Disordered eating in early childhood: DRD4 and DAT1 gene polymorphisms and quality of mother-child interaction

Eat Weight Disord. 2022 Oct;27(7):2605-2616. doi: 10.1007/s40519-022-01408-4. Epub 2022 May 5.

Abstract

Purpose: Eating disturbances are complex heritable conditions that can be influenced by both genetic and environmental factors but are poorly studied in early development. The aim of this research was to investigate the association of genetic polymorphisms within dopaminergic pathways with early feeding problems.

Methods: We analyzed the presence of VNTR polymorphisms of DRD4 (rs1805186) and DAT1 (rs28363170) in overeating (N = 45), undereating (N = 48) and control (N = 44) young children. We also assessed presence of externalizing, internalizing and dysregulation symptoms by the Child Behavior Checklist and quality of mother-child interactions during feeding by the Italian adaptation of the Scale for the Assessment of Feeding Interaction, respectively.

Results: Both polymorphisms were associated with children's eating behavior, psychological symptoms and quality of interaction with their mothers, suggesting that: (a) the DRD4 4-repeat allele behaves as a protective factor, the 2-repeats and 7-repeats alleles as risk factors, for undereating behavior, the general quality of mother-child interaction and internalizing, externalizing and dysregulated symptoms; and (b) the DAT1 9-repeats allele behaves as a protective factor, the 10-repeats allele as a risk factor, for overeating behavior, the general quality of mother-child interaction, internalizing, externalizing and dysregulated symptoms. Finally, a gene x gene interaction is suggested between the DAT1 9-repeat or 10-repeat allele and the DRD4 4-repeat allele.

Conclusions: Our results suggest a role for DRD4 and DAT1 in an early susceptibility to eating disturbances.

Level of evidence iii: Evidence obtained from well-designed case-control analytic study.

Keywords: Children; DAT1 rs28363170; DRD4 rs1805186; Eating disturbances; Parent–child interaction.

MeSH terms

  • Alleles
  • Child, Preschool
  • Dopamine Plasma Membrane Transport Proteins / genetics*
  • Feeding and Eating Disorders*
  • Female
  • Genetic Predisposition to Disease
  • Genotype
  • Humans
  • Hyperphagia
  • Mother-Child Relations
  • Polymorphism, Genetic
  • Receptors, Dopamine D4* / genetics

Substances

  • DRD4 protein, human
  • Dopamine Plasma Membrane Transport Proteins
  • SLC6A3 protein, human
  • Receptors, Dopamine D4