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A neuropathological study of vascular factors in late-life depression
A J Thomas1, I N Ferrier, R N Kalaria
1Department of Psychiatry, University of Newcastle upon Tyne, UK. a.j.thomas@ncl.ac.uk
Insights
Late-life depression is linked to increased atheromatous disease in major blood vessels, supporting the vascular depression hypothesis. However, no link was found with microvascular disease in the brain.
Area of Science:
- Neuropathology
- Geriatric Psychiatry
- Cardiovascular Disease
Background:
- Late-life depression is common and may involve vascular factors.
- Previous studies suggest a link, but direct neuropathological evidence was lacking.
- The
- vascular depression
- hypothesis requires investigation in postmortem brain tissue.
Purpose of the Study:
- To investigate neuropathological differences in late-life depression.
- To examine associations between depression and atheromatous disease in large/medium vessels.
- To assess microvascular disease in the brain in depressed elderly individuals.
Main Methods:
- Postmortem brain tissue from 20 depressed patients and 20 controls was analyzed.
- Alzheimer's and Lewy body pathologies were quantified.
- Atheromatous disease in aorta, coronary, and cerebral vessels was rated; brain microvascular disease was also assessed.
Main Results:
- No significant differences in age, sex, or postmortem delay between groups.
- Atheromatous disease was significantly increased in the depressed group (p=0.023).
- No differences in brain microvascular disease or significant Alzheimer's/Lewy body pathology were found.
Conclusions:
- Neuropathological evidence supports an excess of atheromatous disease in late-life depression.
- Findings indicate a link between vascular disease (aortic/cerebral vessels) and depression.
- The study broadly supports the vascular depression hypothesis, excluding microvascular disease as a factor.
Objectives:
Depression is a common psychiatric disorder in late life and it may be associated with vascular disease processes. Although there are clinical and neuroimaging studies lending support to such a "vascular depression" hypothesis there have been no neuropathological studies to directly test this. Postmortem tissue was investigated to determine whether late life depression was associated with atheromatous change in large and medium vessels and microvascular disease in the brain.
Methods:
Postmortem tissue was obtained from 20 patients with a history of at least one episode of DSM-IV major depression and 20 control subjects. Standard procedures were carried out to analyze and quantify Alzheimer type pathology (plaques, tangles, Braak staging) and cortical Lewy bodies. Coronary arteries, cerebral vessels, and aorta were rated for atheromatous disease on a 0-3 scale and the four neocortical areas were rated for microvascular disease.
Results:
The two groups showed no significant differences in age, sex, or postmortem delay. There was a significant increase in atheromatous disease in the depressed group (p=0.023). No differences were found for microvascular disease, either in the brain generally or locally in the frontal lobes. No subject had any significant Alzheimer type or Lewy body pathology.
Conclusions:
Neuropathological evidence was found for an excess of atheromatous disease, related to the aortic and cerebral vessels, in late life depression. However, there was no evidence of an increase in microvascular disease. The findings broadly support the vascular depression hypothesis.
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