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A volumetric study of MRI signal hyperintensities in late-life depression

Lookup NU author(s): Dr Michael FirbankORCiD, Dr Adrian Lloyd, Emeritus Professor Nicol Ferrier, Professor John O'Brien

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Abstract

Objective: An increase in white-matter lesions has been previously described in older subjects with depression. The authors investigated whether the regional location varied between depressed and normal subjects and determined the relationship of magnetic resonance (MR) signal hyperintensities to known clinical risk factors for vascular disease. Methods: Authors used automated image-processing software to determine volumes of signal hyperintensities from MR brain scans of older people with depression (N -29; mean age: 76 years) and normal subjects of similar age (N=32). Results: Overall, subjects with depression had a significantly greater frontal-lobe white-matter lesion volume than normal subjects (0.35% versus 0.22%). However, after excluding subjects with hypertension, diabetes, or ischemic heart disease (leaving 14 depressed and 15 normal subjects), we found even greater differences between groups, with a larger volume of MR signal hyperintensities in the frontal region of the depressed group, but no difference in the basal ganglia or parietal and occipital lobes. Conclusion: The results support the "vascular depression" hypothesis and suggest that those with depression but without traditional vascular risk factors may be much more susceptible to cerebrovascular disease than normal subjects. The mechanisms for this increased susceptibility remain to be determined. © 2004 American Association for Geriatric Psychiatry.


Publication metadata

Author(s): Firbank MJ, Lloyd AJ, Ferrier N, O'Brien JT

Publication type: Article

Publication status: Published

Journal: American Journal of Geriatric Psychiatry

Year: 2004

Volume: 12

Issue: 6

Pages: 606-612

Print publication date: 01/11/2004

ISSN (print): 1064-7481

ISSN (electronic): 1545-7214

Publisher: Lippincott Williams & Wilkins

URL: http://dx.doi.org/10.1176/appi.ajgp.12.6.606

DOI: 10.1176/appi.ajgp.12.6.606

PubMed id: 15545328


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