HPA axis function and diurnal cortisol in post-traumatic stress disorder: A systematic review

Background: There is inconsistency in the literature regarding the nature of hypothalamic-pituitary-adrenal (HPA) axis functionality in post-traumatic stress disorder (PTSD). Purpose: The review aimed to investigate HPA axis functionality via the diurnal profile of cortisol as it relates to PTSD. Me...

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Main Authors: Kathryn E. Speer, Stuart Semple, Nenad Naumovski, Nathan M. D'Cunha, Andrew J. McKune
Format: Article
Language:English
Published: Elsevier 2019-11-01
Series:Neurobiology of Stress
Online Access:http://www.sciencedirect.com/science/article/pii/S2352289518301085
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author Kathryn E. Speer
Stuart Semple
Nenad Naumovski
Nathan M. D'Cunha
Andrew J. McKune
author_facet Kathryn E. Speer
Stuart Semple
Nenad Naumovski
Nathan M. D'Cunha
Andrew J. McKune
author_sort Kathryn E. Speer
collection DOAJ
description Background: There is inconsistency in the literature regarding the nature of hypothalamic-pituitary-adrenal (HPA) axis functionality in post-traumatic stress disorder (PTSD). Purpose: The review aimed to investigate HPA axis functionality via the diurnal profile of cortisol as it relates to PTSD. Methods: The authors conducted a systematic review of the literature from June 2017 – March 2019 in accordance with The PRISMA Statement in the following four databases: PubMed, MEDLINE, ScienceDirect and PsycINFO with Full Text. The search strategy was limited to articles in English language, published in peer-reviewed journals within the last decade and human studies. Search terms included “post-traumatic stress disorder” OR “PTSD”, AND “hypothalamic pituitary adrenal axis” OR “HPA axis” AND “diurnal cortisol” OR “cortisol”. PTSD sufferers of all trauma types, genders and socioeconomic statuses were included provided there was a “healthy” control group and an inclusion of reporting on inter-group measurements of diurnal cortisol profiles as a portrayal of HPA axis functionality. Results: A total of 10 studies met the criteria for inclusion in this review. The association between HPA axis functionality and PTSD was evaluated by the measurement of salivary and/or plasma cortisol concentrations. Only two studies demonstrated an association between PTSD and diurnal cortisol when compared with respective control groups while three studies found no associations. The remaining five studies found partial, mostly negative associations between PTSD and diurnal cortisol. Conclusion: Despite some indications of an association between PTSD and dysregulated HPA axis functionality as demonstrated by diurnal cortisol output, the current review has revealed mixed findings. As such, a complete understanding of HPA axis dysregulation as it relates to PTSD remains unestablished. Given the findings, further investigation into the relationship between PTSD trauma-exposed and non-PTSD trauma-exposed individuals and diurnal cortisol is warranted.
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spelling doaj.art-9e1586b744674bca8c90f126ac2f10572022-12-21T19:43:30ZengElsevierNeurobiology of Stress2352-28952019-11-0111HPA axis function and diurnal cortisol in post-traumatic stress disorder: A systematic reviewKathryn E. Speer0Stuart Semple1Nenad Naumovski2Nathan M. D'Cunha3Andrew J. McKune4Discipline of Sport and Exercise Science, Faculty of Health, University of Canberra, Canberra, ACT, 2601, Australia; Research Institute for Sport and Exercise, University of Canberra, Canberra, ACT, 2601, Australia; Collaborative Research in Bioactives and Biomarkers (CRIBB) Group, University of Canberra, Bruce, ACT, 2617, Australia; Corresponding author. University of Canberra Research Institute for Sport and Exercise (UCRISE), Canberra, ACT, 2601, Australia.Discipline of Sport and Exercise Science, Faculty of Health, University of Canberra, Canberra, ACT, 2601, Australia; Research Institute for Sport and Exercise, University of Canberra, Canberra, ACT, 2601, AustraliaFaculty of Health, University of Canberra, Canberra, ACT, 2601, Australia; Collaborative Research in Bioactives and Biomarkers (CRIBB) Group, University of Canberra, Bruce, ACT, 2617, Australia; University of Canberra Health Research Institute (UC-HRI), Canberra, ACT, 2617, AustraliaFaculty of Health, University of Canberra, Canberra, ACT, 2601, Australia; Collaborative Research in Bioactives and Biomarkers (CRIBB) Group, University of Canberra, Bruce, ACT, 2617, AustraliaDiscipline of Sport and Exercise Science, Faculty of Health, University of Canberra, Canberra, ACT, 2601, Australia; Research Institute for Sport and Exercise, University of Canberra, Canberra, ACT, 2601, Australia; Discipline of Biokinetics, Exercise and Leisure Sciences, School of Health Sciences, University of KwaZulu-Natal, Durban, KwaZulu-Natal, 4000, South Africa; Collaborative Research in Bioactives and Biomarkers (CRIBB) Group, University of Canberra, Bruce, ACT, 2617, AustraliaBackground: There is inconsistency in the literature regarding the nature of hypothalamic-pituitary-adrenal (HPA) axis functionality in post-traumatic stress disorder (PTSD). Purpose: The review aimed to investigate HPA axis functionality via the diurnal profile of cortisol as it relates to PTSD. Methods: The authors conducted a systematic review of the literature from June 2017 – March 2019 in accordance with The PRISMA Statement in the following four databases: PubMed, MEDLINE, ScienceDirect and PsycINFO with Full Text. The search strategy was limited to articles in English language, published in peer-reviewed journals within the last decade and human studies. Search terms included “post-traumatic stress disorder” OR “PTSD”, AND “hypothalamic pituitary adrenal axis” OR “HPA axis” AND “diurnal cortisol” OR “cortisol”. PTSD sufferers of all trauma types, genders and socioeconomic statuses were included provided there was a “healthy” control group and an inclusion of reporting on inter-group measurements of diurnal cortisol profiles as a portrayal of HPA axis functionality. Results: A total of 10 studies met the criteria for inclusion in this review. The association between HPA axis functionality and PTSD was evaluated by the measurement of salivary and/or plasma cortisol concentrations. Only two studies demonstrated an association between PTSD and diurnal cortisol when compared with respective control groups while three studies found no associations. The remaining five studies found partial, mostly negative associations between PTSD and diurnal cortisol. Conclusion: Despite some indications of an association between PTSD and dysregulated HPA axis functionality as demonstrated by diurnal cortisol output, the current review has revealed mixed findings. As such, a complete understanding of HPA axis dysregulation as it relates to PTSD remains unestablished. Given the findings, further investigation into the relationship between PTSD trauma-exposed and non-PTSD trauma-exposed individuals and diurnal cortisol is warranted.http://www.sciencedirect.com/science/article/pii/S2352289518301085
spellingShingle Kathryn E. Speer
Stuart Semple
Nenad Naumovski
Nathan M. D'Cunha
Andrew J. McKune
HPA axis function and diurnal cortisol in post-traumatic stress disorder: A systematic review
Neurobiology of Stress
title HPA axis function and diurnal cortisol in post-traumatic stress disorder: A systematic review
title_full HPA axis function and diurnal cortisol in post-traumatic stress disorder: A systematic review
title_fullStr HPA axis function and diurnal cortisol in post-traumatic stress disorder: A systematic review
title_full_unstemmed HPA axis function and diurnal cortisol in post-traumatic stress disorder: A systematic review
title_short HPA axis function and diurnal cortisol in post-traumatic stress disorder: A systematic review
title_sort hpa axis function and diurnal cortisol in post traumatic stress disorder a systematic review
url http://www.sciencedirect.com/science/article/pii/S2352289518301085
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