Neurophysiology of perceptual decision-making and its alterations in attention-deficit hyperactivity disorder (ADHD)

  1. Mark A. Bellgrove1
  1. 1The Turner Institute for Brain and Mental Health, School of Psychological Sciences, Monash University, Victoria 3800, Australia
  2. 2School of Engineering, Cardiff University, Cardiff, Wales, United Kingdom
  3. 3Queensland Brain Institute, University of Queensland, Queensland 4067, Australia
  4. 4School of Psychology, Dublin City University, Dublin, Ireland
  5. 5Trinity College Institute of Neuroscience and School of Psychology, Trinity College Dublin, Dublin D02 PX31, Ireland
  1. Correspondence should be addressed to Mana Biabani at mana.biabani{at}monash.edu; Mark A. Bellgrove at Mark.Bellgrove{at}monash.edu
  1. Author contributions: M.B., J.W., A.J., and J.P. performed research; M.B., B.J., G.L., and M.B. contributed unpublished reagents/analytic tools; M.B., K.W., S.Z., and G.L. analyzed data; M.B. wrote the first draft of the paper; M.B., K.W., S.Z., J.W., A.J., J.P., N.M., B.J., G.L., R.O., and M.B. edited the paper; M.B. wrote the paper; N.M., R.O., and M.B. designed research.

Abstract

Despite the prevalence of ADHD, efforts to develop a detailed understanding of the neuropsychology of this neurodevelopmental condition are complicated by the diversity of interindividual presentations and the inability of current clinical tests to distinguish between its sensory, attentional, arousal or motoric contributions. Identifying objective methods that can explain the diverse performance profiles across individuals diagnosed with ADHD has been a long-held goal. Achieving this could significantly advance our understanding of etiological processes and potentially inform the development of personalized treatment approaches. Here, we examine key neuropsychological components of ADHD within an electrophysiological (EEG) perceptual decision-making paradigm that is capable of isolating distinct neural signals of several key information processing stages necessary for sensory-guided actions from attentional selection to motor responses. Using a perceptual decision-making task (random dot motion), we evaluated the performance of 79 children (aged 8 to 17 years) and found slower and less accurate responses, along with a reduced rate of evidence accumulation (drift rate parameter of drift diffusion model), in children with ADHD (n = 37; 13 female) compared to typically developing peers (n = 42; 18 female). This was driven by the atypical dynamics of discrete electrophysiological signatures of attentional selection, the accumulation of sensory evidence, and strategic adjustments reflecting urgency of response. These findings offer an integrated account of decision-making in ADHD and establish discrete neural signals that might be used to understand the wide range of neuropsychological performance variations in individuals with ADHD.

Significance Statement The efficacy of diagnostic and therapeutic pathways in ADHD is limited by our incomplete understanding of its neurological basis. One promising avenue of research is the search for basic neural mechanisms that may contribute to the variety of cognitive challenges associated with ADHD. We developed a mechanistic account of differences in a fundamental cognitive process by integrating across neurocognitive, neurophysiological (i.e., EEG), and computational levels of analysis. We detected distinct neural changes in ADHD that explained altered performance (e.g., slowed and less accurate responses). These included changes in neural patterns of attentional selection, sensory information processing, and response preparation. These findings enhance our understanding of the neurophysiological profile of ADHD and may offer potential targets for more effective, personalized interventions.

Footnotes

  • This work is supported by grants from the National Health and Medical Research Council (NHMRC) of Australia to M.A.B (#s2010899; 2025415)

  • The authors declare no competing financial interests.

  • Received March 11, 2024.
  • Revision received January 12, 2025.
  • Accepted January 22, 2025.