Association of polygenic risk scores, traumatic life events and coping strategies with war-related PTSD diagnosis and symptom severity in the South Eastern Europe (SEE)-PTSD cohort

Author:

Weber HeikeORCID,Maihofer Adam X.,Jaksic Nenad,Bojic Elma Feric,Kucukalic Sabina,Dzananovic Emina Sabic,Uka Aferdita Goci,Hoxha Blerina,Haxhibeqiri Valdete,Haxhibeqiri Shpend,Kravic Nermina,Umihanic Mirnesa Muminovic,Franc Ana Cima,Babic Romana,Pavlovic Marko,Mehmedbasic Alma Bravo,Aukst-Margetic Branka,Kucukalic Abdulah,Marjanovic Damir,Babic Dragan,Bozina Nada,Jakovljevic Miro,Sinanovic Osman,Avdibegović Esmina,Agani Ferid,Warrings Bodo,Domschke Katharina,Nievergelt Caroline M.,Deckert Jürgen,Dzubur-Kulenovic Alma,Erhardt Angelika

Abstract

Abstract Objectives Posttraumatic stress disorder (PTSD) is triggered by extremely stressful environmental events and characterized by high emotional distress, re-experiencing of trauma, avoidance and hypervigilance. The present study uses polygenic risk scores (PRS) derived from the UK Biobank (UKBB) mega-cohort analysis as part of the PGC PTSD GWAS effort to determine the heritable basis of PTSD in the South Eastern Europe (SEE)-PTSD cohort. We further analyzed the relation between PRS and additional disease-related variables, such as number and intensity of life events, coping, sex and age at war on PTSD and CAPS as outcome variables. Methods Association of PRS, number and intensity of life events, coping, sex and age on PTSD were calculated using logistic regression in a total of 321 subjects with current and remitted PTSD and 337 controls previously subjected to traumatic events but not having PTSD. In addition, PRS and other disease-related variables were tested for association with PTSD symptom severity, measured by the Clinician Administrated PTSD Scale (CAPS) by liner regression. To assess the relationship between the main outcomes PTSD diagnosis and symptom severity, each of the examined variables was adjusted for all other PTSD related variables. Results The categorical analysis showed significant polygenic risk in patients with remitted PTSD and the total sample, whereas no effects were found on symptom severity. Intensity of life events as well as the individual coping style were significantly associated with PTSD diagnosis in both current and remitted cases. The dimensional analyses showed as association of war-related frequency of trauma with symptom severity, whereas the intensity of trauma yielded significant results independently of trauma timing in current PTSD. Conclusions The present PRS application in the SEE-PTSD cohort confirms modest but significant polygenic risk for PTSD diagnosis. Environmental factors, mainly the intensity of traumatic life events and negative coping strategies, yielded associations with PTSD both categorically and dimensionally with more significant p-values. This suggests that, at least in the present cohort of war-related trauma, the association of environmental factors and current individual coping strategies with PTSD psychopathology was stronger than the polygenic risk.

Funder

Deutsche Forschungsgemeinschaft

National Institute on Minority Health and Health Disparities

Universitätsklinikum Würzburg

Publisher

Springer Science and Business Media LLC

Subject

Biological Psychiatry,Psychiatry and Mental health,Clinical Neurology,Neurology

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