Abstract

Parental psychopathological risk is considered as one of the most crucial features associated with epigenetic modifications in offspring, which in turn are thought to be related to their emotional/behavioral profiles. The dopamine active transporter (DAT) gene is suggested to play a significant role in affective/behavioral regulation. On the basis of the previous literature, we aimed at verifying whether children’s DAT1 polymorphisms moderated the relationship between parents’ psychological profiles, children’s emotional/behavioral functioning, and DAT1 methylation in a normative sample of 79 families with school-age children (Ntot = 237). Children’s biological samples were collected through buccal swabs, while Symptom Check-List-90 item Revised, Adult Self Report, and Child Behavior Check-List/6–18 was administered to assess parental and children’s psychological functioning. We found that higher maternal externalizing problems predicted the following: higher levels of children’s DAT1 methylation at M1, but only among children with 10/10 genotype; higher levels of methylation at M2 among children with 10/10 genotype; while lower levels for children with a 9-repeat allele. There was also a positive relationship between fathers’ externalizing problems and children’s externalizing problems, only for children with a 9-repeat allele. Our findings support emerging evidence of the complex interplay between genetic and environmental factors in shaping children’ emotional/behavioral functioning, contributing to the knowledge of risk variables for a child’s development and psychological well-being.

Highlights

  • In recent decades, a growing amount of research has underlined the complex interplay between genes and the environment in shaping children’s development and emotional/behavioral adaptive functioning [1,2,3].Int

  • We included interaction terms between children’s genotype and all parental psychological variables considered in step 1

  • For children’s methylation of dopamine active transporter 1 (DAT1) gene at CpG M1, the results showed no significant predictors at the first step, but in step 2, it was predicted by the father’s externalizing problems (β = 1.02; t = 3.14; p = 0.003) and by the interaction between children’s DAT1 genotype and maternal externalizing problems (β = 0.54; t = 2.93; p = 0.006)

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Summary

Methods

Thanks to the collaboration with primary schools of Central Italy, we recruited 117 families (composed of mothers, fathers, and one child) with children aged from 6 to 11 years old. The final sample was composed of 79 children (43 females and 36 males with age ranging from 6 to 11 years; M = 7.78 years; SD = 1.57), their mothers (M = 41.53 years; SD = 4.86), and their fathers (M = 43.83 years, SD = 5.10). The families were 100% Caucasian, and most of the families (88.61%). A large majority (97.47%) of families were intact family groups. 86.07% of children were first-born for both parents

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