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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.
Weber, Heike; 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; Avdibegovic, Esmina; Agani, Ferid; Warrings, Bodo; Domschke, Katharina; Nievergelt, Caroline M; Deckert, Jürgen; Dzubur-Kulenovic, Alma; Erhardt, Angelika.
Afiliación
  • Weber H; Department of Psychiatry, Psychosomatics and Psychotherapy, Centre of Mental Health, Julius-Maximilians-University, Margarete-Höppel-Platz 1, 97080, Würzburg, Germany. Weber_H2@ukw.de.
  • Maihofer AX; Department of Psychiatry, University of California San Diego, La Jolla, CA, USA.
  • Jaksic N; Department of Psychiatry and Psychological Medicine, University Hospital Center Zagreb, Zagreb, Croatia.
  • Bojic EF; Department for Genetic and Biotechnology, International Burch University, Sarajevo, Bosnia and Herzegovina.
  • Kucukalic S; Department of Psychiatry, University Clinical Center, Sarajevo, Bosnia and Herzegovina.
  • Dzananovic ES; Department of Psychiatry, University Clinical Center, Sarajevo, Bosnia and Herzegovina.
  • Uka AG; Department of Psychiatry, University Clinical Center of Kosovo, Prishtina, Kosovo.
  • Hoxha B; Department of Psychiatry, University Clinical Center of Kosovo, Prishtina, Kosovo.
  • Haxhibeqiri V; Department of Medical Biochemistry, University Clinical Center of Kosovo, Prishtina, Kosovo.
  • Haxhibeqiri S; Institute of Kosovo Forensic Psychiatry, University Clinical Center of Kosovo, Prishtina, Kosovo.
  • Kravic N; Department of Psychiatry, University Clinical Center of Tuzla, Tuzla, Bosnia and Herzegovina.
  • Umihanic MM; Community Health Center, Zivinice, Bosnia and Herzegovina.
  • Franc AC; Department of Psychiatry and Psychological Medicine, University Hospital Center Zagreb, Zagreb, Croatia.
  • Babic R; Department of Psychiatry, University Clinical Center of Mostar, Mostar, Bosnia and Herzegovina.
  • Pavlovic M; Department of Psychiatry, University Clinical Center of Mostar, Mostar, Bosnia and Herzegovina.
  • Mehmedbasic AB; Department of Psychiatry, University Clinical Center, Sarajevo, Bosnia and Herzegovina.
  • Aukst-Margetic B; Department of Psychiatry, University Hospital Sestre Milosrdnice, Zagreb, Croatia.
  • Kucukalic A; Department of Psychiatry, University Clinical Center, Sarajevo, Bosnia and Herzegovina.
  • Marjanovic D; Department for Genetic and Biotechnology, International Burch University, Sarajevo, Bosnia and Herzegovina.
  • Babic D; Center for Applied Bioanthropology, Institute for Anthropological Researches, Zagreb, Croatia.
  • Bozina N; Department of Psychiatry, University Clinical Center of Mostar, Mostar, Bosnia and Herzegovina.
  • Jakovljevic M; Department of Laboratory Diagnostics, University Hospital Center Zagreb, Zagreb, Croatia.
  • Sinanovic O; Department of Psychiatry and Psychological Medicine, University Hospital Center Zagreb, Zagreb, Croatia.
  • Avdibegovic E; Department of Neurology, University Clinical Center of Tuzla, Tuzla, Bosnia and Herzegovina.
  • Agani F; Department of Psychiatry, University Clinical Center of Tuzla, Tuzla, Bosnia and Herzegovina.
  • Warrings B; Faculty of Medicine, University Hasan Prishtina, Prishtina, Kosovo.
  • Domschke K; Department of Psychiatry, Psychosomatics and Psychotherapy, Centre of Mental Health, Julius-Maximilians-University, Margarete-Höppel-Platz 1, 97080, Würzburg, Germany.
  • Nievergelt CM; Department of Psychiatry and Psychotherapy, Medical Center-University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.
  • Deckert J; Department of Psychiatry, University of California San Diego, La Jolla, CA, USA.
  • Dzubur-Kulenovic A; Department of Psychiatry, Psychosomatics and Psychotherapy, Centre of Mental Health, Julius-Maximilians-University, Margarete-Höppel-Platz 1, 97080, Würzburg, Germany.
  • Erhardt A; Department of Psychiatry, University Clinical Center, Sarajevo, Bosnia and Herzegovina.
J Neural Transm (Vienna) ; 129(5-6): 661-674, 2022 06.
Article en En | MEDLINE | ID: mdl-34837533
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.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastornos por Estrés Postraumático Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: J Neural Transm (Vienna) Año: 2022 Tipo del documento: Article País de afiliación: Alemania

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Trastornos por Estrés Postraumático Tipo de estudio: Diagnostic_studies / Etiology_studies / Observational_studies / Risk_factors_studies Límite: Humans País/Región como asunto: Europa Idioma: En Revista: J Neural Transm (Vienna) Año: 2022 Tipo del documento: Article País de afiliación: Alemania