Canada Spends Logo

Explore our Budget 2026 analysis

Grant: Collaborative Health Research Projects

University of Waterloo

$154,089.00

Novel Diagnostic Methods for Imaging Amyloid Beta in the eye in association with alzheimer's disease

FY 2013-14

Summary
There is no cure and no early detection method broadly available for Alzheimer's disease (AD). Definite diagnosis is only after death. AD has a large negative impact on individual health and an enormous cost to society. Early diagnosis and improved disease tracking lead to earlier and better treatment. Amyloid beta forms deposits in the brain early in AD. We will develop a simpler method to image amyloid beta deposits in the living neural tissue at the back of the eye. Campbell's group has shown that these deposits should be large enough to be detected in images of the eye. They could then be used to diagnose and monitor the worsening stages of AD. We will explore the association between amyloid beta in the retina and the severity of AD. Amyloid beta deposits in retinas will be assessed after death. We will characterize the location, density, size and shape of retinal deposits. In a separate UBC study, the stage of AD will be measured in the clinic before death. Theirbrains are being imaged using PET and MRI scans. In addition, markers of AD in their blood and spinal fluid are measured. Characteristics of the retinal deposits will be compared with the stage of AD assessed by all the other measures. The living brains and retinas of a mouse model of AD will be imaged as they develop AD and after death. The time of appearance and characteristics of the amyloid beta deposits in the retinas and brains will be compared. Raman spectroscopy will be investigated as a noninvasive detection method of amyloid beta deposits in the retina. From these studies, we will understand the relationship between amyloid beta deposits in the retina and the severity of AD. We will then optimize the design of a novel system which will aid the diagnosis of Alzheimer disease by imaging the living retina. From the mouse model of AD, we will collect preliminary data on the performance of the system. The eye provides a clear view of neural tissue. Diagnosis of AD via this new imaging technology will be less expensive and more accessible to patients than current brain imaging methods.
Program
Collaborative Health Research Projects
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
NSERC's Awards Data

As published

Application id
413950-2012
Name nom
Campbell, Melanie
Department département
Physics and Astronomy
Organization id
33
Institution établissement
University of Waterloo
Province en
Ontario
Province fr
Ontario
Country en
CANADA
Country fr
CANADA
Fiscal year exercice financier
2013
Competition year année de concours
2012
Award amount
154089
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
1211
Area of application group en
Advancement of knowledge
Area of application group fr
Avancement des connaissances
Area of application en
Medical and health sciences
Area of application fr
Sciences médicales et de la santé
Research subject code
3114
Research subject group en
Physics
Research subject group fr
Physique
Research subject en
Biological and Medical Physics
Research subject fr
Physique biologique et médicale
Partie
2 & 3
Nb partie
3
Application title
Novel Diagnostic Methods for Imaging Amyloid Beta in the eye in association with alzheimer's disease
Keyword
NSERC
Application summary
There is no cure and no early detection method broadly available for Alzheimer's disease (AD). Definite diagnosis is only after death. AD has a large negative impact on individual health and an enormous cost to society. Early diagnosis and improved disease tracking lead to earlier and better treatment. Amyloid beta forms deposits in the brain early in AD. We will develop a simpler method to image amyloid beta deposits in the living neural tissue at the back of the eye. Campbell's group has shown that these deposits should be large enough to be detected in images of the eye. They could then be used to diagnose and monitor the worsening stages of AD. We will explore the association between amyloid beta in the retina and the severity of AD. Amyloid beta deposits in retinas will be assessed after death. We will characterize the location, density, size and shape of retinal deposits. In a separate UBC study, the stage of AD will be measured in the clinic before death. Theirbrains are being imaged using PET and MRI scans. In addition, markers of AD in their blood and spinal fluid are measured. Characteristics of the retinal deposits will be compared with the stage of AD assessed by all the other measures. The living brains and retinas of a mouse model of AD will be imaged as they develop AD and after death. The time of appearance and characteristics of the amyloid beta deposits in the retinas and brains will be compared. Raman spectroscopy will be investigated as a noninvasive detection method of amyloid beta deposits in the retina. From these studies, we will understand the relationship between amyloid beta deposits in the retina and the severity of AD. We will then optimize the design of a novel system which will aid the diagnosis of Alzheimer disease by imaging the living retina. From the mouse model of AD, we will collect preliminary data on the performance of the system. The eye provides a clear view of neural tissue. Diagnosis of AD via this new imaging technology will be less expensive and more accessible to patients than current brain imaging methods.
University of Waterloo - $154,089 Grant (2013-14) | Canada Spends