Genetics of deep-learning-derived neuroimaging endophenotypes for Alzheimer's Disease (Parent grant)
University Of Texas Hlth Sci Ctr Houston, Houston TX
Investigators
Linked publications & trials
Abstract
Project Summary Alzheimerâs disease (AD) is characterized by the progressive impairment of cognitive and memory functions and is the most common form of dementia in the elderly. It affects 5.6 million Americans over the age of 65 and exacts tremendous and increasing demands on patients, caregivers, and healthcare resources, making this condition among the most significant public health problems of our time. Despite extensive studies, our understanding of the biology and pathophysiology of AD is still limited, hindering advances in the development of therapeutic and preventive strategies. Genetic studies of AD have successfully identified 40 novel loci but these explain only a fraction of the overall disease risk, suggesting opportunities for additional discoveries. Advanced neuroimaging is an essential part of current AD clinical and research investigations, which generally focus on relatively few imaging phenotypes developed by neuro- radiologists. However, there is a growing interest in exploiting the high-content information in large-scale, high dimensional multimodal neuroimaging data to identify novel AD biomarkers. Deep learning (DL) methods, an emerging area of machine learning research, uses raw images to derive optimal vector representations of imaging contents, which can be used as informative AD endophenotypes. The overall goal of the proposed supplement is to benchmark the AI algorithms we are developing on a standardized neuroimaging dataset. We will work on two topics: Predicting clinical decline (prognosis) from baseline T1-weighted brain MRI, and Discovery of genetic loci in whole- genome sequence data associated with brain MRI-derived endophenotypes. This is a collaboration with the other two U01 awards to improve the rigor and reproducibility. We will make the software tools and results publicly available. This will positively impact the larger research community.
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