Canada Spends Logo

Explore our Budget 2026 analysis

Grant: Project Grant

York University (Toronto, Ontario)

$749,700.00

Uncovering the mechanisms of atrial fibrillation using lessons from the adverse atrial remodeling induced by intense exercise

FY 2016-17

Summary
Atrial fibrillation (AF) is the most common cardiac arrhythmia whose incidence is increased with age, heart disease and ironically exercise. While exercise is invariably beneficial for the lower ventricular heart chambers, individuals engaging in intense and prolonged endurance get AF with a risk that is similar to that seen in heart disease patients. We have compelling evidence that the mechanisms driving AF in exercised mice is similar to that seen in AF due to heart disease, also rising with age. Moreover, our mechanism allows the identification of drug targets for AF treatment. Thus, we will identify the molecular and cellular pathways leading to AF broadly in all conditions associated with this arrhythmia and also identify novel therapies for AF treatment.
Program
Project Grant
Location
Ontario, Canada
Type
Grant
Source
CIHR Funding Decisions Database

As published

Id
357677
Name
Backx Peter H
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Circulatory and Respiratory Health
Theme2
Biomedical
Prcname2
Project Grant Competition
Projecttitle
Uncovering the mechanisms of atrial fibrillation using lessons from the adverse atrial remodeling induced by intense exercise
Programtype2
Operating Grants
Orgnameinp2
York University (Toronto, Ontario)
Cihramount2
$749,700
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Aging; Arrhytmias; Atrial Fibrillation; Diabetes; Exercise; Heart Disease
Abstract
Atrial fibrillation (AF) is the most common cardiac arrhythmia whose incidence is increased with age, heart disease and ironically exercise. While exercise is invariably beneficial for the lower ventricular heart chambers, individuals engaging in intense and prolonged endurance get AF with a risk that is similar to that seen in heart disease patients. We have compelling evidence that the mechanisms driving AF in exercised mice is similar to that seen in AF due to heart disease, also rising with age. Moreover, our mechanism allows the identification of drug targets for AF treatment. Thus, we will identify the molecular and cellular pathways leading to AF broadly in all conditions associated with this arrhythmia and also identify novel therapies for AF treatment.
Competitiondate
201610
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Backx, Peter H
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $749,700~ $0~