Memory and Aging Project
The overall goal of the Memory and Aging Project is to identify the structural bases of neural reserve and examine the neurobiologic mechanisms through which environmental and genetic risk factors lead to the functional consequences of four neurologic diseases of aging.
- Start Year
- 1997
- Supplementary Information
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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.
Data/Bio-specimen Access: To apply for access to RADC data/tissue, please enter an electronic request at our website: https://www.radc.rush.edu/res/ext/home.htm.
| Investigators | Contacts |
|---|---|
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Design
- Study design
- Cohort
- Follow Up
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Annual follow-up
Marker Paper
Bennett DA, Schneider JA, Buchman AS, Barnes LL, Boyle PA, Wilson RS. Overview and Findings From the Rush Memory and Aging Project. Curr Alzheimer Res. 2012; 9(6):646-663.
PUBMED 22471867
Recruitment
- Recruitment Target
-
- Individuals
Number of Participants
- Number of Participants
- 1,700
- Number of Participants with Biological Samples
- 1,700
Access
Availability of data and biosamples
| Possible Access to Data | |
| Possible Access to Biosamples | |
| Other |
Timeline
MAP - Population
All participants agree to annual follow-up and donation of brain, spinal cord, muscle and nerve up on death.
Selection Criteria
- Minimum age
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65
- Newborns
- Twins
- Countries
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- United States of America
- Territory
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Chicagoland area
- Ethnic Origin
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- Health Status
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- Not demented at baseline
Recruitment
- Sources of recruitment
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- General population
- General Population
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- Volunteer enrolment
- Participants from Existing Studies
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Number of Participants
- Number of Participants
- 1,700
- Number of Participants with Biological Samples
- 1,700
Data Collection Events
| # | Name | Description | Start | End |
|---|---|---|---|---|
| 0 |
MAP - Baseline
|
Baseline data collection event contains cognitive measures, medical history questions, blood pressure, neuro exam, and a visit by the clinician. The Medical history questions bridge the period ... |
1997-12 | 2013-12 |
| 1 |
MAP - Annual Follow-up visit
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The window for the annual follow up visit is 9 – 16 months from previous visit. Annual follow up data collection event contains cognitive measures, medical history questions, blood pressure, ... |
1998-11 | 2013-12 |
Classifications
- Socio-demographic and economic characteristics
- Lifestyle and behaviours
- Birth, pregnancy and reproductive health history
- Perception of health, quality of life, development and functional limitations
- Diseases
- Symptoms and signs
- Medication and supplements
- Non-pharmacological interventions
- Health and community care services utilization
- Death
- Physical measures and assessments
- Laboratory measures
- Cognition, personality and psychological measures and assessments
- Life events, life plans, beliefs and values
- Preschool, school and work life
- Social environment and relationships
- Physical environment
- Administrative information
- Cognitive functioning
- Personality
- Psychological distress and emotions
- Other psychological measures and assessments
- Life events
- Beliefs and values
- Perception of health
- Quality of life
- Life course development
- Functional limitations
- Other perception of health, quality of life and functional limitation-related information
- Tobacco
- Alcohol
- Drugs
- Nutrition
- Breastfeeding
- Physical activity
- Sleep
- Sexual behaviours and orientation
- Technological devices
- Misbehaviour and criminality
- Other and unspecified lifestyle information
Socio-demographic and economic characteristics
Lifestyle and behaviours
Birth, pregnancy and reproductive health history
Perception of health, quality of life, development and functional limitations
Diseases
Symptoms and signs
Medication and supplements
Non-pharmacological interventions
Health and community care services utilization
Death
Physical measures and assessments
Cognition, personality and psychological measures and assessments
Life events, life plans, beliefs and values
Preschool, school and work life
Social environment and relationships
Administrative information
Cognitive functioning
Personality
Psychological distress and emotions
Beliefs and values
Quality of life
Functional limitations
Sleep