Caudate asymmetry is related to attentional impulsivity and an objective measure of ADHD-like attentional problems in healthy adults.

Published

Journal Article

Case-control studies comparing ADHD with typically developing individuals suggest that anatomical asymmetry of the caudate nucleus is a marker of attention deficit hyperactivity disorder (ADHD). However, there is no consensus on whether the asymmetry favors the right or left caudate nucleus in ADHD, or whether the asymmetry is increased or decreased in ADHD. The current study aimed to clarify this relationship by applying a dimensional approach to assessing ADHD symptoms that, instead of relying on clinical classification, utilizes the natural behavioral continuum of traits related to ADHD. Structural T1-weighted MRI was collected from 71 adults between 18 and 35 years and analyzed for caudate asymmetry. ADHD-like attentional symptoms were assessed with an objective measure of attentional problems, the ADHD score from the Test of Variables of Attention (TOVA). Impulsivity, a core feature in ADHD, was measured using the Barratt Impulsiveness Scale, a self-report measure that assesses attentional, non-planning, and motor features of impulsivity. We found that larger right relative to left caudate volumes correlated with both higher attentional impulsiveness and worse ADHD scores on the TOVA. Higher attentional impulsiveness also correlated with worse ADHD scores, establishing coherence between the objective measure and the self-report measure of attentional problems. These results suggest that a differential passage of information through frontal-striatal networks may produce instability leading to attentional problems. The findings also demonstrate the utility of a dimensional approach to understanding structural correlates of ADHD symptoms.

Full Text

Duke Authors

Cited Authors

  • Dang, LC; Samanez-Larkin, GR; Young, JS; Cowan, RL; Kessler, RM; Zald, DH

Published Date

  • January 2016

Published In

Volume / Issue

  • 221 / 1

Start / End Page

  • 277 - 286

PubMed ID

  • 25269835

Pubmed Central ID

  • 25269835

Electronic International Standard Serial Number (EISSN)

  • 1863-2661

International Standard Serial Number (ISSN)

  • 1863-2653

Digital Object Identifier (DOI)

  • 10.1007/s00429-014-0906-6

Language

  • eng