Grant: Project Grant
University of Saskatchewan
$952,425.00
PITX2-dependent mechanisms of atrial fibrillation pathogenesis
EF 2025-26
Résumé
Atrial fibrillation (AF) is the most common type of irregular heartbeat, affecting nearly one million Canadians and costing the healthcare system over $950 million each year. AF increases the risk of serious conditions like stroke, heart failure, and sudden cardiac death, yet current treatments often fall short. Both lifestyle factors and genetics play a role in AF, and recent research has uncovered many genetic variants linked to the disease. However, we still don't fully understand how these genes contribute to AF.
This project focuses on one key gene, PITX2, which helps regulate heart development and function. Using zebrafish and cell models, we will study how changes in PITX2 affect heart metabolism and lead to AF. Our research suggests that losing PITX2 function causes stress in heart cells, which may trigger arrhythmias. We aim to uncover the molecular pathways involved and explore whether targeting these pathways can slow or prevent AF. By combining advanced genetic tools and animal models, this work could lead to new insights into AF and pave the way for better treatments.
Programme
Project Grant
Bénéficiaire
Emplacement
Saskatchewan, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
534408
Name
Collins Michelle M
Region
Saskatchewan
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Cell Biology - Disease
Projecttitle
PITX2-dependent mechanisms of atrial fibrillation pathogenesis
Programtype2
Operating Grants
Orgnameinp2
University of Saskatchewan
Cihramount2
$952,425
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Cardiac Function; Cardiac Genetics; Cell Metabolism; Heart Development; Neonatal Rat Cardiomyocytes; Reactive Oxygen Species; Transcriptional Regulation; Zebrafish
Abstract
Atrial fibrillation (AF) is the most common type of irregular heartbeat, affecting nearly one million Canadians and costing the healthcare system over $950 million each year. AF increases the risk of serious conditions like stroke, heart failure, and sudden cardiac death, yet current treatments often fall short. Both lifestyle factors and genetics play a role in AF, and recent research has uncovered many genetic variants linked to the disease. However, we still don't fully understand how these genes contribute to AF.
This project focuses on one key gene, PITX2, which helps regulate heart development and function. Using zebrafish and cell models, we will study how changes in PITX2 affect heart metabolism and lead to AF. Our research suggests that losing PITX2 function causes stress in heart cells, which may trigger arrhythmias. We aim to uncover the molecular pathways involved and explore whether targeting these pathways can slow or prevent AF. By combining advanced genetic tools and animal models, this work could lead to new insights into AF and pave the way for better treatments.
Competitiondate
202509
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Collins, Michelle M
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $952,425~ $0~