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Grant: DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)

Ottawa Hospital Research Institute

$120,000.00

Role of Clonal Hematopoiesis in Ischemic Stroke following Pulmonary Embolism in Racialized Populations

EF 2025-26

Résumé
Pulmonary embolism (PE) is a potentially fatal blood clot in the lungs and one of the leading causes of cardiovascular death. Even after recovery, people who have experienced a PE face a higher risk of ischemic stroke, which occurs when a blood vessel in the brain becomes blocked, particularly as they age. However, the reasons why this risk persists remain unclear. Inflammaging, a slow and persistent inflammation that develops with age and damages blood vessels, and clonal hematopoiesis of indeterminate potential (CHIP), a condition in which blood stem cells acquire mutations that increase inflammation, may help explain this connection. CHIP affects about one in ten adults over the age of 60 and has been linked to both heart disease and blood clots. Yet most studies on CHIP and inflammation have focused on people of European ancestry, leaving major gaps in understanding how these processes influence risk in racially and ethnically diverse populations who already face a higher burden of cardiovascular disease. This project will integrate data from large international cohorts to examine how CHIP and inflammaging contribute to long-term risk of ischemic stroke among people from diverse backgrounds who have survived a PE. We will analyze genetic and blood-based markers together with information on health, lifestyle, and social factors to better understand how aging, inflammation, and social disadvantage interact to influence stroke risk. By understanding these connections, this research aims to identify CHIP as a biological marker that can help predict who remains most at risk and guide the development of personalized and equitable prevention strategies that support healthy aging.
Programme
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Emplacement
Ontario, Canada
Type de bénéficiaire
Other
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
559290
Name
Khan Hassan
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Genetics
Theme2
Clinical
Prcname2
DT1 (Biomedical and/or Clinical Research) CGRS Doctoral
Projecttitle
Role of Clonal Hematopoiesis in Ischemic Stroke following Pulmonary Embolism in Racialized Populations
Programtype2
Studentship Programs
Orgnameinp2
Ottawa Hospital Research Institute
Cihramount2
$120,000
Cihrequipment2
$0
Programname2
DRA : Canada Graduate Research Scholarship - Doctoral Program (CGRS D)
Keyworddelim
Clonal Hematopoiesis; Geroscience; Health Equity; Inflammaging; Ischemic Stroke; Precision Medicine; Pulmonary Embolism; Socio-Biological Pathways; Translational Genomics; Vascular Aging
Abstract
Pulmonary embolism (PE) is a potentially fatal blood clot in the lungs and one of the leading causes of cardiovascular death. Even after recovery, people who have experienced a PE face a higher risk of ischemic stroke, which occurs when a blood vessel in the brain becomes blocked, particularly as they age. However, the reasons why this risk persists remain unclear. Inflammaging, a slow and persistent inflammation that develops with age and damages blood vessels, and clonal hematopoiesis of indeterminate potential (CHIP), a condition in which blood stem cells acquire mutations that increase inflammation, may help explain this connection. CHIP affects about one in ten adults over the age of 60 and has been linked to both heart disease and blood clots. Yet most studies on CHIP and inflammation have focused on people of European ancestry, leaving major gaps in understanding how these processes influence risk in racially and ethnically diverse populations who already face a higher burden of cardiovascular disease. This project will integrate data from large international cohorts to examine how CHIP and inflammaging contribute to long-term risk of ischemic stroke among people from diverse backgrounds who have survived a PE. We will analyze genetic and blood-based markers together with information on health, lifestyle, and social factors to better understand how aging, inflammation, and social disadvantage interact to influence stroke risk. By understanding these connections, this research aims to identify CHIP as a biological marker that can help predict who remains most at risk and guide the development of personalized and equitable prevention strategies that support healthy aging.
Competitiondate
202511
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Khan, Hassan
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $120,000~ $0~