Grant: Doctoral Research Award: Canada Graduate Scholarships
York University (Toronto, Ontario)
$105,000.00
Longitudinal Neurocognitive Outcomes and Trajectories of Brain Development in Pediatric Patients with Multiple Sclerosis and Relapsing Myelin Oligodendrocyte Glycoprotein (MOG) Disease
FY 2019-20
Summary
The immune system protects the body from intruders (e.g., viruses and bacteria). However, sometimes, healthy tissue might be accidentally mistaken for an intruder and become the target of immune system attack. This is associated with the onset of diseases such as multiple sclerosis (MS) and myelin oligodendrocyte glycoprotein (MOG) disease. Researchers recently confirmed that pediatric patients with relapsing MOG disease represent a distinct population from those with MS; previously, patients with relapsing MOG may have been misdiagnosed with MS.
MOG disease can either be relapsing or monophasic (i.e., a single demyelinating event), unlike pediatric MS which typically follows a relapsing course. MOG is produced exclusively in the brain and spinal cord. It is involved in the production of myelin, an insulating cover that permits electrical impulses to be conducted quickly along nerves for efficient communication between brain regions. Given that the myelin sheath is damaged in both MS and MOG disease, both conditions are called demyelinating diseases.
Pediatric demyelinating diseases are diagnosed when the first attack is experienced before age 18. We have studied pediatric MS and identified challenges with organizing information and processing speed, among other cognitive deficits. What remains unclear is whether pediatric patients with MS and relapsing MOG disease have comparable patterns of cognitive function. The objective of our study is to understand the cognitive profile of patients with relapsing MOG disease. We will compare patient groups as well as patients with relapsing MOG and matched healthy participants. We will then examine patterns of brain growth in pediatric patients with MS and relapsing MOG disease. We will also evaluate whether brain changes due to these pediatric demyelinating diseases are associated with poorer cognitive performance in both patient groups. Methods include computerized cognitive testing and magnetic-resonance imaging (MRI).
Department
Program
Doctoral Research Award: Canada Graduate Scholarships
Recipient
Location
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
416816
Name
Fabri Tracy L
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Neurosciences, Mental Health and Addiction
Theme2
Clinical
Prcname2
Doctoral Research Awards - B
Projecttitle
Longitudinal Neurocognitive Outcomes and Trajectories of Brain Development in Pediatric Patients with Multiple Sclerosis and Relapsing Myelin Oligodendrocyte Glycoprotein (MOG) Disease
Programtype2
Studentship Programs
Orgnameinp2
York University (Toronto, Ontario)
Cihramount2
$105,000
Cihrequipment2
$0
Programname2
Doctoral Research Award: Canada Graduate Scholarships
Keyworddelim
Brain Development; Computerized Neurocognitive Assessment; Magnetic Resonance Imaging (Mri); Neurocognitive Outcomes; Pediatric Demyelinating Disease; Pediatric Multiple Sclerosis; Relapsing Myelin Oligodendrocyte Glycoprotein Disease
Abstract
The immune system protects the body from intruders (e.g., viruses and bacteria). However, sometimes, healthy tissue might be accidentally mistaken for an intruder and become the target of immune system attack. This is associated with the onset of diseases such as multiple sclerosis (MS) and myelin oligodendrocyte glycoprotein (MOG) disease. Researchers recently confirmed that pediatric patients with relapsing MOG disease represent a distinct population from those with MS; previously, patients with relapsing MOG may have been misdiagnosed with MS.
MOG disease can either be relapsing or monophasic (i.e., a single demyelinating event), unlike pediatric MS which typically follows a relapsing course. MOG is produced exclusively in the brain and spinal cord. It is involved in the production of myelin, an insulating cover that permits electrical impulses to be conducted quickly along nerves for efficient communication between brain regions. Given that the myelin sheath is damaged in both MS and MOG disease, both conditions are called demyelinating diseases.
Pediatric demyelinating diseases are diagnosed when the first attack is experienced before age 18. We have studied pediatric MS and identified challenges with organizing information and processing speed, among other cognitive deficits. What remains unclear is whether pediatric patients with MS and relapsing MOG disease have comparable patterns of cognitive function. The objective of our study is to understand the cognitive profile of patients with relapsing MOG disease. We will compare patient groups as well as patients with relapsing MOG and matched healthy participants. We will then examine patterns of brain growth in pediatric patients with MS and relapsing MOG disease. We will also evaluate whether brain changes due to these pediatric demyelinating diseases are associated with poorer cognitive performance in both patient groups. Methods include computerized cognitive testing and magnetic-resonance imaging (MRI).
Competitiondate
201911
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Fabri, Tracy L
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $105,000~ $0~