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Additive gene-environment effects on hippocampal structure in healthy humans.
Rabl, Ulrich; Meyer, Bernhard M; Diers, Kersten; Bartova, Lucie; Berger, Andreas; Mandorfer, Dominik; Popovic, Ana; Scharinger, Christian; Huemer, Julia; Kalcher, Klaudius; Pail, Gerald; Haslacher, Helmuth; Perkmann, Thomas; Windischberger, Christian; Brocke, Burkhard; Sitte, Harald H; Pollak, Daniela D; Dreher, Jean-Claude; Kasper, Siegfried; Praschak-Rieder, Nicole; Moser, Ewald; Esterbauer, Harald; Pezawas, Lukas.
Afiliação
  • Rabl U; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Meyer BM; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Diers K; Department of Psychology, Dresden University of Technology, 01069 Dresden, Germany.
  • Bartova L; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Berger A; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Mandorfer D; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Popovic A; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Scharinger C; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Huemer J; Department of Child and Adolescent Psychiatry.
  • Kalcher K; MR Center of Excellence, Center for Medical Physics and Biomedical Engineering.
  • Pail G; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Haslacher H; Department of Laboratory Medicine.
  • Perkmann T; Department of Laboratory Medicine.
  • Windischberger C; MR Center of Excellence, Center for Medical Physics and Biomedical Engineering.
  • Brocke B; Department of Psychology, Dresden University of Technology, 01069 Dresden, Germany.
  • Sitte HH; Center of Physiology and Pharmacology, Institute of Pharmacology, and.
  • Pollak DD; Department of Neurophysiology and Neuropharmacology, Center for Physiology and Pharmacology, Medical University of Vienna, A-1090 Vienna, Austria.
  • Dreher JC; Neuroeconomics Laboratory: Reward and Decision-Making, Centre de Neurosciences Cognitives, Centre National de la Recherche Scientifique/Unité Mixte de Recherche 5229, 69500 Bron, France, and Université Claude Bernard Lyon 1, 69100 Villeurbanne, France.
  • Kasper S; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Praschak-Rieder N; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria.
  • Moser E; MR Center of Excellence, Center for Medical Physics and Biomedical Engineering.
  • Esterbauer H; Department of Laboratory Medicine.
  • Pezawas L; Department of Psychiatry and Psychotherapy, Medical University of Vienna, A-1090 Vienna, Austria, lukas.pezawas@meduniwien.ac.at.
J Neurosci ; 34(30): 9917-26, 2014 Jul 23.
Article em En | MEDLINE | ID: mdl-25057194
ABSTRACT
Hippocampal volume loss has been related to chronic stress as well as genetic factors. Although genetic and environmental variables affecting hippocampal volume have extensively been studied and related to mental illness, limited evidence is available with respect to G × E interactions on hippocampal volume. The present MRI study investigated interaction effects on hippocampal volume between three well-studied functional genetic variants (COMT Val158Met, BDNF Val66Met, 5-HTTLPR) associated with hippocampal volume and a measure of environmental adversity (life events questionnaire) in a large sample of healthy humans (n = 153). All three variants showed significant interactions with environmental adversity with respect to hippocampal volume. Observed effects were additive by nature and driven by both recent as well as early life events. A consecutive analysis of hippocampal subfields revealed a spatially distinct profile for each genetic variant suggesting a specific role of 5-HTTLPR for the subiculum, BDNF Val66Met for CA4/dentate gyrus, and COMT Val158Met for CA2/3 volume changes. The present study underscores the importance of G × E interactions as determinants of hippocampal volume, which is crucial for the neurobiological understanding of stress-related conditions, such as mood disorders or post-traumatic stress disorder (PTSD).
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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nível de Saúde / Interação Gene-Ambiente / Hipocampo / Acontecimentos que Mudam a Vida Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Assunto principal: Nível de Saúde / Interação Gene-Ambiente / Hipocampo / Acontecimentos que Mudam a Vida Limite: Adolescent / Adult / Female / Humans / Male Idioma: En Ano de publicação: 2014 Tipo de documento: Article