The ability to maintain cognition despite the accumulation of AD pathology is known as cognitive or neural reserve. Theories of neural reserve include brain reserve capacity, and neural efficiency or compensation, i.e., brains differ in their response to the accumulation of AD pathology. In the initial funding period we found that many older persons without dementia or MCI meet pathologic criteria for AD, indicating that other factors must be involved in determining the extent to which AD pathology impairs cognition. We found that AD pathology often does not cause dementia in the absence of cerebral infarcts and Lewy bodies. Further, we found that loneliness, psychological distress, and cognitive activity were all related to incident AD, but were not related to measures of AD pathology, infarcts, or Lewy bodies, suggesting that other as yet unknown factors can alter brain reserve capacity. Finally, we found that the relation of AD pathology to cognition varied by social network size and level of processing resources (working memory and perceptual speed), consistent with neural efficiency or compensation. The proposed continuation of the Rush Memory and Aging Project, a community-based longitudinal epidemiologic study of risk factors for incident AD that includes brain donation at death, will build on findings from the initial funding period. The choice of risk factors was guided by the recommendations of the recent Cognitive and Emotional Health Project. The renewal is organized into three conceptual themes linking factors to incident AD and neuropathology. Specifically, we hypothesize that a) apolipoprotein E allele status, diabetes, and pulmonary function will be associated with incident AD via cerebrovascular pathology;b) the relation of neuropathology to cognition will vary by level of life course SES and physical activity;and c) depressive symptoms and parkinsonian signs will predict incident AD, but will actually represent early non-cognitive manifestations of AD pathology in neuronal populations subserving affective behavior and motor function, respectively. Since prevention is the best long-term strategy for reducing the burden of cognitive impairment in the U.S., and understanding the neurobiologic pathways linking risk factors to cognition is essential for the development of therapeutic interventions, the proposed study, with its involvement of community dwelling older men and women as subjects with a wide range of SES, is in a position to provide new knowledge critical to public health. The prevention of Alzheimer's disease provides the best long-term strategy to reduce the human and economic toll of disease, and understanding the biologic pathways linking risk factors to cognition is essential for developing therapeutic interventions. Thus, the proposed epidemiologic study of risk factors for AD that includes organ donation, with its involvement of community dwelling older men and women with a wide range of socioeconomic status, is in a position to provide new knowledge critical to public health.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG017917-10
Application #
8293179
Study Section
Neurological, Aging and Musculoskeletal Epidemiology (NAME)
Program Officer
Anderson, Dallas
Project Start
2000-03-01
Project End
2014-06-30
Budget Start
2012-07-01
Budget End
2014-06-30
Support Year
10
Fiscal Year
2012
Total Cost
$1,684,096
Indirect Cost
$531,328
Name
Rush University Medical Center
Department
Type
Schools of Medicine
DUNS #
068610245
City
Chicago
State
IL
Country
United States
Zip Code
60612
Ridge, Perry G; Hoyt, Kaitlyn B; Boehme, Kevin et al. (2016) Assessment of the genetic variance of late-onset Alzheimer's disease. Neurobiol Aging 41:200.e13-20
Buchman, Aron S; Yu, Lei; Boyle, Patricia A et al. (2016) Higher brain BDNF gene expression is associated with slower cognitive decline in older adults. Neurology 86:735-41
Han, S Duke; Boyle, Patricia A; Arfanakis, Konstantinos et al. (2016) Financial literacy is associated with white matter integrity in old age. Neuroimage 130:223-9
Han, S Duke; Boyle, Patricia A; James, Bryan D et al. (2016) Mild Cognitive Impairment and Susceptibility to Scams in Old Age. J Alzheimers Dis 49:845-51
Morris, Martha Clare; Brockman, John; Schneider, Julie A et al. (2016) Association of Seafood Consumption, Brain Mercury Level, and APOE ε4 Status With Brain Neuropathology in Older Adults. JAMA 315:489-97
Wilson, Robert S; Boyle, Patricia A; Capuano, Ana W et al. (2016) Late-life depression is not associated with dementia-related pathology. Neuropsychology 30:135-42
Han, S Duke; Boyle, Patricia A; James, Bryan D et al. (2016) Discrepancies between cognition and decision making in older adults. Aging Clin Exp Res 28:99-108
Perlman, Amichai; Shah, Raj C; Bennett, David A et al. (2016) Antihypertensive and Statin Medication Use and Motor Function in Community-Dwelling Older Adults. J Am Med Dir Assoc 17:220-4
Chouraki, Vincent; Reitz, Christiane; Maury, Fleur et al. (2016) Evaluation of a Genetic Risk Score to Improve Risk Prediction for Alzheimer's Disease. J Alzheimers Dis 53:921-32
Roostaei, T; Nazeri, A; Felsky, D et al. (2016) Genome-wide interaction study of brain beta-amyloid burden and cognitive impairment in Alzheimer's disease. Mol Psychiatry :

Showing the most recent 10 out of 384 publications