Early Family Environment, Current Adversity, the Serotonin Transporter Promoter Polymorphism, and Depressive Symptomatology
Abstract
Background Mixed evidence has suggested that homozygous carriers of the short allele (s/s) of the serotonin transporter gene-linked polymorphic region (5-HTTLPR) may be at increased risk for depression, if they have also been exposed to early or current adversity/stress. We address this debate by examining the relation of a stressful early family environment, recent adversity/stress, and the 5-HTTLPR to depressive symptomatology in a normal sample.Methods A nonclinical sample of 118 young adult men and women completed assessments of early family environment, recent stressful events, psychosocial resources, and psychological distress, including depressive symptomatology. The 5-HTTLPR was genotyped using a standard protocol with DNA extracted from oral fluid.Results A stressful early family environment was significantly related to depressive symptomatology. In addition, gene-by-environment (GxE) interactions were observed between the 5-HTTLPR and both early family environment and current adversity/stress. Individuals homozygous for the short allele had greater depressive symptomatology if they had experienced early or recent adversity but significantly less depressive symptomatology if they reported a supportive early environment or recent positive experiences, compared with participants with the s/l or l/l genotype.Conclusions Early or current environment, in conjunction with the serotonin transporter polymorphism, predicts depressive symptomatology.
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Adverse early childhood conditions exacerbate the genetic liability of a polymorphism in the 5-HTT serotonin transporter gene, resulting in heightened risks for depression.
“Adverse early childhood conditions have also been shown to exacerbate the genetic liability of a polymorphism in the 5-HTT serotonin transporter gene, resulting in heightened risks for depression.133,198”
From Socio‐economic differentials in peripheral biology: Cumulative allostatic load (2010) · cites this paper as [198]
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References 28 · Cited by 432
- Authors
- Taylor, S. E., Way, B. M., Welch, W. T., Hilmert, C. J., Lehman, B. J., & Eisenberger, N. I.
- Affiliations
- University of California, Los Angeles (US)
- Corresponding author
- Taylor, Shelley E.
- Venue
- Biological Psychiatry
- Publisher
- Elsevier BV
- Published
- 2006-10
- Volume
- 60
- Issue
- 7
- Pages
- 671-676
- ISSN
- 0006-3223 (ISSN-L)
- OpenAlex
- W2170846744
- Cited by
- 432
- References
- 28
- Citations by year
- 2026: 3 · 2025: 3 · 2024: 7 · 2023: 10 · 2022: 14 · 2021: 12 · 2020: 10 · 2019: 19 · 2018: 8 · 2017: 18 · 2016: 26 · 2015: 33 · 2014: 28 · 2013: 37 · 2012: 35
- FWCI
- 9.98
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- Biological Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Funders
- University of California, Los Angeles (MH56880)
- National Science Foundation (BCS-0338631)
- National Institute of Mental Health (MH15750)
- Topics
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Life Sciences › Biochemistry, Genetics and Molecular Biology › Genetics › Genetic Associations and Epidemiology
- Life Sciences › Neuroscience › Behavioral Neuroscience › Stress Responses and Cortisol
- Keywords
- serotonin transporter gene, 5-HTTLPR, short allele, depressive symptoms, childhood adversity, gene-environment interaction, life events, psychosocial resources, psychological distress, young adults
- MeSH terms
- Adolescent, Adult, Age Factors, Depressive Disorder, Family Relations, Female, Humans, Male, Polymorphism, Genetic, Social Environment, Stress, Psychological, Time Factors, Genetic Predisposition to Disease, Serotonin Plasma Membrane Transport Proteins
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