4.7 Article

Shared alterations in resting-state brain connectivity in adults with attention-deficit/hyperactivity disorder and their unaffected first-degree relatives

Journal

PSYCHOLOGICAL MEDICINE
Volume 51, Issue 2, Pages 329-339

Publisher

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291719003374

Keywords

Attention-deficit; hyperactivity disorder; default mode network; dimensional; endophenotype; functional connectivity; resting state; sustained attention

Funding

  1. Medical Research Council
  2. Wellcome Trust [G1000183, 093875/Z/10/Z]
  3. Medical Research Council Doctoral Training Grant
  4. Shanghai Municipal Science and Technology Major Project [2018SHZDZX01]
  5. National Institute of Health Research Biomedical Research Centre (Mental Health Theme)

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This study identified a neurocognitive trait in the default mode connectivity that is shared between adult ADHD probands and their first-degree relatives, associated with higher ADHD symptoms. This brain-based trait may serve as an important indicator in genetic studies and pharmaceutical development for ADHD.
Background Attention-deficit/hyperactivity disorder (ADHD) is a developmental condition that often persists into adulthood with extensive negative consequences on quality of life. Despite emerging evidence indicating the genetic basis of ADHD, investigations into the familial expression of latent neurocognitive traits remain limited. Methods In a group of adult ADHD probands (n = 20), their unaffected first-degree relatives (n = 20) and typically developing control participants (n = 20), we assessed endophenotypic alterations in the default mode network (DMN) connectivity during resting-state functional magnetic resonance imaging in relation to cognitive performance and clinical symptoms. In an external validation step, we also examined the dimensional nature of this neurocognitive trait in a sample of unrelated healthy young adults (n = 100) from the Human Connectome Project (HCP). Results The results illustrated reduced anti-correlations between the posterior cingulate cortex/precuneus and right middle frontal gyrus that was shared between adult ADHD probands and their first-degree relatives, but not with healthy controls. The observed connectivity alterations were linked to higher ADHD symptoms that was mediated by performance in a sustained attention task. Moreover, this brain-based neurocognitive trait dimensionally explained ADHD symptom variability in the HCP sample. Conclusions Alterations in the default mode connectivity may represent a dimensional endophenotype of ADHD, hence a significant aspect of the neuropathophysiology of this disorder. As such, brain network organisation can potentially be employed as an important neurocognitive trait to enhance statistical power of genetic studies in ADHD and as a surrogate efficacy endpoint in the development of novel pharmaceuticals.

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