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Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression.
Culverhouse, R C; Saccone, N L; Horton, A C; Ma, Y; Anstey, K J; Banaschewski, T; Burmeister, M; Cohen-Woods, S; Etain, B; Fisher, H L; Goldman, N; Guillaume, S; Horwood, J; Juhasz, G; Lester, K J; Mandelli, L; Middeldorp, C M; Olié, E; Villafuerte, S; Air, T M; Araya, R; Bowes, L; Burns, R; Byrne, E M; Coffey, C; Coventry, W L; Gawronski, K A B; Glei, D; Hatzimanolis, A; Hottenga, J-J; Jaussent, I; Jawahar, C; Jennen-Steinmetz, C; Kramer, J R; Lajnef, M; Little, K; Zu Schwabedissen, H M; Nauck, M; Nederhof, E; Petschner, P; Peyrot, W J; Schwahn, C; Sinnamon, G; Stacey, D; Tian, Y; Toben, C; Van der Auwera, S; Wainwright, N; Wang, J-C; Willemsen, G.
Affiliation
  • Culverhouse RC; Department of Medicine and Division of Biostatistics, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
  • Saccone NL; Department of Genetics and Division of Biostatistics, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
  • Horton AC; Department of Psychiatry, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
  • Ma Y; Department of Psychiatry, Washington University in St. Louis School of Medicine, St. Louis, MO, USA.
  • Anstey KJ; Centre for Research on Ageing, Health and Wellbeing, The Australian National University, Canberra, ACT, Australia.
  • Banaschewski T; Department of Child and Adolescent Psychiatry and Psychotherapy, Central Institute of Mental Health, Medical Faculty Mannheim/Heidelberg University, Mannheim, Germany.
  • Burmeister M; Department of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
  • Cohen-Woods S; Department of Human Genetics, University of Michigan, Ann Arbor, MI, USA.
  • Etain B; School of Psychology, Faculty of Social and Behavioural Sciences, Flinders University, Adelaide, SA, Australia.
  • Fisher HL; Sorbonne Paris Cité, Université Paris Diderot, UMR-S 1144, Paris, France.
  • Goldman N; AP-HP, Groupe Saint-Louis-Lariboisière-F. Widal, Paris, France.
  • Guillaume S; INSERM, U1144, Paris, France.
  • Horwood J; Social, Genetic & Developmental Psychiatry Centre, Institute of Psychiatry, Psychology & Neuroscience, King's College London, London, UK.
  • Juhasz G; Office of Population Research, Princeton University, Princeton, NJ, USA.
  • Lester KJ; Université Montpellier, Montpellier, France.
  • Mandelli L; INSERM U1061 Neuropsychiatry, Montpellier, France.
  • Middeldorp CM; Department of Emergency Psychiatry and Acute Care, CHU Montpellier, Montpellier, France.
  • Olié E; Department of Psychological Medicine, University of Otago Christchurch, Christchurch, New Zealand.
  • Villafuerte S; MTA-SE-NAP B Genetic Brain Imaging Migraine Research Group, Hungarian Academy of Sciences, Semmelweis University, Budapest, Hungary.
  • Air TM; Department of Pharmacodynamics, Semmelweis University, Budapest, Hungary.
  • Araya R; Neuroscience and Psychiatry Unit, The University of Manchester, Manchester, UK.
  • Bowes L; NAP-A-SE New Antidepressant Target Research Group, Semmelweis University, Budapest, Hungary.
  • Burns R; School of Psychology, University of Sussex, Brighton, UK.
  • Byrne EM; Department of Biomedical and NeuroMotor Sciences, University of Bologna, Bologna, Italy.
  • Coffey C; Department of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Coventry WL; Neuroscience Campus Amsterdam, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Gawronski KAB; Université Montpellier, Montpellier, France.
  • Glei D; INSERM U1061 Neuropsychiatry, Montpellier, France.
  • Hatzimanolis A; Department of Emergency Psychiatry and Acute Care, CHU Montpellier, Montpellier, France.
  • Hottenga JJ; Department of Psychiatry, University of Michigan, Ann Arbor, MI, USA.
  • Jaussent I; Discipline of Psychiatry, University of Adelaide, Adelaide, SA, Australia.
  • Jawahar C; Centre for Global Mental Health, London School of Hygiene and Tropical Medicine, London, UK.
  • Jennen-Steinmetz C; Department of Experimental Psychology, University of Oxford, Oxford, UK.
  • Kramer JR; Centre for Research on Ageing, Health and Wellbeing, The Australian National University, Canberra, ACT, Australia.
  • Lajnef M; Institute for Molecular Bioscience, University of Queensland, Brisbane, QLD, Australia.
  • Little K; Centre for Adolescent Health, Murdoch Childrens Research Institute, Melbourne, VIC, Australia.
  • Zu Schwabedissen HM; Discipline of Psychology, University of New England, Armidale, NSW, Australia.
  • Nauck M; Department of Genetics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, PA, USA.
  • Nederhof E; Center for Population and Health, Georgetown University, Washington, DC, USA.
  • Petschner P; Department of Psychiatry, Eginition Hospital, School of Medicine, National and Kapodistrian University of Athens, Athens, Greece.
  • Peyrot WJ; Neurobiology Research Institute, Theodor-Theohari Cozzika Foundation, Athens, Greece.
  • Schwahn C; Department of Biological Psychology, Vrije Universiteit Amsterdam, Amsterdam, The Netherlands.
  • Sinnamon G; EMGO+ Institute for Health and Care Research, VU Medical Center Amsterdam, Amsterdam, The Netherlands.
  • Stacey D; INSERM U1061 Neuropsychiatry, Montpellier, France.
  • Tian Y; Discipline of Psychiatry, University of Adelaide, Adelaide, SA, Australia.
  • Toben C; Department of Biostatistics, Central Institute of Mental Health, Medical Faculty Mannheim/Heidelberg University, Mannheim, Germany.
  • Van der Auwera S; Department of Psychiatry, Carver College of Medicine, University of Iowa, Iowa City, IA, USA.
  • Wainwright N; INSERM U955, Creteil, France.
  • Wang JC; Murdoch Childrens Research Institute, Melbourne, VIC, Australia.
  • Willemsen G; Department of Paediatrics and School of Psychological Sciences, University of Melbourne, Melbourne, VIC, Australia.
Mol Psychiatry ; 23(1): 133-142, 2018 01.
Article in En | MEDLINE | ID: mdl-28373689
ABSTRACT
The hypothesis that the S allele of the 5-HTTLPR serotonin transporter promoter region is associated with increased risk of depression, but only in individuals exposed to stressful situations, has generated much interest, research and controversy since first proposed in 2003. Multiple meta-analyses combining results from heterogeneous analyses have not settled the issue. To determine the magnitude of the interaction and the conditions under which it might be observed, we performed new analyses on 31 data sets containing 38 802 European ancestry subjects genotyped for 5-HTTLPR and assessed for depression and childhood maltreatment or other stressful life events, and meta-analysed the results. Analyses targeted two stressors (narrow, broad) and two depression outcomes (current, lifetime). All groups that published on this topic prior to the initiation of our study and met the assessment and sample size criteria were invited to participate. Additional groups, identified by consortium members or self-identified in response to our protocol (published prior to the start of analysis) with qualifying unpublished data, were also invited to participate. A uniform data analysis script implementing the protocol was executed by each of the consortium members. Our findings do not support the interaction hypothesis. We found no subgroups or variable definitions for which an interaction between stress and 5-HTTLPR genotype was statistically significant. In contrast, our findings for the main effects of life stressors (strong risk factor) and 5-HTTLPR genotype (no impact on risk) are strikingly consistent across our contributing studies, the original study reporting the interaction and subsequent meta-analyses. Our conclusion is that if an interaction exists in which the S allele of 5-HTTLPR increases risk of depression only in stressed individuals, then it is not broadly generalisable, but must be of modest effect size and only observable in limited situations.
Subject(s)

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stress, Psychological / Depression / Serotonin Plasma Membrane Transport Proteins Type of study: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Mol Psychiatry Journal subject: BIOLOGIA MOLECULAR / PSIQUIATRIA Year: 2018 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Stress, Psychological / Depression / Serotonin Plasma Membrane Transport Proteins Type of study: Prognostic_studies / Risk_factors_studies / Systematic_reviews Limits: Humans Language: En Journal: Mol Psychiatry Journal subject: BIOLOGIA MOLECULAR / PSIQUIATRIA Year: 2018 Type: Article Affiliation country: United States