An estimated 4 to 5 million Americans are living with Alzheimer's disease (AD), the most common form of dementia. This number could rise to 16 million by 2050. With the rapid increase in dementia cases due to an aging population structure there is an urgent need to identify opportunities for preventing or delaying its onset. We propose to test the hypothesis that protective socioeconomic, work and policy environments moderate the genetic risk for dementia and cognitive decline. Identifying modifiable aspects of the environment could provide means to prevent, or slow down, cognitive aging and AD. Few studies, however, have explored such gene-by-environment (GxE) interplay in AD and cognitive impairment. In addition, to our knowledge, no studies have yet attempted to address causality underlying GxE interplay in cognition or model its dynamic nature. Using significant and replicated results from existing genome-wide association studies (GWAS), we will create measures of genetic risk to examine our hypothesis. We will evaluate how GxE interplay evolves over the lifecycle, identify modifiable characteristics of the environment, establish the direction of causality and, when possible, investigate mechanisms that give rise to GxE interplay. We will use data from the Health and Retirement Study (HRS), the English Longitudinal Study of Ageing (ELSA), the Wisconsin Longitudinal Survey (WLS), and the UK Biobank (UKB). These studies are ideal for our purposes because of their large sample sizes, genetic and well-defined life-course cognition and socioeconomic data. The proposed research is innovative in its integrative approach, combining complimentary methods from genetics, epidemiology and social science. Our approach consists of descriptive analyses to explore associations for different measures of genetic risk, environments and stages of life (to explore critical phases;
aim 1); exploitation of natural experiments to address environmental causation (aim 2); and estimation of a structural life-course model to better understand GxE interplay, make predictions and evaluate intervention alternatives (aim 3). Combined, we anticipate these methods will provide important insights into the nature of genetic risk and the mechanisms at play in cognitive decline, and point to potential modifiable aspects of the socioeconomic, work and policy environment through an understanding of mechanisms and causality. To the best of our knowledge, our proposed research is unique in addressing causality, modeling life-course dynamics and adopting a structural approach. As a secondary aim of this project, harmonized genetic scores for cognitive function and Alzheimer's disease will be made publicly available for each of the four population studies as researcher-created data to enable replication and comparisons across studies.

Public Health Relevance

With the rising prevalence of dementia there is an urgent need to identify opportunities for preventing or delaying its onset. This project aims to use significant and replicated results from existing genome-wide association studies to develop measures of genetic risk and to examine whether protective socioeconomic, work and policy environments moderate the effect of genes on the development of dementia and cognitive decline in later life. We will evaluate how such gene-by-environment (GxE) interplay evolves over the lifecycle, identify modifiable characteristics of the environment, establish the direction of causality and, when possible, investigate mechanisms that give rise to GxE interplay.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Multi-Year Funded Research Project Grant (RF1)
Project #
3RF1AG055654-01A1S1
Application #
9780714
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Patmios, Georgeanne E
Project Start
2017-09-15
Project End
2022-06-30
Budget Start
2018-09-30
Budget End
2022-06-30
Support Year
1
Fiscal Year
2018
Total Cost
Indirect Cost
Name
University of Southern California
Department
Social Sciences
Type
Schools of Arts and Sciences
DUNS #
072933393
City
Los Angeles
State
CA
Country
United States
Zip Code
90089
Barcellos, Silvia H; Carvalho, Leandro S; Turley, Patrick (2018) Education can reduce health differences related to genetic risk of obesity. Proc Natl Acad Sci U S A 115:E9765-E9772
Ku?ma, El?bieta; Lourida, Ilianna; Moore, Sarah F et al. (2018) Stroke and dementia risk: A systematic review and meta-analysis. Alzheimers Dement 14:1416-1426
Ku?ma, El?bieta; Hannon, Eilis; Zhou, Ang et al. (2018) Which Risk Factors Causally Influence Dementia? A Systematic Review of Mendelian Randomization Studies. J Alzheimers Dis 64:181-193