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Published on: March 23, 2011
Reductions in neuronal density in elderly depressed are region specific
Eric Van Otterloo1, Gillian O'Dwyer, Craig A Stockmeier
1Department of Psychiatry & Human Behavior, University of Mississippi Medical Center, Jackson, MS 39216-4505, USA.
Neuronal density in the dorsolateral prefrontal cortex (dlPFC) of elderly depressed individuals did not differ from controls. This suggests that neuropathology in geriatric depression is region-specific, unlike findings in the orbitofrontal cortex (ORB).
Area of Science:
- Neuroscience
- Geriatric Psychiatry
- Neuropathology
Background:
- Frontal regions, including the orbitofrontal cortex (ORB) and dorsolateral prefrontal cortex (dlPFC), are implicated in geriatric depression neuropathology.
- Previous studies reported reduced pyramidal neuron density in the ORB of older depressed subjects.
- The cellular pathology of the dlPFC in geriatric depression remained unexamined.
Purpose of the Study:
- To investigate the cellular pathology of the dorsolateral prefrontal cortex (dlPFC) in elderly individuals with major depression.
- To compare neuronal density and cortical width in the dlPFC between depressed elderly subjects and age-matched controls.
Main Methods:
- Postmortem dlPFC (Brodmann's area 9) tissue was obtained from 10 older depressed subjects and 10 controls.
- Pyramidal and non-pyramidal neuron density (overall and laminar) was measured using the linear optical disector method.
- Cortical and laminar widths were also assessed.
Main Results:
- No significant differences were found in the overall or laminar density of pyramidal or non-pyramidal neurons between depressed and control groups.
- Cortical and laminar widths in the dlPFC were not significantly affected by depression in the elderly.
- These findings contrast with previous observations of reduced pyramidal neuron density in the ORB.
Conclusions:
- Neuronal pathology in geriatric depression appears to be region-specific.
- The dlPFC does not show significant changes in neuronal density in elderly depressed individuals.
- These results highlight the need for further research into regional variations in brain pathology in geriatric depression.
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