Grant: Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Centre for Addiction and Mental Health (Toronto)
$105,000.00
Phenotype and Genotype Data Reduction for Machine Learning Classifier in Alzheimer's Disease
FY 2015-16
Summary
Currently 500,000 Canadians suffer from Alzheimer's disease (AD) and the elderly are Canada's fastest growing demographic group. Within 20 years 1.1 million Canadians will suffer from AD, raising the cost from $15 billion to $153 billion, and the number of hours of informal support by family and support networks from 231 million to 756 million hours. Strategies that either delay the disease onset, the conversion from prodromal stages to full AD, or that prevent the disease altogether would have a significant effect on the Canadian and, eventually, worldwide healthcare systems and would confer significant savings to the costs detailed above.
Our goal is to develop a method that efficiently analyzes AD-specific measures of brain shape and volume alongside genetic data in order to identify relationships between them. The main obstacle to combining imaging and genetics data is the sheer volume of data available for analysis. To ameliorate this problem, we propose the utilization of an AD-risk gene network with heritable brain structure to classify diagnoses between healthy, mild cognitive impairment and AD individuals. Combining both refined genetic and phenotypic biomarkers will allow for early identification of individuals at high risk for AD which could result in the initiation of treatments that either delay or halt the progression of AD altogether.
We believe this is an innovative proposal that addresses the urgent need for the discovery of novel biomarkers. This application combines a number of cutting edge technologies in a new way to identify genetic markers that identify individuals at high risk of AD before the onset of the disease. This proposal will have tremendous impact on health care systems in terms of burden and money saved, on the lives of community and family caregivers, and the patients themselves.
Department
Program
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Location
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
347947
Name
Patel Sejal
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Biomedical
Prcname2
Doctoral Research Awards - A
Projecttitle
Phenotype and Genotype Data Reduction for Machine Learning Classifier in Alzheimer's Disease
Programtype2
Studentship Programs
Orgnameinp2
Centre for Addiction and Mental Health (Toronto)
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Award - Frederick Banting and Charles Best Canada Graduate Scholarships
Keyworddelim
Alzheimer'S Disease; Bioinformatics; Gene Ontology; Genetics; Heritability Analysis; Machine Learning; Statistical Genetics; Structural Magnetic Resonance Imaging
Abstract
Currently 500,000 Canadians suffer from Alzheimer's disease (AD) and the elderly are Canada's fastest growing demographic group. Within 20 years 1.1 million Canadians will suffer from AD, raising the cost from $15 billion to $153 billion, and the number of hours of informal support by family and support networks from 231 million to 756 million hours. Strategies that either delay the disease onset, the conversion from prodromal stages to full AD, or that prevent the disease altogether would have a significant effect on the Canadian and, eventually, worldwide healthcare systems and would confer significant savings to the costs detailed above.
Our goal is to develop a method that efficiently analyzes AD-specific measures of brain shape and volume alongside genetic data in order to identify relationships between them. The main obstacle to combining imaging and genetics data is the sheer volume of data available for analysis. To ameliorate this problem, we propose the utilization of an AD-risk gene network with heritable brain structure to classify diagnoses between healthy, mild cognitive impairment and AD individuals. Combining both refined genetic and phenotypic biomarkers will allow for early identification of individuals at high risk for AD which could result in the initiation of treatments that either delay or halt the progression of AD altogether.
We believe this is an innovative proposal that addresses the urgent need for the discovery of novel biomarkers. This application combines a number of cutting edge technologies in a new way to identify genetic markers that identify individuals at high risk of AD before the onset of the disease. This proposal will have tremendous impact on health care systems in terms of burden and money saved, on the lives of community and family caregivers, and the patients themselves.
Competitiondate
201510
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Patel, Sejal
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~