Psychiatry Research
Volume 120, Issue 3 , Pages 265-271, 15 October 2003

Reduced response-inhibition in obsessive–compulsive disorder measured with topographic evoked potential mapping

Psychiatric Neurophysiology, Department of Psychiatry and Psychotherapy, University Hospital of Psychiatry and Psychotherapy, Füchsleinstraße 15, Würzburg 97080, Germany

Received 16 July 2002; received in revised form 24 June 2003; accepted 8 July 2003.

Abstract 

Recent neuroimaging studies have suggested that a hyperactivity of the frontal-striate neuronal circuits, including the orbitofrontal cortex and the basal ganglia, mediates the symptomatology of obsessive–compulsive disorder (OCD). However, there is also some evidence that the superior frontal cortex is less activated in OCD, and this local hypoactivity has been shown to be negatively associated with the symptomatology. As the superior frontal cortex is believed to be involved in inhibitory control, this study investigated the brain electrical activity during response inhibition in OCD. Twelve patients with OCD and 12 healthy controls performed a cued Go–NoGo task (continuous performance test), while event-related potentials were registered with 21 electrodes. Patients reacted significantly faster than controls, but did not differ from controls regarding the error rate. As a main result, we found a reduced frontal activity during the NoGo condition in OCD, which was condensed in a reduced anteriorisation of the brain electrical field. We suggest that this inhibitory deficit in OCD has a major contribution to the pathophysiology of OCD, which is underscored by the fact that the anteriorisation during the NoGo condition (NGA) was negatively correlated with the symptomatology as measured by the Yale-Brown Obsessive-Compulsive Scale.

Keywords: Inhibition, ERP, OCD, NoGo, CPT, P300

To access this article, please choose from the options below

Login to an existing account or Register a new account.

  • Purchase this article for 31.50 USD (You must login/register to purchase this article)

    Online access for 24 hours. The PDF version can be downloaded as your permanent record.

  • Subscribe to this title

    Get unlimited online access to this article and all other articles in this title 24/7 for one year.

  • Claim access now

    For current subscribers with Society Membership or Account Number.

  • Visit SciVerse ScienceDirect to see if you have access via your institution.
 

PII: S0165-1781(03)00188-4

doi:10.1016/S0165-1781(03)00188-4

Psychiatry Research
Volume 120, Issue 3 , Pages 265-271, 15 October 2003