Subjective memory complaints in aging are associated with elevated cortisol levels.

TitleSubjective memory complaints in aging are associated with elevated cortisol levels.
Publication TypeJournal Article
Year of Publication2005
AuthorsWolf OT, Dziobek I, McHugh P, Sweat V, de Leon MJ, Javier E, Convit A
JournalNeurobiol Aging
Volume26
Issue10
Pagination1357-63
Date Published2005 Nov-Dec
ISSN0197-4580
KeywordsAdrenocorticotropic Hormone, Aging, Analysis of Variance, Body Mass Index, Circadian Rhythm, Corticotropin-Releasing Hormone, Demography, Depression, Dexamethasone, Enzyme-Linked Immunosorbent Assay, Female, Humans, Hydrocortisone, Hypothalamo-Hypophyseal System, Male, Memory Disorders, Middle Aged, Neuropsychological Tests, Pituitary-Adrenal System, Psychological Tests, Radioimmunoassay, Sex Factors, Surveys and Questionnaires
Abstract

The origin and clinical significance of subjective memory complaints among middle aged and older individuals is not well understood. Associations with objective memory impairments, personality traits or mood disturbances have been reported. Elevated cortisol levels occur in aging and depression and causal links to cognitive or emotional problems have been suggested. The goal of this study was to investigate the associations between basal and feedback indices of cortisol regulation and subjective memory impairment in a sample of healthy middle aged and older subjects (mean age 61.8 years) with (n=27) and without (n=19) subjective memory complaints. Participants with memory complaints had both higher basal cortisol levels and higher cortisol levels after dexamethasone. There was a significant group by gender interaction for basal cortisol levels, where women without memory complaints showed significantly lower cortisol levels, whereas no such difference was found for the men. All effects were not due to slight differences in depression scores. Differences in personality traits or in stress susceptibility might underlie the present findings. Future studies of memory complaints should take a comprehensive approach including relevant endocrine parameters.

DOI10.1016/j.neurobiolaging.2004.11.003
Alternate JournalNeurobiol Aging
PubMed ID16243606
Grant ListR01 AG022374 / AG / NIA NIH HHS / United States
M01 RR00096 / RR / NCRR NIH HHS / United States
P30 AG08051 / AG / NIA NIH HHS / United States
R01-AG17115 / AG / NIA NIH HHS / United States
Related Institute: 
Brain Health Imaging Institute (BHII)

Weill Cornell Medicine
Department of Radiology
525 East 68th Street New York, NY 10065