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Changes in regional cerebral blood flow following antidepressant treatment in late-life depression

✍ Scribed by Junko Ishizaki; Hideki Yamamoto; Taro Takahashi; Maki Takeda; Madoka Yano; Masaru Mimura


Publisher
John Wiley and Sons
Year
2008
Tongue
English
Weight
153 KB
Volume
23
Category
Article
ISSN
0885-6230

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✦ Synopsis


Abstract

Objective

Reversible/irreversible abnormalities of regional cerebral blood flow (rCBF) are seen in patients with depression. However, in late‐life depression there is little evidence of a longitudinal change in rCBF through remission. We examined whether the decreased rCBF in individuals with late‐life depression resolves following treatment.

Methods

Twenty‐five depressed patients older than 55 years completed the Hamilton Rating Scale for Depression and single photon emission computed tomography before and after a mean of 13.7 weeks of pharmacotherapy. Quantitative analyses were performed using the Statistical Parametric Mapping procedure.

Results

Patients with depression demonstrated decreased rCBF in the anterior ventral and dorsal medial prefrontal cortex (PFC), including anterior cingulate cortices, bilateral ventrolateral PFC to temporal cortices, and bilateral medial to lateral parieto‐occipital lobes relative to healthy controls. No particular areas showed increased rCBF. Following pharmacotherapy, rCBF significantly increased in the left dorsolateral PFC to precentral areas and the right parieto‐occipital regions. However, decreased rCBF at baseline in the anterior ventral/dorsal medial PFC, bilateral ventrolateral PFC, bilateral temporal lobes, and bilateral parietal lobes did not show significant improvement after treatment.

Conclusions

Remarkable improvements in rCBF in the left dorsolateral PFC to precentral regions are consistent with the hypothesis that neuronetworks including the left frontal cortex may be functionally and reversibly involved in late‐life unipolar major depression (state‐dependent). In contrast, neural circuits including bilateral medial, dorsolateral, and parietal areas may reflect underlying and continuous pathognomonic brain dysfunction of depression (trait‐dependent). Copyright © 2008 John Wiley & Sons, Ltd.


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