Abstract

Objective: Genetic variation, especially polymorphism of the dopamine D4 receptor gene (DRD4), has been linked to deficits in self-regulation and executive functions and to attention deficit hyperactivity disorder (ADHD), and is related to the structural and functional integrity of the default mode network (DMN), the executive control network (ECN) and the sensorimotor network (SMN). The aim of this study was to explore the effects of the 2-repeat allele of the DRD4 gene on brain network connectivity and behaviors in children with ADHD.Methods: Using independent component analysis (ICA) and dimension analyses, we examined resting-state functional magnetic resonance imaging (fMRI) data obtained from 52 Asian medicine-naive children with ADHD (33 2-repeat absent and 19 2-repeat present).Results: We found that individuals with 2-repeat absent demonstrated increased within-network connectivity in the right precuneus of the DMN, the right middle frontal gyrus (MFG) of the SMN compared with individuals with 2-repeat present. Within the ECN, 2-repeat absent showed decreased within-network connectivity in the left inferior frontal gyrus (IFG) and the left anterior cingulate cortex. A deeper study found that connectivity strength of the left IFG was directly proportional to the Stroop reaction time in 2-repeat absent group, and as well as the right MFG in 2-repeat present group.Conclusion: Polymorphisms of the DRD4 gene, specifically 2-repeat allele, had effects on the ECN, the SMN and the DMN, especially in the prefrontal cortex (PFC) circles. ADHD children with DRD4 2-repeat allele have aberrant resting-state within-network connectivity patterns in the left IFG and the right MFG related to dysfunction in inattention symptom. This study provided novel insights into the neural mechanisms underlying the effects of DRD4 2-repeat allele on ADHD.

Highlights

  • Attention deficit hyperactivity disorder (ADHD) is a multifactorial, polygenetic disorder, characterized by inattention, impulsivity and hyperactivity, with a worldwide prevalence of 5.3% (Polanczyk et al, 2007)

  • As a higher score on the reaction time (RT) reflected poor performance, the higher levels of left inferior frontal gyrus (IFG) activity in 2-repeat absent group were associated with decreased performance-based levels of attention. These results suggested that 2-repeat alleles disturb the neuronal circuit of the left IFG and right middle frontal gyrus (MFG), which makes interference in the process of a high demand on selective attention test

  • Our study focused on DRD4 2-repeat allele influencing brain networks of individuals with ADHD, which has been rarely studied

Read more

Summary

Introduction

Attention deficit hyperactivity disorder (ADHD) is a multifactorial, polygenetic disorder, characterized by inattention, impulsivity and hyperactivity, with a worldwide prevalence of 5.3% (Polanczyk et al, 2007). ADHD is associated with neuropsychological deficits, academic difficulties and behavior problems that lead to social and mental issues (Able et al, 2007; Lingam et al, 2012). The leading candidate gene was dopamine D4 receptor gene (DRD4), which is the strongest and most consistently replicated gene related to ADHD (Banaschewski et al, 2010). A frequently studied polymorphism of the DRD4 gene is a 48 base-pair (bp) variable number of tandem repeats (VNTR) located on exon III. Molecular genetic studies showed that the DRD4 gene regulates the efficiency of the central dopaminergic pathways. In comparison with 4-repeat alleles, 7-repeat alleles exhibited a suboptimal response to dopamine, whereas 2-repeat alleles exhibited an intermediate profile (Asghari et al, 1995; Oak et al, 2000)

Methods
Results
Conclusion

Talk to us

Join us for a 30 min session where you can share your feedback and ask us any queries you have

Schedule a call

Disclaimer: All third-party content on this website/platform is and will remain the property of their respective owners and is provided on "as is" basis without any warranties, express or implied. Use of third-party content does not indicate any affiliation, sponsorship with or endorsement by them. Any references to third-party content is to identify the corresponding services and shall be considered fair use under The CopyrightLaw.