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

• Published in: Development and psychopathology 2013-08, Vol.25 (3), p.587-598
• Main Authors: Hayden, Elizabeth P, Olino, Thomas M, Bufferd, Sara J, Miller, Anna, Dougherty, Lea R, Sheikh, Haroon I, Singh, Shiva M, Klein, Daniel N
• Format: Article
• Language: English
• Subjects: Adult; Affect; Brain; Brain-derived neurotrophic factor; Brain-Derived Neurotrophic Factor - genetics; Child of Impaired Parents - psychology; Child, Preschool; Cognition & reasoning; Depressive Disorder - genetics; Depressive Disorder - psychology; Female; Genetic Predisposition to Disease; Genotype; Humans; Male; Memory; Mental depression; Middle Aged; Mothers - psychology; Neuropsychological Tests; Neuroses; Polymorphism; Polymorphism, Single Nucleotide; Psychiatric Status Rating Scales; Self Report; Serotonin; Serotonin Plasma Membrane Transport Proteins - genetics
• ISSN: 0954-5794; 1469-2198
• DOI: 10.1017/S0954579413000035

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.