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Updated: May 28, 2026

Exploring the Neural Correlates of Cognitive Reappraisal in Obsessive-Compulsive Disorder Using Task-based Functional Magnetic Resonance Imaging
Published on: March 14, 2025
MRSI correlates of cognitive-behavioral therapy in pediatric obsessive-compulsive disorder
Joseph O'Neill1, John C Piacentini, Susanna Chang
1Division of Child & Adolescent Psychiatry, Semel Institute for Neurosciences, Department of Radiological Sciences, UCLA School of Medicine, Los Angeles, CA 90024-1759, United States. joneill@mednet.ucla.edu
Insights
Cognitive-behavioral therapy (CBT) for pediatric obsessive-compulsive disorder (OCD) shows metabolic brain changes. Proton magnetic resonance spectroscopic imaging (1H MRSI) revealed altered metabolites in the pregenual anterior cingulate cortex (pACC) and thalamus, predicting treatment response.
Area of Science:
- Neuroscience
- Pediatric Psychiatry
- Radiology
Background:
- Cognitive-behavioral therapy (CBT) is effective for pediatric obsessive-compulsive disorder (OCD), but its brain mechanisms are unclear.
- Adult OCD neuroimaging suggests CBT impacts metabolism in the striatum, thalamus, and anterior cingulate cortex.
- Proton magnetic resonance spectroscopic imaging (1H MRSI) was used to investigate these metabolic effects in pediatric OCD.
Purpose of the Study:
- To explore the metabolic brain changes associated with CBT in pediatric OCD patients.
- To identify potential neuroimaging biomarkers for OCD and treatment response.
Main Methods:
- Proton magnetic resonance spectroscopic imaging (1H MRSI) was performed on 5 unmedicated pediatric OCD patients and 9 healthy controls.
- MRSI targeted the bilateral putamen, thalamus, and pregenual anterior cingulate cortex (pACC).
- Patients were rescanned after 12 weeks of exposure-based CBT, with symptom severity assessed using the Children's Yale-Brown Obsessive-Compulsive Scale (CY-BOCS).
Main Results:
- Four out of five patients showed a positive response to CBT, with a significant reduction in CY-BOCS scores.
- Pre-treatment, patients had higher N-acetyl-aspartate+N-acetyl-aspartyl-glutamate (tNAA) in the left pACC compared to controls.
- Post-treatment, decreased tNAA and creatine (Cr) in the left pACC and increased choline compounds (Cho) in the right thalamus were observed. Lower baseline tNAA, glutamate+glutamine (Glx), and myo-inositol (mI) in the left thalamus predicted a greater symptom reduction.
Conclusions:
- Metabolic alterations in the pACC and thalamus, measurable by MRSI, may serve as indicators of pediatric OCD.
- These metabolic changes correlate with treatment response to CBT, offering potential biomarkers for predicting treatment outcomes.
- Findings support the Glutamatergic Hypothesis of Pediatric OCD and highlight MRSI's utility in understanding treatment mechanisms.
Background:
The brain mechanisms of cognitive-behavioral therapy (CBT), a highly effective treatment for pediatric obsessive-compulsive disorder (OCD), are unknown. Neuroimaging in adult OCD indicates that CBT is associated with metabolic changes in striatum, thalamus, and anterior cingulate cortex. We therefore probed putative metabolic effects of CBT on these brain structures in pediatric OCD using proton magnetic resonance spectroscopic imaging (1H MRSI).
Method:
Five unmedicated OCD patients (4 ♀, 13.5±2.8) and 9 healthy controls (7 ♀, 13.0±2.5) underwent MRSI (1.5 T, repetition-time/echo-time=1500/30 ms) of bilateral putamen, thalamus and pregenual anterior cingulate cortex (pACC). Patients were rescanned after 12 weeks of exposure-based CBT. The Children's Yale-Brown Obsessive-Compulsive Scale (CY-BOCS) of OCD symptoms was administered before and after CBT.
Results:
Four of 5 patients responded to CBT (mean 32.8% CY-BOCS reduction). Multiple metabolite effects emerged. Pre-CBT, N-acetyl-aspartate+N-acetyl-aspartyl-glutamate (tNAA) in left pregenual anterior cingulate cortex (pACC) was 55.5% higher in patients than controls. Post-CBT, tNAA (15.0%) and Cr (23.9%) in left pACC decreased and choline compounds (Cho) in right thalamus increased (10.6%) in all 5 patients. In left thalamus, lower pre-CBT tNAA, glutamate+glutamine (Glx), and myo-inositol (mI) predicted greater post-CBT drop in CY-BOCS (r=0.98) and CY-BOCS decrease correlated with increased Cho.
Conclusions:
Interpretations are offered in terms of the Glutamatergic Hypothesis of Pediatric OCD. Similar to 18FDG-PET in adults, objectively measurable regional MRSI metabolites may indicate pediatric OCD and predict its response to CBT.
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