4.7 Article

Sleep disturbance and melatonin levels following traumatic brain injury

Journal

NEUROLOGY
Volume 74, Issue 21, Pages 1732-1738

Publisher

LIPPINCOTT WILLIAMS & WILKINS
DOI: 10.1212/WNL.0b013e3181e0438b

Keywords

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Funding

  1. National Health and Medical Research Council
  2. NHMRC
  3. Victorian Neurotrauma Initiative
  4. Monash University
  5. Jack Brockhoff Foundation
  6. Vanda Pharmaceuticals
  7. Takeda Pharmaceutical Company Limited
  8. ResMed Foundation
  9. Respironics Sleep and Respiratory Research Foundation
  10. Cephalon, Inc.
  11. Philips Lighting
  12. Department of Homeland Security-Federal Emergency Management Agency (FEMA)
  13. Australia-India Council
  14. NIH (NHLBI) [R01 HL093279]
  15. Royal Australasian College of General Practitioners/Centre of National Research on Disability and Rehabilitation Medicine
  16. Centers for Disease Control and Prevention
  17. National Institute of Justice

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Objectives: Sleep disturbances commonly follow traumatic brain injury (TBI) and contribute to ongoing disability. However, there are no conclusive findings regarding specific changes to sleep quality and sleep architecture measured using polysomnography. Possible causes of the sleep disturbances include disruption of circadian regulation of sleep-wakefulness, psychological distress, and a neuronal response to injury. We investigated sleep-wake disturbances and their underlying mechanisms in a TBI patient sample. Methods: This was an observational study comparing 23 patients with TBI (429.7 +/- 287.6 days post injury) and 23 age- and gender-matched healthy volunteers on polysomnographic sleep measures, salivary dim light melatonin onset (DLMO) time, and self-reported sleep quality, anxiety, and depression. Results: Patients with TBI reported higher anxiety and depressive symptoms and sleep disturbance than controls. Patients with TBI showed decreased sleep efficiency (SE) and increased wake after sleep onset (WASO). Although no significant group differences were found in sleep architecture, when anxiety and depression scores were controlled, patients with TBI showed higher amount of slow wave sleep. No differences in self-reported sleep timing or salivary DLMO time were found. However, patients with TBI showed significantly lower levels of evening melatonin production. Melatonin level was significantly correlated with REM sleep but not SE or WASO. Conclusions: Reduced evening melatonin production may indicate disruption to circadian regulation of melatonin synthesis. The results suggest that there are at least 2 factors contributing to sleep disturbances in patients with traumatic brain injury. We propose that elevated depression is associated with reduced sleep quality, and increased slow wave sleep is attributed to the effects of mechanical brain damage. Neurology (R) 2010; 74: 1732-1738

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