Original Article
Endogenous sex hormones, cognitive decline, and future dementia in old men
Article first published online: 24 JUL 2006
DOI: 10.1002/ana.20918
Copyright © 2006 American Neurological Association
Additional Information
How to Cite
Geerlings, M. I., Strozyk, D., Masaki, K., Remaley, A. T., Petrovitch, H., Ross, G. W., White, L. R. and Launer, L. J. (2006), Endogenous sex hormones, cognitive decline, and future dementia in old men. Ann Neurol., 60: 346–355. doi: 10.1002/ana.20918
Publication History
- Issue published online: 18 SEP 2006
- Article first published online: 24 JUL 2006
- Manuscript Accepted: 20 MAY 2006
- Manuscript Revised: 19 MAY 2006
- Manuscript Received: 30 JAN 2006
Funded by
- National Institute on Aging [NIA]
- “Epidemiology of Brain Aging in the Very Old”. Grant Number: 5UO1AG09349
- “Epidemiology of Aging and Dementia–Autopsy Research”. Grant Number: 2 RO1AG07155
- Intramural Research Program of the NIA
- National Heart, Lung, and Blood Institute. Grant Number: NO1-HC-05102
- American Heart Association. Grant Number: 95-014560
- Abstract
- Article
- References
- Cited By
Abstract
Objective:
To estimate the association of endogenous levels of bioavailable testosterone and estradiol with risk for cognitive decline and dementia in old men.
Methods:
Within the population-based, prospective Honolulu-Asia Aging Study, 2,974 men, aged 71 to 93 years, without dementia were reexamined 3 times over an average of 6 years for development of dementia and cognitive decline. Cognitive decline was measured with the Cognitive Abilities Screening Instrument. Incident dementia was diagnosed according to standard criteria. A total of 134 men experienced development of Alzheimer's disease (AD; including 40 cases with contributing cerebrovascular disease) and 44 experienced development of vascular dementia.
Results:
Adjusting for age and other covariates, testosterone was not associated with risk for dementia (using Cox regression analyses) or cognitive decline (using random coefficient analyses). However, higher levels of estradiol were associated with risk for AD (hazard ratio per standard deviation increase, 1.25; 95% confidence interval, 1.05–1.47) and AD with cerebrovascular disease (hazard ratio, 1.19; 95% confidence interval, 1.02–1.38). Also, compared with the lowest tertile of estradiol, men in the middle and highest tertile of estradiol had 0.24 and 0.28 points lower Cognitive Abilities Screening Instrument scores, respectively, for each year increase in age.
Interpretation:
In old men, endogenous testosterone levels are not associated with risk for cognitive decline and AD, whereas higher estrogen levels increase risk for cognitive decline and AD. Ann Neurol 2006.

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