Collaborative meta-analysis finds no evidence of a strong interaction between stress and 5-HTTLPR genotype contributing to the development of depression

被引:0
|
作者
R C Culverhouse
N L Saccone
A C Horton
Y Ma
K J Anstey
T Banaschewski
M Burmeister
S Cohen-Woods
B Etain
H L Fisher
N Goldman
S Guillaume
J Horwood
G Juhasz
K J Lester
L Mandelli
C M Middeldorp
E Olié
S Villafuerte
T M Air
R Araya
L Bowes
R Burns
E M Byrne
C Coffey
W L Coventry
K A B Gawronski
D Glei
A Hatzimanolis
J-J Hottenga
I Jaussent
C Jawahar
C Jennen-Steinmetz
J R Kramer
M Lajnef
K Little
H M zu Schwabedissen
M Nauck
E Nederhof
P Petschner
W J Peyrot
C Schwahn
G Sinnamon
D Stacey
Y Tian
C Toben
S Van der Auwera
N Wainwright
J-C Wang
G Willemsen
机构
[1] Washington University in St. Louis School of Medicine,Department of Medicine and Division of Biostatistics
[2] Washington University in St. Louis School of Medicine,Department of Genetics and Division of Biostatistics
[3] Washington University in St. Louis School of Medicine,Department of Psychiatry
[4] Centre for Research on Ageing,Department of Child and Adolescent Psychiatry and Psychotherapy
[5] Health and Wellbeing,Department of Psychiatry
[6] The Australian National University,Department of Human Genetics
[7] Central Institute of Mental Health,Department of Emergency Psychiatry and Acute Care
[8] Medical Faculty Mannheim/Heidelberg University,Department of Psychological Medicine
[9] University of Michigan,Department of Pharmacodynamics
[10] University of Michigan,Department of Biomedical and NeuroMotor Sciences
[11] School of Psychology,Department of Biological Psychology
[12] Faculty of Social and Behavioural Sciences,Department of Experimental Psychology
[13] Flinders University,Department of Genetics
[14] Sorbonne Paris Cité,Department of Psychiatry
[15] Université Paris Diderot,Department of Biostatistics
[16] UMR-S 1144,Department of Psychiatry
[17] AP-HP,Department of Paediatrics and School of Psychological Sciences
[18] Groupe Saint-Louis-Lariboisière-F. Widal,Department Pharmaceutical Sciences
[19] INSERM,Department of Psychiatry
[20] U1144,Department of Prosthetic Dentistry
[21] Social,Department of Epidemiology and Biostatistics
[22] Genetic & Developmental Psychiatry Centre,Department of Psychiatry and Psychotherapy
[23] Institute of Psychiatry,Department of Public Health and Primary Care
[24] Psychology & Neuroscience,Department of Neuroscience
[25] King's College London,Department of Psychiatry and Psychotherapy
[26] Office of Population Research,Department of Psychiatry and Psychotherapy
[27] Princeton University,Fellow Program and Behavioral Health and Criminal Justice Division
[28] Université Montpellier,Department of Pathology
[29] INSERM U1061 Neuropsychiatry,Department of Paediatrics and School of Psychological Sciences
[30] CHU Montpellier,Department of Paediatrics
[31] University of Otago Christchurch,Department of Health Sciences
[32] MTA-SE-NAP B Genetic Brain Imaging Migraine Research Group,Department of Psychiatry
[33] Hungarian Academy of Sciences,Departments of Psychiatry and Medical and Molecular Genetics
[34] Semmelweis University,undefined
[35] Semmelweis University,undefined
[36] Neuroscience and Psychiatry Unit,undefined
[37] The University of Manchester,undefined
[38] NAP-A-SE New Antidepressant Target Research Group,undefined
[39] Semmelweis University,undefined
[40] School of Psychology,undefined
[41] University of Sussex,undefined
[42] University of Bologna,undefined
[43] Vrije Universiteit Amsterdam,undefined
[44] Neuroscience Campus Amsterdam,undefined
[45] Vrije Universiteit Amsterdam,undefined
[46] Discipline of Psychiatry,undefined
[47] University of Adelaide,undefined
[48] Centre for Global Mental Health,undefined
[49] London School of Hygiene and Tropical Medicine,undefined
[50] University of Oxford,undefined
来源
Molecular Psychiatry | 2018年 / 23卷
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摘要
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.
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页码:133 / 142
页数:9
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