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Grant: Collaborative Health Research Projects (NSERC partnered)

University of Alberta

$396,500.00

Discovery of biomarkers of alzheimer's disease using comprehensive and quantitative metabolomics

FY 2011-12

Summary
"Currently 1 out of 11 Canadians suffers from some form of dementia. Alzheimer's disease (AD) is the leading form of dementia. An AD diagnosis can only be made through a lengthy and expensive process involving in the systematic elimination of other possible causes of cognitive impairment. While diagnostic accuracy of AD can be 90%, it is often made in the later disease stages where irreversible brain damage has already occurred. There is no cure for AD. Developing drugs for treating the disease is hindered by the lack of definitive chemical biomarkers that can be used for monitoring the disease progression, particularly in the earlier stages of AD. Thus, finding sensitive biomarkers for the early diagnosis or detection of AD is critical for managing and treating this devastating disease. While several proteins have been proposed as potential AD biomarkers, none has shown good specificity or sensitivity in clinical applications. The objective of this project is to apply newly developed mass spectrometry-based quantitative metabolomic techniques to search for small molecule biomarkers of AD. Our hypothesis is that in the early stages of AD, certain metabolic changes must be occurring in the brain and that by monitoring one or more key metabolites involved in these metabolic processes it may be possible to diagnose early-stage AD. To increase the likelihood of discovering specific AD biomarkers, we propose to apply state-of-the-art tools to comprehensively profile the metabolomes of urine, blood and cerebrospinal fluid (CSF) from AD patients. We will work with DynaLIFE Inc., a clinical diagnosis laboratory in Edmonton, to extent this study to validate the sensitivity and specificity of these biomarkers for diagnosis of AD. The anticipated results from this research include (1) verified (and validated in a small scale study) biomarkers for the early diagnosis of AD and (2) robust and inexpensive analytical methods for detecting these biomarkers. We believe that, if successful, this work could transform the management and treatment of AD and produce significant benefits to Canadians and the Canadian health care system."
Program
Collaborative Health Research Projects (NSERC partnered)
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
249355
Name
Li Liang
Region
Alberta
Country
Canada
Orgtype
Institution Paid; Research Institution
Partnername
Natural Sciences and Engineering Research Council of Canada (NSERC)
Prcname2
Collaborative Health Research Projects - NSERC Partnered
Projecttitle
Discovery of biomarkers of alzheimer's disease using comprehensive and quantitative metabolomics
Programtype2
Operating Grants
Orgnameinp2
University of Alberta
Cihramount2
$396,500
Cihrequipment2
$0
Programname2
Collaborative Health Research Projects (NSERC partnered)
Keyworddelim
Alzheimer'S Disease; Analytical Chemistry; Disease Biomarkers; Isotope Labeling; Mass Spectrometry; Metabolite Identification; Metabolome Profiling; Metabolomics; Quantitive Analysis
Abstract
"Currently 1 out of 11 Canadians suffers from some form of dementia. Alzheimer's disease (AD) is the leading form of dementia. An AD diagnosis can only be made through a lengthy and expensive process involving in the systematic elimination of other possible causes of cognitive impairment. While diagnostic accuracy of AD can be 90%, it is often made in the later disease stages where irreversible brain damage has already occurred. There is no cure for AD. Developing drugs for treating the disease is hindered by the lack of definitive chemical biomarkers that can be used for monitoring the disease progression, particularly in the earlier stages of AD. Thus, finding sensitive biomarkers for the early diagnosis or detection of AD is critical for managing and treating this devastating disease. While several proteins have been proposed as potential AD biomarkers, none has shown good specificity or sensitivity in clinical applications. The objective of this project is to apply newly developed mass spectrometry-based quantitative metabolomic techniques to search for small molecule biomarkers of AD. Our hypothesis is that in the early stages of AD, certain metabolic changes must be occurring in the brain and that by monitoring one or more key metabolites involved in these metabolic processes it may be possible to diagnose early-stage AD. To increase the likelihood of discovering specific AD biomarkers, we propose to apply state-of-the-art tools to comprehensively profile the metabolomes of urine, blood and cerebrospinal fluid (CSF) from AD patients. We will work with DynaLIFE Inc., a clinical diagnosis laboratory in Edmonton, to extent this study to validate the sensitivity and specificity of these biomarkers for diagnosis of AD. The anticipated results from this research include (1) verified (and validated in a small scale study) biomarkers for the early diagnosis of AD and (2) robust and inexpensive analytical methods for detecting these biomarkers. We believe that, if successful, this work could transform the management and treatment of AD and produce significant benefits to Canadians and the Canadian health care system."
Competitiondate
201110
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Li, Liang
Approvedterm
3 ans 0 mois
Cihrcontribution2
Institute of Aging~ $198,000~ $0~Knowledge Translation Branch~ $198,500~ $0~