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Am J Psychiatry 2008; 165:116-123
(published online November 6, 2007; doi: 10.1176/appi.ajp.2007.07010143)
© 2008 American Psychiatric Association
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* Neurophysiology
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* Obsessive-Compulsive Disorder
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Increased Error-Related Brain Activity in Pediatric Obsessive-Compulsive Disorder Before and After Treatment

Greg Hajcak, Ph.D., Martin E. Franklin, Ph.D., Edna B. Foa, Ph.D., and Robert F. Simons, Ph.D.

OBJECTIVE: The error-related negativity is a negative deflection in the event-related potential maximal approximately 50 msec after the commission of errors. The error-related negativity is generated in the anterior cingulate cortex, and both anterior cingulate cortex hyperactivity and increased error-related brain activity have been reported in adults with obsessive-compulsive disorder (OCD). However, no study to date, to the authors’ knowledge, has examined error-related brain activity in pediatric patients with OCD, and no study has examined error-related brain activity in OCD both before and after treatment. METHOD: The error-related negativity was measured in 18 treatment-seeking pediatric patients with OCD and 18 age-matched comparison subjects. Of these patients, 10 returned for a second testing session after cognitive behavior therapy; 13 comparison children participated a second time after a comparable interval. RESULTS: In the pretreatment group, the error-related negativity was reliably larger in pediatric patients with OCD in relation to comparison subjects. This difference was also evident after treatment. There was no relationship between error-related negativity and symptom severity or changes in symptom severity. CONCLUSIONS: Consistent with studies in adult patients, increased error-related brain activity is evident in pediatric patients with OCD. Furthermore, increased error-related brain activity does not appear to change as a function of symptom reduction after therapy. These results suggest that an increased error-related negativity may be a trait-like marker for psychopathology and might be a useful endophenotype.




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