Dorsolateral prefrontal cortex and anterior cingulate cortex white matter alterations in late-life depression

Biol Psychiatry. 2006 Dec 15;60(12):1356-63. doi: 10.1016/j.biopsych.2006.03.052. Epub 2006 Jul 28.


Background: The dorsolateral prefrontal cortex (DLPFC) and anterior cingulate cortex (ACC) are critical for mood regulation. Alterations in the white matter connections of these regions may impair their role in mood regulation and increase the risk of developing depression. This study used diffusion tensor imaging to examine for white matter microstructural abnormalities of these regions and of central white matter structures in late-life depression.

Methods: One hundred six elderly depressed subjects and eighty-four elderly nondepressed subjects underwent clinical assessment and diffusion tensor imaging. The apparent diffusion coefficient (ADC) and fractional anisotropy (FA) were measured in regions of interest placed in the white matter of the DLPFC, ACC, corpus callosum, and internal capsule. Differences between groups were assessed, controlling for age, sex, and total cerebral volume.

Results: After controlling for covariates, depressed subjects had significantly lower FA values in white matter of the right ACC, bilateral superior frontal gyri, and left middle frontal gyrus. There were no significant differences in ADC values.

Conclusions: Lower FA, representing lower tissue organization, is observed in depressed elders in the DLPFC and right ACC. These findings support the hypothesis that altered connectivity between brain regions contributes to the risk of depression.

Publication types

  • Comparative Study
  • Research Support, N.I.H., Extramural

MeSH terms

  • Aged / psychology*
  • Aged, 80 and over
  • Anisotropy
  • Brain / anatomy & histology
  • Corpus Callosum / pathology
  • Cross-Sectional Studies
  • Data Interpretation, Statistical
  • Depressive Disorder / pathology*
  • Diffusion Magnetic Resonance Imaging
  • Female
  • Gyrus Cinguli / pathology*
  • Humans
  • Image Processing, Computer-Assisted
  • Male
  • Middle Aged
  • Prefrontal Cortex / pathology*
  • Psychiatric Status Rating Scales
  • Reproducibility of Results