• Brian P Brennan, Olga Tkachenko, Zachary J Schwab, Richard J Juelich, Erin M Ryan, Alison J Athey, Harrison G Pope, Michael A Jenike, Justin T Baker, William D S Killgore, James I Hudson, J Eric Jensen, and Scott L Rauch.
• 1] Biological Psychiatry Laboratory, McLean Hospital, Belmont, MA, USA [2] Obsessive-Compulsive Disorders Institute, McLean Hospital, Belmont, MA, USA [3] Department of Psychiatry, Harvard Medical School, Boston, MA, USA.
• Neuropsychopharmacology. 2015 Jul 1; 40 (8): 1866-76.

AbstractThe anterior cingulate cortex is implicated in the neurobiology of obsessive-compulsive disorder (OCD). However, few studies have examined functional and neurochemical abnormalities specifically in the rostral subdivision of the ACC (rACC) in OCD patients. We used functional magnetic resonance imaging (fMRI) during an emotional counting Stroop task and single-voxel J-resolved proton magnetic resonance spectroscopy ((1)H-MRS) in the rACC to examine the function and neurochemistry of the rACC in individuals with OCD and comparison individuals without OCD. Between-group differences in rACC activation and glutamine/glutamate ratio (Gln/Glu), Glu, and Gln levels, as well as associations between rACC activation, Gln/Glu, Glu, Gln, behavioral, and clinical measures were examined using linear regression. In a sample of 30 participants with OCD and 29 age- and sex-matched participants without OCD, participants with OCD displayed significantly reduced rACC deactivation compared with those without OCD in response to OCD-specific words versus neutral words on the emotional counting Stroop task. However, Gln/Glu, Glu, and Gln in the rACC did not differ between groups nor was there an association between reduced rACC deactivation and Gln/Glu, Glu, or Gln in the OCD group. Taken together, these findings strengthen the evidence for rACC dysfunction in OCD, but weigh against an underlying association with abnormal rACC glutamatergic neurotransmission.

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