The risk for depression conferred by stressful life events is modified by variation at the serotonin transporter 5HTTLPR genotype:: evidence from the Spanish PREDICT-Gene cohort

被引:98
作者
Cervilla, J. A.
Molina, E.
Rivera, M.
Torres-Gonzalez, F.
Bellon, J. A.
Moreno, B.
Luna, J. D.
Lorente, J. A.
Mayoral, F.
King, M.
Nazareth, I.
Gutierrez, B.
机构
[1] Univ Granada, Fac Med, Inst Neurosci, Dept Psychiat, Granada 18012, Spain
[2] Univ Granada, Fac Med, Dept Med Legal Toxicol & Psiquiatria, Granada, Spain
[3] Univ Granada, Inst Neurociencias, Granada, Spain
[4] Univ Malaga, Dept Prevent Med, Ctr Atenc Primaria EI Palo, Red Invest Atenc Primaria,redIAAP, E-29071 Malaga, Spain
[5] Fdn IMABIS, Malaga, Spain
[6] Univ Granada, Dept Bioestadist, Granada, Spain
[7] Hosp Carlos Haya, Malaga, Spain
[8] UCL, Royal Free & Univ Coll Med Sch, Dept Mental Hlth Sci, London, England
[9] UCL, Dept Primary Care & Populat Sci, London, England
[10] MRC Gen Practice Res Framework, London, England
基金
英国医学研究理事会;
关键词
serotonin transporter gene polymorphism; SLC6A4; gene-environment interaction; affective disorders; social stress; primary care;
D O I
10.1038/sj.mp.4001981
中图分类号
Q5 [生物化学]; Q7 [分子生物学];
学科分类号
071010 ; 081704 ;
摘要
We report results from the PREDICT-Gene case-control study nested in a prospective cohort designed to identify predictors of the onset of depression among adult primary-care attendees. We tested the potential gene-by-environment interaction between 5HTTLPR genotype at the serotonin transporter gene and previous exposure to threatening life events (TLEs) in depression. A total of 737 consecutively recruited participants were genotyped. Additional information was gathered on exposure to TLEs over a 6-month period, socio-demographic data and family history of psychological problems among first-degree relatives. Diagnoses of depression were ascertained using the Composite International Diagnostic Interview (CIDI) by trained interviewers. Two different depressive outcomes were used (ICD-10 depressive episode and ICD-10 severe depressive episode). Both the s/s genotype and exposure to increasing number of TLEs were significantly associated with depression. Moreover, the 5HTTLPR s/s genotype significantly modified the risk conferred by TLEs for both depressive outcomes. Thus, s/s homozygous participants required minimal exposure to TLE (11 TLE) to acquire a level of risk for depression that was only found among I/s or I/I individuals after significantly higher exposure to TLEs (two or more TLEs). The interaction was more apparent when applied to the diagnosis of ICD-10 severe depressive episode and after adjusting for gender, age and family history of psychological problems. Likelihood ratios tests for the interaction were statistically significant for both depressive outcomes (ICD-10 depressive episode: LR X-2=4.7, P=0.09 (crude), LR-X-2=6.4, P=0.04 (adjusted); ICD-10 severe depressive episode: LR X-2=6.9, P=0.032 (crude), LR-X-2=8.1, P=0.017 (adjusted)).
引用
收藏
页码:748 / 755
页数:8
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