Effects of the 2-Repeat Allele of the DRD4 Gene on Neural Networks Associated With the Prefrontal Cortex in Children With ADHD

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...

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Main Authors: Andan Qian, Jiejie Tao, Xin Wang, Huiru Liu, Lingxiao Ji, Chuang Yang, Qiong Ye, Chengchun Chen, Jiance Li, Jingliang Cheng, Meihao Wang, Ke Zhao
Format: Article
Language:English
Published: Frontiers Media S.A. 2018-07-01
Series:Frontiers in Human Neuroscience
Subjects:
Online Access:https://www.frontiersin.org/article/10.3389/fnhum.2018.00279/full
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spelling doaj-0f30ec7fe80347f0a5e0f301303ab0362020-11-25T03:00:56ZengFrontiers Media S.A.Frontiers in Human Neuroscience1662-51612018-07-011210.3389/fnhum.2018.00279335433Effects of the 2-Repeat Allele of the DRD4 Gene on Neural Networks Associated With the Prefrontal Cortex in Children With ADHDAndan Qian0Jiejie Tao1Xin Wang2Huiru Liu3Lingxiao Ji4Chuang Yang5Qiong Ye6Chengchun Chen7Jiance Li8Jingliang Cheng9Meihao Wang10Ke Zhao11Department of Radiology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ChinaDepartment of Radiology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ChinaDepartment of Radiology, Yancheng First Peoples’ Hospital, Yancheng, ChinaDepartment of Radiology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ChinaDepartment of Radiology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ChinaDepartment of Mental Health, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ChinaDepartment of Radiology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ChinaDepartment of Anatomy, Wenzhou Medical University, Wenzhou, ChinaDepartment of Radiology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ChinaDepartment of Radiology, First Affiliated Hospital of Zhengzhou University, Zhengzhou, ChinaDepartment of Radiology, First Affiliated Hospital of Wenzhou Medical University, Wenzhou, ChinaSchool of Mental Health, Wenzhou Medical University, Wenzhou, ChinaObjective: 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.https://www.frontiersin.org/article/10.3389/fnhum.2018.00279/fullattention-deficit hyperactivity disorderfunctional magnetic resonance imagingDRD42-repeat allelegroup independent component analysis
collection DOAJ
language English
format Article
sources DOAJ
author Andan Qian
Jiejie Tao
Xin Wang
Huiru Liu
Lingxiao Ji
Chuang Yang
Qiong Ye
Chengchun Chen
Jiance Li
Jingliang Cheng
Meihao Wang
Ke Zhao
spellingShingle Andan Qian
Jiejie Tao
Xin Wang
Huiru Liu
Lingxiao Ji
Chuang Yang
Qiong Ye
Chengchun Chen
Jiance Li
Jingliang Cheng
Meihao Wang
Ke Zhao
Effects of the 2-Repeat Allele of the DRD4 Gene on Neural Networks Associated With the Prefrontal Cortex in Children With ADHD
Frontiers in Human Neuroscience
attention-deficit hyperactivity disorder
functional magnetic resonance imaging
DRD4
2-repeat allele
group independent component analysis
author_facet Andan Qian
Jiejie Tao
Xin Wang
Huiru Liu
Lingxiao Ji
Chuang Yang
Qiong Ye
Chengchun Chen
Jiance Li
Jingliang Cheng
Meihao Wang
Ke Zhao
author_sort Andan Qian
title Effects of the 2-Repeat Allele of the DRD4 Gene on Neural Networks Associated With the Prefrontal Cortex in Children With ADHD
title_short Effects of the 2-Repeat Allele of the DRD4 Gene on Neural Networks Associated With the Prefrontal Cortex in Children With ADHD
title_full Effects of the 2-Repeat Allele of the DRD4 Gene on Neural Networks Associated With the Prefrontal Cortex in Children With ADHD
title_fullStr Effects of the 2-Repeat Allele of the DRD4 Gene on Neural Networks Associated With the Prefrontal Cortex in Children With ADHD
title_full_unstemmed Effects of the 2-Repeat Allele of the DRD4 Gene on Neural Networks Associated With the Prefrontal Cortex in Children With ADHD
title_sort effects of the 2-repeat allele of the drd4 gene on neural networks associated with the prefrontal cortex in children with adhd
publisher Frontiers Media S.A.
series Frontiers in Human Neuroscience
issn 1662-5161
publishDate 2018-07-01
description 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.
topic attention-deficit hyperactivity disorder
functional magnetic resonance imaging
DRD4
2-repeat allele
group independent component analysis
url https://www.frontiersin.org/article/10.3389/fnhum.2018.00279/full
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