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August 31, 2010; 75 (9) Articles

Change in risk of Alzheimer disease over time

L.E. Hebert, J.L. Bienias, N.T. Aggarwal, R.S. Wilson, D.A. Bennett, R.C. Shah, D.A. Evans
First published August 30, 2010, DOI: https://doi.org/10.1212/WNL.0b013e3181f0754f
L.E. Hebert
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J.L. Bienias
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N.T. Aggarwal
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R.S. Wilson
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D.A. Bennett
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R.C. Shah
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Citation
Change in risk of Alzheimer disease over time
L.E. Hebert, J.L. Bienias, N.T. Aggarwal, R.S. Wilson, D.A. Bennett, R.C. Shah, D.A. Evans
Neurology Aug 2010, 75 (9) 786-791; DOI: 10.1212/WNL.0b013e3181f0754f

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Abstract

Objective: To assess whether the risk of incidence of Alzheimer disease (AD) varies over time. The increase in numbers of people at the oldest ages in the population will bring an increase in the number of people with AD. Projections of the size of the increase assume the risk of AD is constant.

Methods: All persons age 65 or older in a biracial, geographically defined area were invited to participate in a home interview every 3 years. From the approximately 10,000 participants, stratified random samples were selected for detailed clinical evaluation. At each cycle, individuals determined free of AD in a previous cycle, either by examination or by high score on cognitive function tests, were sampled in the subsequent cycle for evaluation for incident AD. The evaluations for disease were structured and uniform across time. These analyses include 1,695 subjects evaluated for incident disease from 1997 through 2008.

Results: AD developed in 360 participants. Change over time in risk of incident disease was assessed in logistic regression analyses including evaluation date and controlling for age, gender, education, race, interval from disease-free designation to evaluation for incident disease, and sample design. The time variable (in years) was not significant (odds ratio = 0.970, 95% confidence interval = 0.902 to 1.044).

Conclusions: The null relation of evaluation date to disease incidence suggests no recent change in risk of AD over time, and supports this assumption for projections of AD.

Footnotes

  • See page 779

    Study funding: Supported by the NIH/NIA AG029652 and AG11101.

    Disclosure: Author disclosures are provided at the end of the article.

    Received March 16, 2010. Accepted in final form May 24, 2010.

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