Abstract
Background: There is inconsistent evidence of interaction between stressful events and a serotonin transporter promoter polymorphism (5-HTTLPR) in depression. Recent studies have indicated that the moderating effect of 5-HTTLPR may be strongest when adverse experiences have occurred in childhood and the depressive symptoms persist over time. However, it is unknown whether this gene-environment interaction is present for recurrent depressive disorder and different forms of maltreatment. Therefore, patients with recurrent clinically diagnosed depression and controls screened for the absence of depression were utilised to examine the moderating effect of 5-HTTLPR on associations between specific forms of childhood adversity and recurrent depression. Method: A sample of 227 recurrent unipolar depression cases and 228 never psychiatrically ill controls completed the Childhood Trauma Questionnaire to assess exposure to sexual, physical and emotional abuse, physical and emotional neglect in childhood. DNA extracted from blood or cheek swabs was genotyped for the short (s) and long (l) alleles of 5-HTTLPR. Results: All forms of childhood maltreatment were reported as more severe by cases than controls. There was no direct association between 5-HTTLPR and depression. Significant interactions with additive and recessive 5-HTTLPR genetic models were found for overall severity of maltreatment, sexual abuse and to a lesser degree for physical neglect, but not other maltreatment types. Limitations: The cross-sectional design limits causal inference. Retrospective report of childhood adversity may have reduced the accuracy of the findings. Conclusions: This study provides support for the role of interplay between 5-HTTLPR and a specific early environmental risk in recurrent depressive disorder.
Original language | English |
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Pages (from-to) | 136-141 |
Number of pages | 6 |
Journal | Journal of Affective Disorders |
Volume | 145 |
Issue number | 1 |
DOIs | |
Publication status | Published - Feb 15 2013 |
Externally published | Yes |
Bibliographical note
Funding Information:Funding for the DeCC study was provided by the UK Medical Research Council (MRC). Helen L. Fisher was funded by an MRC Population Health Scientist award (G1002366). Georgina M. Hosang was supported an MRC and Economic and Social Research Council (ESRC) interdisciplinary postdoctoral fellowship. Sarah Cohen-Woods was funded by a postdoctoral fellowship from the National Institute for Health Research (NIHR) Specialist Biomedical Research Centre for Mental Health at the South London and Maudsley NHS Foundation Trust and the Institute of Psychiatry, King's College London. The funding organisations had no further role in study design; in the collection, analysis and interpretation of data; in the writing of the report; and in the decision to submit the paper for publication.
ASJC Scopus Subject Areas
- Clinical Psychology
- Psychiatry and Mental health