ArticleDevelopment and psychopathology2013
The serotonin transporter linked polymorphic region and brain-derived neurotrophic factor valine to methionine at position 66 polymorphisms and maternal history of depression: associations with cognitive vulnerability to depression in childhood.
Article in Development and psychopathology, 2013. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Cited by 7 papers.
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Who cites it
7 citing papers in PubMed, 15 citations in OpenAlex.
- Long-Term Effects of Maternal Depression during Postpartum and Early Parenthood Period on Child Socioemotional Development.Children (Basel, Switzerland) · 2023Article
- Self-evaluation as an active ingredient in the experience and treatment of adolescent depression; an integrated scoping review with expert advisory input.BMC psychiatry · 2021Article
- The BDNF gene val66met polymorphism and behavioral inhibition in early childhood.Social development (Oxford, England) · 2018Article
- Mothers' Early Depressive Symptoms and Preschoolers' Behavioral Problems: The Moderating Role of Genetic Influences.Child psychiatry and human development · 2017Article
- Article
- Stability of self-referent encoding task performance and associations with change in depressive symptoms from early to middle childhood.Cognition & emotion · 2015Article
- Parental depression and child cognitive vulnerability predict children's cortisol reactivity.Development and psychopathology · 2014Article
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Authors and funding
8 authors at 2 institutions in 2 countries.
Funding
Abstract
Preliminary work indicates that cognitive vulnerability to depression may be associated with variants of the serotonin transporter promoter polymorphism (5-HTTLPR) and the valine to methionine at position 66 (val66met) polymorphism of the brain-derived neurotrophic factor (BDNF) gene; however, existing reports come from small samples. The present study sought to replicate and extend this research in a sample of 375 community-dwelling children and their parents. Following a negative mood induction, children completed a self-referent encoding task tapping memory for positive and negative self-descriptive traits. Consistent with previous work, we found that children with at least one short variant of the 5-HTTLPR had enhanced memory for negative self-descriptive traits. The BDNF val66met polymorphism had no main effect but was moderated by maternal depression, such that children with a BDNF methionine allele had a heightened memory for negative self-descriptive traits when mothers had experienced depression during children's lifetimes; in contrast, children with a methionine allele had low recall of negative traits when mothers had no depression history. The findings provide further support for the notion that the 5-HTTLPR is associated with cognitive markers of depression vulnerability and that the BDNF methionine allele moderates children's sensitivity to contextual factors.
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