Does prior traumatization affect the treatment outcome of CBT for panic disorder? The potential role of the MAOA gene and depression symptoms.


Journal

European archives of psychiatry and clinical neuroscience
ISSN: 1433-8491
Titre abrégé: Eur Arch Psychiatry Clin Neurosci
Pays: Germany
ID NLM: 9103030

Informations de publication

Date de publication:
Mar 2019
Historique:
received: 01 10 2016
accepted: 09 07 2017
pubmed: 18 7 2017
medline: 21 6 2019
entrez: 17 7 2017
Statut: ppublish

Résumé

Although cognitive behavioral therapy (CBT) is highly effective in the treatment of anxiety disorders, many patients still do not benefit. This study investigates whether a history of traumatic event experience is negatively associated with outcomes of CBT for panic disorder. The moderating role of the monoamine oxidase A (MAOA) gene and depression symptoms as well as the association between trauma history and fear reactivity as a potential mechanism are further analyzed. We conducted a post-hoc analysis of 172 male and 60 female patients with panic disorder treated with CBT in a multi-center study. Treatment outcome was assessed at post-treatment using self-report and clinician rating scales. Fear reactivity before treatment was assessed via heart rate and self-reported anxiety during a behavioral avoidance test. Among females, we did not find any differences in treatment response between traumatized and non-traumatized individuals or any two-way interaction trauma history × MAOA genotype. There was a significant three-way interaction trauma history × MAOA genotype × depression symptoms on all treatment outcomes indicating that in traumatized female patients carrying the low-activity allele, treatment effect sizes decreased with increasing depression symptoms at baseline. No such effects were observed for males. In conclusion, we found no evidence for a differential treatment response in traumatized and non-traumatized individuals. There is preliminary evidence for poorer treatment outcomes in a subgroup of female traumatized individuals carrying the low-active variant of the MAOA gene. These patients also report more symptoms of depression symptomatology and exhibit a dampened fear response before treatment which warrants further investigation.

Identifiants

pubmed: 28712090
doi: 10.1007/s00406-017-0823-9
pii: 10.1007/s00406-017-0823-9
doi:

Substances chimiques

Monoamine Oxidase EC 1.4.3.4
monoamine oxidase A, human EC 1.4.3.4.

Types de publication

Journal Article Multicenter Study Randomized Controlled Trial

Langues

eng

Sous-ensembles de citation

IM

Pagination

161-170

Subventions

Organisme : German Federal Ministry of Education and Research
ID : 01GV0615

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Auteurs

Sebastian Trautmann (S)

Institute of Clinical Psychology and Psychotherapy, Technische Universität Dresden, Chemnitzer Str. 46, 01187, Dresden, Germany. Sebastian.Trautmann1@tu-dresden.de.

Jan Richter (J)

Department of Biological and Clinical Psychology, University of Greifswald, Greifswald, Germany.

Markus Muehlhan (M)

Institute of Clinical Psychology and Psychotherapy, Technische Universität Dresden, Chemnitzer Str. 46, 01187, Dresden, Germany.
Department of Psychology, Faculty of Human Science, Medical School Hamburg, Hamburg, Germany.

Michael Höfler (M)

Institute of Clinical Psychology and Psychotherapy, Technische Universität Dresden, Chemnitzer Str. 46, 01187, Dresden, Germany.

Hans-Ulrich Wittchen (HU)

Institute of Clinical Psychology and Psychotherapy, Technische Universität Dresden, Chemnitzer Str. 46, 01187, Dresden, Germany.
Clinical Psychology and Psychotherapy RG, Department of Psychiatry and Psychotherapy, Ludwig Maximilans Universität Munich, Munich, Germany.

Katharina Domschke (K)

Department of Psychiatry, Psychosomatics, and Psychotherapy, University of Würzburg, Würzburg, Germany.
Department of Psychiatry and Psychotherapy, Medical Center - University of Freiburg, Faculty of Medicine, University of Freiburg, Freiburg, Germany.

Andreas Ströhle (A)

Department of Psychiatry and Psychotherapy, Campus Charité Mitte, Charité-Universitätsmedizin Berlin, Berlin, Germany.

Alfons O Hamm (AO)

Department of Biological and Clinical Psychology, University of Greifswald, Greifswald, Germany.

Heike Weber (H)

Department of Psychiatry, Psychosomatics, and Psychotherapy, University of Würzburg, Würzburg, Germany.
Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, Goethe-University Frankfurt, Frankfurt, Germany.

Tilo Kircher (T)

Department of Psychiatry and Psychotherapy, Philipps-University Marburg, Marburg, Germany.

Volker Arolt (V)

Department of Psychiatry and Psychotherapy, University of Muenster, Muenster, Germany.

Alexander L Gerlach (AL)

Department of Clinical Psychology and Psychotherapy, University of Cologne, Cologne, Germany.

Georg W Alpers (GW)

Psychology, School of Social Sciences, University of Mannheim, Mannheim, Germany.

Thomas Fydrich (T)

Institute of Psychology, Humboldt-University, Berlin, Germany.

Thomas Lang (T)

Christoph-Dornier-Foundation for Clinical Psychology, Bremen, Germany.
Department of Clinical Psychology and Psychotherapy, University of Hamburg, Hamburg, Germany.

Andreas Reif (A)

Department of Psychiatry, Psychosomatic Medicine and Psychotherapy, Goethe-University Frankfurt, Frankfurt, Germany.

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Classifications MeSH