep was however reduced significantly (overall mean [95% CI]: 36.54 (°C) [36.3, 36.8] versus 36.45 [36.2, 36.7]; p < .05).

Conclusions: Sleep Restriction Therapy therefore was associated with increased early morning cortisol concentrations and decreased core body temperature, supporting the premise of physiological changes in functioning after effective therapy. Future work should evaluate change in physiological variables associated with clinical treatment response.

Trial registration: Australian New Zealand Clinical Trials Registry ANZCTR 12612000049875.

Publication types

  • Clinical Trial
  • Research Support, Non-U.S. Gov't

MeSH terms

  • Adult
  • Arousal
  • Biomarkers / blood
  • Body Temperature
  • Circadian Rhythm
  • Female
  • Humans
  • Hydrocortisone / blood*
  • Male
  • Middle Aged
  • Sleep
  • Sleep Initiation and Maintenance Disorders / blood
  • Sleep Initiation and Maintenance Disorders / therapy*
  • Treatment Outcome

Substances

  • Biomarkers
  • Hydrocortisone

Associated data

  • ANZCTR/ANZCTR12612000049875

Grants and funding

This research was supported by the National Health and Medical Research Council (NHMRC, Australia) Centres for Integrated Research and Understanding of Sleep (CIRUS) 571421 & NeuroSleep 1060992; the Sackler Institute of Psychobiological Research (University of Glasgow Sleep Centre, Scotland, UK); and the Chief Scientist Office (Scotland, UK) CZG/2/503. The funders had no role in study design, data collection and analysis, decision to publish, or preparation of the manuscript.