4.1 Article

Orbitofrontal Cortex Volumes in Medication Naive Children with Major Depressive Disorder: A Magnetic Resonance Imaging Study

Journal

Publisher

MARY ANN LIEBERT, INC
DOI: 10.1089/cap.2007.053

Keywords

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Funding

  1. Krus Endowed Chair (UTH-SCSA)
  2. Joe F. Young Sr. Psychiatric Research and Training Program
  3. Miriam L. Hamburger Endowed Chair (Wayne State University)
  4. Mental Illness Research Association
  5. State of Michigan
  6. Japan Foundation for Aging and Health
  7. CAPES Foundation (Brazil)
  8. [MH01736]
  9. [MH068662]
  10. [MH59299]
  11. [MH65122]
  12. [MH02037]
  13. [RR 020571]

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Objectives: Adults with major depressive disorder (MDD) are reported to have reduced orbitofrontal cortex (OFC) volumes, which could be related to decreased neuronal density. We conducted a study on medication naive children with MDD to determine whether abnormalities of OFC are present early in the illness course. Methods: Twenty seven medication naive pediatric Diagnostic and Statistical Manual of Mental Disorders, 4(th) edition (DSM-IV) MDD patients (mean age +/- SD = 14.4 +/- 2.2 years; 10 males) and 26 healthy controls (mean age +/- SD = 14.4 +/- 2.4 years; 12 males) underwent a 1.5T magnetic resonance imaging (MRI) with 3D spoiled gradient recalled acquisition. The OFC volumes were compared using analysis of covariance with age, gender, and total brain volume as covariates. Results: There was no significant difference in either total OFC volume or total gray matter OFC volume between MDD patients and healthy controls. Exploratory analysis revealed that patients had unexpectedly larger total right lateral (F = 4.2, df = 1, 48, p = 0.05) and right lateral gray matter (F = 4.6, df = 1, 48, p = 0.04) OFC volumes compared to healthy controls, but this finding was not significant following statistical correction for multiple comparisons. No other OFC subregions showed a significant difference. Conclusions: The lack of OFC volume abnormalities in pediatric MDD patients suggests the abnormalities previously reported for adults may develop later in life as a result of neural cell loss.

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