4.7 Article

Comparison of neural substrates of temporal discounting between youth with autism spectrum disorder and with obsessive-compulsive disorder

期刊

PSYCHOLOGICAL MEDICINE
卷 47, 期 14, 页码 2513-2527

出版社

CAMBRIDGE UNIV PRESS
DOI: 10.1017/S0033291717001088

关键词

ASD; fMRI; OCD; temporal discounting

资金

  1. Medical Research Council [MRC G0300155]
  2. MRC UK Autism Imaging Multicentre Study [G0400061]
  3. National Institute for Health Research (NIHR) Biomedical Research Centre at South London and Maudsley NHS Foundation Trust and King's College London
  4. MRC [G0300155]
  5. Institute of Psychiatry, Psychology and Neuroscience, King's College London
  6. NIHR-BRC
  7. MRC [G0300155, MR/N026063/1] Funding Source: UKRI
  8. Medical Research Council [MR/N026063/1, G0300155] Funding Source: researchfish
  9. National Institute for Health Research [RP-PG-0606-1045] Funding Source: researchfish

向作者/读者索取更多资源

Background. Autism spectrum disorder (ASD) and obsessive-compulsive disorder (OCD) share abnormalities in hot executive functions such as reward-based decision-making, as measured in the temporal discounting task (TD). No studies, however, have directly compared these disorders to investigate common/distinct neural profiles underlying such abnormalities. We wanted to test whether reward-based decision-making is a shared transdiagnostic feature of both disorders with similar neurofunctional substrates or whether it is a shared phenotype with disorder-differential neurofunctional underpinnings. Methods. Age and IQ-matched boys with ASD (N= 20), with OCD (N= 20) and 20 healthy controls, performed an individually-adjusted functional magnetic resonance imaging (fMRI) TD task. Brain activation and performance were compared between groups. Results. Boys with ASD showed greater choice-impulsivity than OCD and control boys. Whole-brain between-group comparison revealed shared reductions in ASD and OCD relative to control boys for delayed-immediate choices in right ventromedial/lateral orbitofrontal cortex extending intomedial/inferior prefrontal cortex, and in cerebellum, posterior cingulate and precuneus. For immediate-delayed choices, patients relative to controls showed reduced activation in anterior cingulate/ventromedial prefrontal cortex reaching into left caudate, which, at a trend level, was more decreased in ASD than OCD patients, and in bilateral temporal and inferior parietal regions. Conclusions. This first fMRI comparison between youth with ASD and with OCD, using a reward-based decision-making task, shows predominantly shared neurofunctional abnormalities during TD in key ventromedial, orbital-and inferior fronto-striatal, temporo-parietal and cerebellar regions of temporal foresight and reward processing, suggesting trans-diagnostic neurofunctional deficits.

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