dc.contributor.author
Engel, Sinha
dc.contributor.author
Laufer, Sebastian
dc.contributor.author
Klusmann, Hannah
dc.contributor.author
Schulze, Lars
dc.contributor.author
Schumacher, Sarah
dc.contributor.author
Knaevelsrud, Christine
dc.date.accessioned
2023-08-09T12:22:49Z
dc.date.available
2023-08-09T12:22:49Z
dc.identifier.uri
https://refubium.fu-berlin.de/handle/fub188/40399
dc.identifier.uri
http://dx.doi.org/10.17169/refubium-40120
dc.description.abstract
Background: Pre-and post-traumatic hypothalamic–pituitary–adrenal (HPA) axis markers have been studied to predict posttraumatic stress disorder (PTSD) risk, but its acute reactivity cannot be measured in real-life settings. Experimental paradigms can depict the cortisol response to stimuli that simulate traumatic events.
Objective: To review experimental studies on the cortisol response to traumatic stimuli and the correlation between cortisol and PTSD symptoms.
Method: Experimental, (un-)published studies in German or English from any year were eligible if they confronted non-traumatized humans with traumatic stimuli, assessed cortisol before, during or after stimulus presentation and subsequent PTSD symptoms. The literature was searched via PubMed, PubPsych, PsychINFO, PsycArticle, Web of Science, EMBASE, ProQuest and ClinicalTrials.gov up to 16th February 2021. Risk of bias was assessed with the Cortisol Assessment List. Multilevel-meta-analyses were conducted under the random effects model. The standardized mean change (dSMC) indicated the cortisol response. Coefficient r indicated the correlations between cortisol and PTSD symptoms.
Results: 14 studies, investigating 1004 individuals, were included. A cortisol response was successfully induced between 21 and 40 min post-presentation onset (kobservations = 25, dSMC = 0.15 [.03; .26]). Cortisol was not associated with overall or cluster-level PTSD symptoms. On a symptom-level, higher pre-presentation onset cortisol was correlated with lower state tension (k = 8, r = −.18 [−.35; −.01]), higher state happiness (k = 8, r = −.34 [−.59; −.03], variable inverted) and lower state anger (k = 9, r = −.14 [−.26; −.01]). Higher post-presentation onset cortisol was correlated with higher state happiness (k = 16, r = −.20 [−.33; −.06]) and lower state sadness (k = 17, r = −.16 [−.25; −.05]), whereas cortisol response was positively correlated with state anxiety (k = 9, r = .16 [0.04; 0.27]).
Conclusions: Experimental paradigms effectively induce a cortisol response. Higher basal cortisol, higher cortisol, as measured after traumatic stimulus presentation, and a lower cortisol response were associated with more adaptive emotional reactions. These markers did not predict longer-term PTSD symptoms.
en
dc.format.extent
16 Seiten
dc.rights.uri
https://creativecommons.org/licenses/by-nc/4.0/
dc.subject
Prognostic biomarker
en
dc.subject
glucocorticoid
en
dc.subject.ddc
100 Philosophie und Psychologie::150 Psychologie::150 Psychologie
dc.title
Cortisol response to traumatic stress to predict PTSD symptom development – a systematic review and meta-analysis of experimental studies
dc.type
Wissenschaftlicher Artikel
dcterms.bibliographicCitation.articlenumber
2225153
dcterms.bibliographicCitation.doi
10.1080/20008066.2023.2225153
dcterms.bibliographicCitation.journaltitle
European Journal of Psychotraumatology
dcterms.bibliographicCitation.number
2
dcterms.bibliographicCitation.volume
14
dcterms.bibliographicCitation.url
https://doi.org/10.1080/20008066.2023.2225153
refubium.affiliation
Erziehungswissenschaft und Psychologie
refubium.affiliation.other
Arbeitsbereich Klinisch-Psychologische Intervention
refubium.affiliation.other
Arbeitsbereich Klinische Psychologie und Psychotherapie
refubium.funding
Taylor Francis
refubium.note.author
We acknowledge support by the Open Access Publication Fund of the Freie Universität Berlin.
refubium.resourceType.isindependentpub
no
dcterms.accessRights.openaire
open access
dcterms.isPartOf.eissn
2000-8066
refubium.resourceType.provider
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