| Literature DB >> 31322305 |
Clara Pretus1,2, Luis Marcos-Vidal3,4, Magdalena Martínez-García3, Marisol Picado1, Josep Antoni Ramos-Quiroga5,6,7, Vanesa Richarte5,6,7, Francisco X Castellanos8,9, Jorge Sepulcre10,11, Manuel Desco3,12,4,13, Óscar Vilarroya1,2, Susanna Carmona3,12,4.
Abstract
Neuroimaging studies indicate that children with attention-deficit/hyperactivity disorder (ADHD) present alterations in several functional networks of the sensation-to-cognition spectrum. These alterations include functional overconnectivity within sensory regions and underconnectivity between sensory regions and neural hubs supporting higher order cognitive functions. Today, it is unknown whether this same pattern of alterations persists in adult patients with ADHD who had never been medicated for their condition. The aim of the present study was to assess whether medication-naïve adults with ADHD presented alterations in functional networks of the sensation-to-cognition spectrum. Thirty-one medication-naïve adults with ADHD and twenty-two healthy adults underwent resting-state functional magnetic resonance imaging (rs-fMRI). Stepwise functional connectivity (SFC) was used to characterize the pattern of functional connectivity between sensory seed regions and the rest of the brain at direct, short, intermediate, and long functional connectivity distances, thus covering the continuum from the sensory input to the neural hubs supporting higher order cognitive functions. As compared to controls, adults with ADHD presented increased SFC degree within primary sensory regions and decreased SFC degree between sensory seeds and higher order integration nodes. In addition, they exhibited decreased connectivity degree between sensory seeds and regions of the default-mode network. Consistently, the higher the score in clinical severity scales the lower connectivity degree between seed regions and the default mode network.Entities:
Keywords: ADHD; adult ADHD; default mode network; resting-state fMRI; stepwise functional connectivity
Mesh:
Year: 2019 PMID: 31322305 PMCID: PMC6865796 DOI: 10.1002/hbm.24727
Source DB: PubMed Journal: Hum Brain Mapp ISSN: 1065-9471 Impact factor: 5.038