Growing out of attention deficit hyperactivity disorder: Insights from the ‘remitted’ brain

•We review neuroimaging studies of adults who have remitted from childhood ADHD.•Most studies find adult remitters show neural features indistinguishable from controls.•Fewer studies find that remission arises due to compensatory neural re-organization.•Some deep brain anomalies may persist from chi...

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Veröffentlicht in:Neuroscience and biobehavioral reviews 2018-11, Vol.94, p.198-209
Hauptverfasser: Sudre, Gustavo, Mangalmurti, Aman, Shaw, Philip
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Sprache:eng
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Zusammenfassung:•We review neuroimaging studies of adults who have remitted from childhood ADHD.•Most studies find adult remitters show neural features indistinguishable from controls.•Fewer studies find that remission arises due to compensatory neural re-organization.•Some deep brain anomalies may persist from childhood even in those who remit. We consider developmental and cognitive models to explain why some children ‘grow out’ of attention deficit hyperactivity disorder (ADHD) by adulthood. The first model views remission as a convergence towards more typical brain function and structure. In support, some studies find that adult remitters are indistinguishable from those who were never affected in the neural substrates of 'top-down' mechanisms of cognitive control, some 'bottom-up' processes of vigilance/response preparation, prefrontal cortical morphology and intrinsic functional connectivity. A second model postulates that remission is driven by the recruitment of new brain systems that compensate for ADHD symptoms. It draws support from demonstrations of atypical, but possibly beneficial, patterns of connectivity within the cognitive control network in adult remitters. The final model holds that some childhood ADHD anomalies show lifelong persistence, regardless of adult outcome, supported by shared reports of anomalies in remitters and persisters in posterior cerebral and striato-thalamic regions. The models are compatible: different processes driving remission might occur in different brain regions. These models provide a framework for future studies which might inform novel treatments to 'accelerate' remission.
ISSN:0149-7634
1873-7528
1873-7528
DOI:10.1016/j.neubiorev.2018.08.010