AI4AD (Artificial Intelligence for Alzheimer’s Disease): Ultrascale Machine Learning to Empower Discovery in Alzheimer’s Disease Biobanks
- PI
- Crane, Paul
- DAR ID
- 10319
- Initial Approval Date
- July 16, 2021
- Current DAR Status
- Expired
- PI Institution
- University of Washington
- PI Institution Country
- United States
- PI Institution Type
- Non-Profit
Requested Datasets (1)
Research Use Statement
The AI4AD (Artificial Intelligence for Alzheimer’s Disease) Initiative aims to create and develop advanced AI methods, and apply them to genomic, imaging and cognitive data, in order to 1) identify AD genotypes and endophenotypes that dissect AD’s heterogeneity; 2) relate said genotypes and endophenotypes with clinical progression in pre-dementia patients; 3) identify novel treatment targets for AD by analyzing whole genome and associated phenotypic data. The goals of this multisite initiative (Paul Thompson, USC; Christos Davatzikos, Li Shen, Penn; Andy Saykin, IU; Heng Huang, Pitt, Paul Crane, UW; Adam Brickman, Columbia; Tim Hohman, Vanderbilt; Guyngah Jun, BU; Duygu Tosun, UCSF; Alexander Zaranek, Curii) leverage the promise of machine learning (ML) to contribute to precision diagnostics, prognostication, and targeted and novel treatments.
We will develop ML and deep learning methods to apply to large scale biobanks of whole genome sequences (WGS), neuroimaging, cognitive, and clinical data, aiming to discover new genomic features that influence biological processes of AD. We will apply methods of genome representation and tiling to WGS repositories to create inputs for AI methods.
We will develop novel, interpretable, biological knowledge guided deep learning methods to discover genomic motifs associated with AD, AD risk, and biological processes of AD as defined by NIA-AA criteria. To quantify subtypes and disentangle biological processes of AD, we will apply computational methods to multimodal MRI and amyloid- and tau-sensitive PET to stratify and subtype patient groups; novel imaging genomics methods will detect genomic markers and pathways that modulate the developing pathology as detected in the images, and that predict future clinical decline or resilience. We hypothesize that advanced deep learning methods combined with whole genome data will outperform traditional methods and GWAS for predicting AD onset and progression, and will assist with disease subtyping and discovering treatable targets in the genome. A team will rank and repurpose existing and identify novel drugs and targets in the genome based on the discovered genetic motifs affecting AD.
We will develop ML and deep learning methods to apply to large scale biobanks of whole genome sequences (WGS), neuroimaging, cognitive, and clinical data, aiming to discover new genomic features that influence biological processes of AD. We will apply methods of genome representation and tiling to WGS repositories to create inputs for AI methods.
We will develop novel, interpretable, biological knowledge guided deep learning methods to discover genomic motifs associated with AD, AD risk, and biological processes of AD as defined by NIA-AA criteria. To quantify subtypes and disentangle biological processes of AD, we will apply computational methods to multimodal MRI and amyloid- and tau-sensitive PET to stratify and subtype patient groups; novel imaging genomics methods will detect genomic markers and pathways that modulate the developing pathology as detected in the images, and that predict future clinical decline or resilience. We hypothesize that advanced deep learning methods combined with whole genome data will outperform traditional methods and GWAS for predicting AD onset and progression, and will assist with disease subtyping and discovering treatable targets in the genome. A team will rank and repurpose existing and identify novel drugs and targets in the genome based on the discovered genetic motifs affecting AD.
Non-Technical Summary
The AI4AD (Artificial Intelligence for Alzheimer’s Disease) Initiative aims to create and develop advanced AI methods, and apply them to extensive and rich genomic, imaging and cognitive data, in order to 1) identify genotypes and endophenotypes of AD that dissect the heterogeneity of the disease; 2) relate these genotypes and endophenotypes with clinical progression, in pre-dementia patients; 3) identify novel treatment targets for AD, by analyzing whole genome and associated phenotypic data at a previously impossible scale. Collectively, the goals of this highly collaborative multi-site initiative leverage the promise of machine learning to contribute to precision diagnostics, prognostication, and targeted and novel treatments.
Reported Publications (3)
Publications shown are those reported by investigators through NIAGADS DAR reporting and renewal processes and may not represent a complete list of publications associated with the project.
- Alzheimer's disease heterogeneity explained by polygenic risk scores derived from brain transcriptomic profiles. Chung J, et al. Alzheimer's & dementia : the journal of the Alzheimer's Association. 2023. PMID: 37166019
- Deep learning-based identification of genetic variants: application to Alzheimer's disease classification. Jo T, et al. Briefings in bioinformatics. 2022. PMID: 35183061
- Identifying highly heritable brain amyloid phenotypes through mining Alzheimer's imaging and sequencing biobank data. Bao J, et al. Pacific Symposium on Biocomputing. Pacific Symposium on Biocomputing. 2022. PMID: 34890141