Changes in regional cerebral blood flow following antidepressant treatment in late‐life depression
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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In imaging studies of traditional antidepressant treatment response, increased cortical thickness and cerebral blood flow in the PFC correlate with efficacy.
“In imaging studies of traditional antidepressant treatment response, increased cortical thickness and cerebral blood flow in the PFC correlate with efficacy (108–112).”
From Psychedelics and Other Psychoplastogens for Treating Mental Illness. (2021) · cites this paper as [110]
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References 40 · Cited by 68
- Authors
- Ishizaki, J., Yamamoto, H., Takahashi, T., Takeda, M., Yano, M., & Mimura, M.
- Affiliations
- SHOWA Medical University (JP)
- Corresponding author
- Mimura, Masaru
- ORCID
- Mimura, Masaru
- Venue
- International Journal of Geriatric Psychiatry
- Publisher
- Wiley
- Published
- 2008-07-24
- Volume
- 23
- Issue
- 8
- Pages
- 805-811
- ISSN
- 0885-6230 (ISSN-L)
- 1099-1166
- OpenAlex
- W2094377152
- Cited by
- 68
- References
- 40
- Citations by year
- 2026: 3 · 2025: 4 · 2024: 1 · 2023: 1 · 2022: 2 · 2021: 3 · 2020: 3 · 2019: 5 · 2018: 2 · 2017: 6 · 2016: 6 · 2015: 2 · 2014: 6 · 2013: 3 · 2012: 2
- FWCI
- 4.45
- Type
- journal article
- Language
- en
- Open access
- closed
- Locations
- International Journal of Geriatric Psychiatry (publishedVersion)
- PubMed (publishedVersion)
- Topics
- Health Sciences › Medicine › Pharmacology › Treatment of Major Depression
- Life Sciences › Neuroscience › Cognitive Neuroscience › Neural and Behavioral Psychology Studies
- Life Sciences › Neuroscience › Cellular and Molecular Neuroscience › Neurotransmitter Receptor Influence on Behavior
- Keywords
- geriatric depression, regional cerebral blood flow, antidepressant treatment, pharmacotherapy, dorsolateral prefrontal cortex, anterior cingulate cortex, ventrolateral prefrontal cortex, parieto-occipital cortex, temporal lobe, remission, brain dysfunction, unipolar major depression
- MeSH terms
- Aged, Antidepressive Agents, Brain, Cerebral Cortex, Cerebrovascular Circulation, Depressive Disorder, Major, Major Depressive Disorder, Depressive Disorder, Female, Humans, Male, Middle Aged, Regional Blood Flow, Tomography, Emission-Computed, Single-Photon, Case-Control Studies, Prefrontal Cortex
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