Genetic factors play an important role in the development of Alzheimer's disease. While much progress has been made in Alzheimer?s disease genetics, the role of noncoding variants is largely unknown. The noncoding genome covers ~98% of the human genome and includes elements that regulate when, where, and to what degree protein-coding genes (e.g. APOE) are transcribed. The objective of this proposal will be to focus specifically on the analysis of whole-genome sequencing studies of Alzheimer?s disease, in order to identify rare noncoding variants and characterize their role in Alzheimer?s disease pathogenesis. We will attain our objective via an innovative approach, combining whole-genome sequencing, epigenetic technologies and multi-layered phenotypic data such as imaging and biomarkers. This will lead to a unique combination of methodologies for the analysis of noncoding variants, allowing for absence of natural units (e.g. genes) for testing (Aim 1), integration of multi-layer information for enhancing power (Aim 2), and biologically meaningful interpretation of association signals (Aim 3). The proposed methods will be applied to a total of roughly 20,000 whole genomes unifying the Alzheimer's Disease Neuroimaging Initiative (ADNI), the Alzheimer's Disease Sequencing Project (ADSP), the Religious Orders Study and Memory and Aging Project (ROSMAP) and a newly established cohort, the Stanford Extreme Phenotypes in Alzheimer's Disease (StEP AD). We expect that the application of the proposed methods will significantly improve our understanding of the genetic architecture of Alzheimer's disease and, critically, provide a set of well-defined, novel targets for the development of genomic-driven medicine.

Public Health Relevance

The proposed research is relevant to public health because understanding noncoding sequence in the human genome could provide insights into Alzheimer?s disease and refined control of emerging genetic therapies. The proposed integrative analysis will identify rare noncoding variants and characterize their role in Alzheimer?s disease pathogenesis, which will facilitate future personalized medicine using genetic data to improve human health. Therefore, this proposal is relevant to the part of NIH?s mission that pertains to fostering fundamental creative discoveries, innovative research strategies, and their applications as a basis for ultimately protecting and improving health.

Agency
National Institute of Health (NIH)
Institute
National Institute on Aging (NIA)
Type
Research Project (R01)
Project #
5R01AG066206-02
Application #
10017852
Study Section
Special Emphasis Panel (ZRG1)
Program Officer
Miller, Marilyn
Project Start
2019-09-15
Project End
2024-05-31
Budget Start
2020-06-01
Budget End
2021-05-31
Support Year
2
Fiscal Year
2020
Total Cost
Indirect Cost
Name
Stanford University
Department
Neurology
Type
Schools of Medicine
DUNS #
009214214
City
Stanford
State
CA
Country
United States
Zip Code
94305