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Default mode network connectivity and social dysfunction in children with Attention Deficit/Hyperactivity Disorder

OBJECTIVE: Attention Deficit/Hyperactivity Disorder (ADHD) negatively affects social functioning; however, its neurological underpinnings remain unclear. Altered Default Mode Network (DMN) connectivity may contribute to social dysfunction in ADHD. We investigated whether DMN's dynamic functiona...

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Autores principales: Fateh, Ahmed Ameen, Huang, Wenxian, Hassan, Muhammad, Zhuang, Yijiang, Lin, Jieqiong, Luo, Yi, Yang, Binrang, Zeng, Hongwu
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Asociacion Espanola de Psicologia Conductual 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564936/
https://www.ncbi.nlm.nih.gov/pubmed/37829190
http://dx.doi.org/10.1016/j.ijchp.2023.100393
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author Fateh, Ahmed Ameen
Huang, Wenxian
Hassan, Muhammad
Zhuang, Yijiang
Lin, Jieqiong
Luo, Yi
Yang, Binrang
Zeng, Hongwu
author_facet Fateh, Ahmed Ameen
Huang, Wenxian
Hassan, Muhammad
Zhuang, Yijiang
Lin, Jieqiong
Luo, Yi
Yang, Binrang
Zeng, Hongwu
author_sort Fateh, Ahmed Ameen
collection PubMed
description OBJECTIVE: Attention Deficit/Hyperactivity Disorder (ADHD) negatively affects social functioning; however, its neurological underpinnings remain unclear. Altered Default Mode Network (DMN) connectivity may contribute to social dysfunction in ADHD. We investigated whether DMN's dynamic functional connectivity (dFC) alterations were associated with social dysfunction in individuals with ADHD. METHODS: Resting-state fMRI was used to examine DMN subsystems (dorsal medial prefrontal cortex (dMPFC), medial temporal lobe (MTL)) and the midline core in 40 male ADHD patients (7-10 years) and 45 healthy controls (HCs). Connectivity correlations with symptoms and demographic data were assessed. Group-based analyses compared rsFC between groups with two-sample t-tests and post-hoc analyses. RESULTS: Social dysfunction in ADHD patients was related to reduced DMN connectivity, specifically in the MTL subsystem and the midline core. ADHD patients showed decreased dFC between parahippocampal cortex (PHC) and left superior frontal gyrus, and between ventral medial prefrontal cortex (vMPFC) and right middle frontal gyrus compared to HCs (MTL subsystem). Additionally, decreased dFC between posterior cingulate cortex (PCC), anterior medial prefrontal cortex (aMPFC), and right angular gyrus (midline core) was observed in ADHD patients relative to HCs. No abnormal connectivity was found within the dMPFC. CONCLUSION: Preliminary findings suggest that DMN connectional abnormalities may contribute to social dysfunction in ADHD, providing insights into the disorder's neurobiology and pathophysiology.
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spelling pubmed-105649362023-10-12 Default mode network connectivity and social dysfunction in children with Attention Deficit/Hyperactivity Disorder Fateh, Ahmed Ameen Huang, Wenxian Hassan, Muhammad Zhuang, Yijiang Lin, Jieqiong Luo, Yi Yang, Binrang Zeng, Hongwu Int J Clin Health Psychol Original Article OBJECTIVE: Attention Deficit/Hyperactivity Disorder (ADHD) negatively affects social functioning; however, its neurological underpinnings remain unclear. Altered Default Mode Network (DMN) connectivity may contribute to social dysfunction in ADHD. We investigated whether DMN's dynamic functional connectivity (dFC) alterations were associated with social dysfunction in individuals with ADHD. METHODS: Resting-state fMRI was used to examine DMN subsystems (dorsal medial prefrontal cortex (dMPFC), medial temporal lobe (MTL)) and the midline core in 40 male ADHD patients (7-10 years) and 45 healthy controls (HCs). Connectivity correlations with symptoms and demographic data were assessed. Group-based analyses compared rsFC between groups with two-sample t-tests and post-hoc analyses. RESULTS: Social dysfunction in ADHD patients was related to reduced DMN connectivity, specifically in the MTL subsystem and the midline core. ADHD patients showed decreased dFC between parahippocampal cortex (PHC) and left superior frontal gyrus, and between ventral medial prefrontal cortex (vMPFC) and right middle frontal gyrus compared to HCs (MTL subsystem). Additionally, decreased dFC between posterior cingulate cortex (PCC), anterior medial prefrontal cortex (aMPFC), and right angular gyrus (midline core) was observed in ADHD patients relative to HCs. No abnormal connectivity was found within the dMPFC. CONCLUSION: Preliminary findings suggest that DMN connectional abnormalities may contribute to social dysfunction in ADHD, providing insights into the disorder's neurobiology and pathophysiology. Asociacion Espanola de Psicologia Conductual 2023 2023-07-04 /pmc/articles/PMC10564936/ /pubmed/37829190 http://dx.doi.org/10.1016/j.ijchp.2023.100393 Text en © 2023 The Author(s) https://creativecommons.org/licenses/by-nc-nd/4.0/This is an open access article under the CC BY-NC-ND license (http://creativecommons.org/licenses/by-nc-nd/4.0/).
spellingShingle Original Article
Fateh, Ahmed Ameen
Huang, Wenxian
Hassan, Muhammad
Zhuang, Yijiang
Lin, Jieqiong
Luo, Yi
Yang, Binrang
Zeng, Hongwu
Default mode network connectivity and social dysfunction in children with Attention Deficit/Hyperactivity Disorder
title Default mode network connectivity and social dysfunction in children with Attention Deficit/Hyperactivity Disorder
title_full Default mode network connectivity and social dysfunction in children with Attention Deficit/Hyperactivity Disorder
title_fullStr Default mode network connectivity and social dysfunction in children with Attention Deficit/Hyperactivity Disorder
title_full_unstemmed Default mode network connectivity and social dysfunction in children with Attention Deficit/Hyperactivity Disorder
title_short Default mode network connectivity and social dysfunction in children with Attention Deficit/Hyperactivity Disorder
title_sort default mode network connectivity and social dysfunction in children with attention deficit/hyperactivity disorder
topic Original Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10564936/
https://www.ncbi.nlm.nih.gov/pubmed/37829190
http://dx.doi.org/10.1016/j.ijchp.2023.100393
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