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Sleep, a Governor of Morbidity in PTSD: A Systematic Review of Biological Markers in PTSD-Related Sleep Disturbances.
Maguire, Daniel G; Ruddock, Mark W; Milanak, Melissa E; Moore, Tara; Cobice, Diego; Armour, Cherie.
Affiliation
  • Maguire DG; Biomedical Sciences Research Institute, Ulster University, Coleraine BT52 1SA, Northern Ireland.
  • Ruddock MW; Randox Laboratories Ltd, Clinical Studies, Crumlin, County Antrim BT29 4QY, Northern Ireland.
  • Milanak ME; Department of Psychiatry & Behavioral Sciences, Medical University of South Carolina, Charleston, SC 29425, USA.
  • Moore T; Biomedical Sciences Research Institute, Ulster University, Coleraine BT52 1SA, Northern Ireland.
  • Cobice D; Biomedical Sciences Research Institute, Ulster University, Coleraine BT52 1SA, Northern Ireland.
  • Armour C; School of Psychology, David Keir Building, Queen's University Belfast, Belfast BT9 5BN, Northern Ireland.
Nat Sci Sleep ; 12: 545-562, 2020.
Article in En | MEDLINE | ID: mdl-32801980
ABSTRACT

BACKGROUND:

Sleep disturbances (SD) are the most impactful and commonly reported symptoms in post-traumatic stress disorder (PTSD). Yet, they are often resistant to primary PTSD therapies. Research has identified two distinct SDs highly prevalent in PTSD; insomnia and nightmares. Those who report SDs prior to a traumatic event are at greater risk for developing PTSD; highlighting that sleep potentially plays a role in PTSD's pathology. To further understand the pathobiological mechanisms that lead to the development of PTSD, it is first imperative to understand the interplay which exists between sleep and PTSD on a biological level. The aim of this systematic review is to determine if biological or physiological markers are related to SD in PTSD.

METHODS:

A systematic literature search was conducted on the electronic databases; Medline, Embase, AMED and PsycINFO, using Medical Subject Headings and associated keywords.

RESULTS:

Sixteen studies were included in the final analyses. Physiological makers of autonomic function, and biochemical markers of HPA-axis activity; inflammatory processes; and trophic factor regulation were related to the severity of SDs in PTSD.

CONCLUSION:

These findings add to the growing literature base supporting a central focus on sleep in research aiming to define the pathophysiological processes which result in PTSD, as well as emphasising the importance of specifically targeting sleep as part of a successful PTSD intervention strategy. Resolving SDs will not only reduce PTSD symptom severity and improve quality of life but will also reduce all-cause mortality, hospital admissions and lifetime healthcare costs for those with PTSD. Limitations of the current literature are discussed, and key recommendations future research must adhere to are made within.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Guideline / Prognostic_studies / Systematic_reviews Aspects: Patient_preference Language: En Journal: Nat Sci Sleep Year: 2020 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Type of study: Guideline / Prognostic_studies / Systematic_reviews Aspects: Patient_preference Language: En Journal: Nat Sci Sleep Year: 2020 Document type: Article