The Risk of Posttraumatic Stress Disorder After Trauma Depends on Traumatic Load and the Catechol-O-Methyltransferase Val158Met Polymorphism

Lade...
Vorschaubild
Dateien
Kolassa_etal_2010_BiologicalPsychiatry.pdf
Kolassa_etal_2010_BiologicalPsychiatry.pdfGröße: 540.22 KBDownloads: 1384
Datum
2010
Autor:innen
Kolassa, Stephan
Papassotiropoulos, Andreas
Quervain, Dominique J.-F. de
Herausgeber:innen
Kontakt
ISSN der Zeitschrift
Electronic ISSN
ISBN
Bibliografische Daten
Verlag
Schriftenreihe
Auflagebezeichnung
ArXiv-ID
Internationale Patentnummer
Angaben zur Forschungsförderung
Projekt
Stress and trauma-associated immunological changes and their implications on health
Open Access-Veröffentlichung
Open Access Green
Core Facility der Universität Konstanz
Gesperrt bis
Titel in einer weiteren Sprache
Forschungsvorhaben
Organisationseinheiten
Zeitschriftenheft
Publikationstyp
Zeitschriftenartikel
Publikationsstatus
Published
Erschienen in
Biological Psychiatry. 2010, 67(4), pp. 304-308. Available under: doi: 10.1016/j.biopsych.2009.10.009
Zusammenfassung

Background
The risk for posttraumatic stress disorder (PTSD) depends on the number of traumatic event types experienced in a dose response relationship, but genetic factors are known to also influence the risk of PTSD. The catechol-O-methyltransferase (COMT) Val158Met polymorphism has been found to affect fear extinction and might play a role in the etiology of anxiety disorders.
Methods
Traumatic load and lifetime and current diagnosis of PTSD and COMT genotype were assessed in a sample of 424 survivors of the Rwandan Genocide living in the Nakivale refugee camp in southwestern Uganda.
Results
Higher numbers of different lifetime traumatic event types led to a higher prevalence of lifetime PTSD in a dose response relationship. However, this effect was modulated by the COMT genotype: whereas Val allele carriers showed the typical dose response relationship, Met/Met homozygotes exhibited a high risk for PTSD independently of the severity of traumatic load.
Conclusions
The present findings indicate a gene environment interaction between the human COMT Val158Met polymorphism and the number of traumatic event types experienced in the risk of developing PTSD.

Zusammenfassung in einer weiteren Sprache
Fachgebiet (DDC)
150 Psychologie
Schlagwörter
COMT polymorphism, genetic polymorphisms, post-traumatic stress disorder, refugees, risk
Konferenz
Rezension
undefined / . - undefined, undefined
Zitieren
ISO 690KOLASSA, Iris-Tatjana, Stephan KOLASSA, Verena ERTL, Andreas PAPASSOTIROPOULOS, Dominique J.-F. de QUERVAIN, 2010. The Risk of Posttraumatic Stress Disorder After Trauma Depends on Traumatic Load and the Catechol-O-Methyltransferase Val158Met Polymorphism. In: Biological Psychiatry. 2010, 67(4), pp. 304-308. Available under: doi: 10.1016/j.biopsych.2009.10.009
BibTex
@article{Kolassa2010Postt-10635,
  year={2010},
  doi={10.1016/j.biopsych.2009.10.009},
  title={The Risk of Posttraumatic Stress Disorder After Trauma Depends on Traumatic Load and the Catechol-O-Methyltransferase Val158Met Polymorphism},
  number={4},
  volume={67},
  journal={Biological Psychiatry},
  pages={304--308},
  author={Kolassa, Iris-Tatjana and Kolassa, Stephan and Ertl, Verena and Papassotiropoulos, Andreas and Quervain, Dominique J.-F. de}
}
RDF
<rdf:RDF
    xmlns:dcterms="http://purl.org/dc/terms/"
    xmlns:dc="http://purl.org/dc/elements/1.1/"
    xmlns:rdf="http://www.w3.org/1999/02/22-rdf-syntax-ns#"
    xmlns:bibo="http://purl.org/ontology/bibo/"
    xmlns:dspace="http://digital-repositories.org/ontologies/dspace/0.1.0#"
    xmlns:foaf="http://xmlns.com/foaf/0.1/"
    xmlns:void="http://rdfs.org/ns/void#"
    xmlns:xsd="http://www.w3.org/2001/XMLSchema#" > 
  <rdf:Description rdf:about="https://kops.uni-konstanz.de/server/rdf/resource/123456789/10635">
    <dc:language>eng</dc:language>
    <foaf:homepage rdf:resource="http://localhost:8080/"/>
    <dc:contributor>Papassotiropoulos, Andreas</dc:contributor>
    <dc:rights>terms-of-use</dc:rights>
    <dc:contributor>Quervain, Dominique J.-F. de</dc:contributor>
    <dcterms:issued>2010</dcterms:issued>
    <dcterms:title>The Risk of Posttraumatic Stress Disorder After Trauma Depends on Traumatic Load and the Catechol-O-Methyltransferase Val158Met Polymorphism</dcterms:title>
    <dspace:hasBitstream rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/10635/1/Kolassa_etal_2010_BiologicalPsychiatry.pdf"/>
    <dc:format>application/pdf</dc:format>
    <dcterms:available rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-25T09:20:16Z</dcterms:available>
    <dc:creator>Kolassa, Stephan</dc:creator>
    <dcterms:abstract xml:lang="eng">Background&lt;br /&gt;The risk for posttraumatic stress disorder (PTSD) depends on the number of traumatic event types experienced in a dose response relationship, but genetic factors are known to also influence the risk of PTSD. The catechol-O-methyltransferase (COMT) Val158Met polymorphism has been found to affect fear extinction and might play a role in the etiology of anxiety disorders.&lt;br /&gt;Methods&lt;br /&gt;Traumatic load and lifetime and current diagnosis of PTSD and COMT genotype were assessed in a sample of 424 survivors of the Rwandan Genocide living in the Nakivale refugee camp in southwestern Uganda.&lt;br /&gt;Results&lt;br /&gt;Higher numbers of different lifetime traumatic event types led to a higher prevalence of lifetime PTSD in a dose response relationship. However, this effect was modulated by the COMT genotype: whereas Val allele carriers showed the typical dose response relationship, Met/Met homozygotes exhibited a high risk for PTSD independently of the severity of traumatic load.&lt;br /&gt;Conclusions&lt;br /&gt;The present findings indicate a gene environment interaction between the human COMT Val158Met polymorphism and the number of traumatic event types experienced in the risk of developing PTSD.</dcterms:abstract>
    <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/43"/>
    <dcterms:bibliographicCitation>First publ. in: Biological Psychiatry ; 67 (2010), 4. - S. 304-308</dcterms:bibliographicCitation>
    <dc:contributor>Ertl, Verena</dc:contributor>
    <dc:date rdf:datatype="http://www.w3.org/2001/XMLSchema#dateTime">2011-03-25T09:20:16Z</dc:date>
    <dcterms:rights rdf:resource="https://rightsstatements.org/page/InC/1.0/"/>
    <void:sparqlEndpoint rdf:resource="http://localhost/fuseki/dspace/sparql"/>
    <dc:creator>Ertl, Verena</dc:creator>
    <dcterms:hasPart rdf:resource="https://kops.uni-konstanz.de/bitstream/123456789/10635/1/Kolassa_etal_2010_BiologicalPsychiatry.pdf"/>
    <dc:creator>Papassotiropoulos, Andreas</dc:creator>
    <bibo:uri rdf:resource="http://kops.uni-konstanz.de/handle/123456789/10635"/>
    <dc:contributor>Kolassa, Stephan</dc:contributor>
    <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/52"/>
    <dspace:isPartOfCollection rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/43"/>
    <dc:contributor>Kolassa, Iris-Tatjana</dc:contributor>
    <dc:creator>Quervain, Dominique J.-F. de</dc:creator>
    <dc:creator>Kolassa, Iris-Tatjana</dc:creator>
    <dcterms:isPartOf rdf:resource="https://kops.uni-konstanz.de/server/rdf/resource/123456789/52"/>
  </rdf:Description>
</rdf:RDF>
Interner Vermerk
xmlui.Submission.submit.DescribeStep.inputForms.label.kops_note_fromSubmitter
Kontakt
URL der Originalveröffentl.
Prüfdatum der URL
Prüfungsdatum der Dissertation
Finanzierungsart
Kommentar zur Publikation
Allianzlizenz
Corresponding Authors der Uni Konstanz vorhanden
Internationale Co-Autor:innen
Universitätsbibliographie
Ja
Begutachtet
Diese Publikation teilen