Toggle Main Menu Toggle Search

Open Access padlockePrints

A Longitudinal Study of Hippocampal Volume, Cortisol Levels, and Cognition in Older Depressed Subjects

Lookup NU author(s): Professor John O'Brien, Dr Adrian Lloyd, Professor Ian McKeith, Dr Anil Gholkar OBE, Emeritus Professor Nicol Ferrier

Downloads

Full text for this publication is not currently held within this repository. Alternative links are provided below where available.


Abstract

Objective:This study determined whether cognitive impairments and structural brain changes in older depressed subjects, especially in the hippocampus, are related to hypercortisolemia. Method: Sixty-one depressed subjects over age 60 who met DSM-IV criteria for major depression and 40 healthy comparison subjects underwent structural magnetic resonance imaging, neuropsychological testing, apolipoprotein E (APOE) genotyping, and salivary cortisol assessment (over 3 days) with follow-up 6 months later. Hippocampal volume was measured by manual segmentation that was blind to diagnosis. Average area under the curve for salivary cortisol over the 3 days was calculated. Cognitive function was assessed by using a combined memory z score. Results: Depressed subjects showed multiple impairments in attention, working memory, visual memory, verbal memory, new learning, and executive function in relation to comparison subjects. They had hypercortisolemia (53% increase in area under the curve) and a reduction in right hippocampal volume (6% decrease). Hippocampal volume reduction was not associated with increased cortisol levels but was significantly correlated with continuing memory deficits at 6 months. Persisting "mild cognitive impairment" was seen in 20 (41%) of 49 subjects at 6 months and was associated with reduced hippocampal volume but not severity of depression, cortisol levels, or APOE genotype. Conclusions: Older depressed subjects have persisting cognitive impairments associated with hippocampal volume reduction, but the results do not support cortisol-mediated hippocampal neurotoxicity as the major etiological mechanism. Neuropathological studies are required to investigate the basis for hippocampal changes, while follow-up will determine whether hippocampal atrophy is a risk factor for cognitive decline.


Publication metadata

Author(s): O'Brien JT, Lloyd A, McKeith I, Gholkar A, Ferrier N

Publication type: Article

Publication status: Published

Journal: American Journal of Psychiatry

Year: 2004

Volume: 161

Issue: 11

Pages: 2081-2090

ISSN (print): 0002-953X

ISSN (electronic): 1535-7228

Publisher: American Psychiatric Association

URL: http://dx.doi.org/10.1176/appi.ajp.161.11.2081

DOI: 10.1176/appi.ajp.161.11.2081


Altmetrics

Altmetrics provided by Altmetric


Share