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Grant: Collaborative Health Research Projects

University of Alberta

$95,500.00

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

FY 2013-14

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, toextent 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
Location
Alberta, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
414490-2012
Name nom
Li, Liang
Department département
Chemistry
Organization id
9
Institution établissement
University of Alberta
Province en
Alberta
Province fr
Alberta
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2013
Competition year année de concours
2012
Award amount
95500
Program id
CHRPJ
Program name en
Collaborative Health Research Projects
Program name fr
Projets de recherche concertée sur la santé
Group en
Discovery grants programs
Group fr
Programmes de subventions à la découverte
Committee code
360
Committee name en
Collaborative Health Research Projects Selection Panel
Committee name fr
Comité de sélection de projets de recherche concertée sur la santé
Area of application code
1101
Area of application group en
Health, education and social services
Area of application group fr
Santé publique, éducation et services sociaux
Area of application en
Human health (including medically-related psychological research)
Area of application fr
Santé publique (y compris recherche psychologique liée à la médecine)
Research subject code
3505
Research subject group en
Analytical chemistry
Research subject group fr
Chimie analytique
Research subject en
Analytical spectroscopy
Research subject fr
Spectroscopie analytique
Partie
2 & 3
Nb partie
3
Application title
Discovery of biomarkers of alzheimer's disease using comprehensive and quantitative metabolomics
Keyword
NSERC
Application 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, toextent 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.
University of Alberta - $95,500 Grant (2013-14) | Canada Spends