Grant: CIHR-ICRH Travel Awards - General pool
University of British Columbia
$1,500.00
Early endothelial function activation by angiotensin II receptor blockers prevents vascular damage in a model of diabetes
EF 2023-24
Résumé
Type 1 diabetes (T1D) is an autoimmune disease typically diagnosed in childhood that has no cure. This chronic condition causes cells from the immune system to attack the pancreatic beta cells, destroying the body’s ability to produce insulin. Despite insulin replacement therapies, adults with T1D experience cardiovascular events more frequently and at an earlier age. We and others have reported that children diagnosed with T1D display cardiovascular risk factors like blood pressure abnormalities and indicators of vascular damage such as arterial stiffness. Therefore, we speculate that from diagnosis, T1D has begun to damage the vasculature, whereas early pharmacotherapy interventions with endothelial function enhancing drugs like angiotensin II receptor blockers may prevent long-term cardiovascular complications. Our research focuses on using a mouse model of T1D to characterize vascular damage from diabetes onset and exploring the use of early pharmacological interventions to prevent/reverse arterial stiffness and other long-term cardiovascular complications.
Programme
CIHR-ICRH Travel Awards - General pool
Bénéficiaire
Emplacement
British Columbia, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
493141
Name
Yuen Christopher
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Prcname2
Special Cases
Projecttitle
Early endothelial function activation by angiotensin II receptor blockers prevents vascular damage in a model of diabetes
Programtype2
Undefined
Orgnameinp2
University of British Columbia
Cihramount2
$1,500
Cihrequipment2
$0
Programname2
CIHR-ICRH Travel Awards - General pool
Keyworddelim
Type 1 Diabetes (T1d)
Abstract
Type 1 diabetes (T1D) is an autoimmune disease typically diagnosed in childhood that has no cure. This chronic condition causes cells from the immune system to attack the pancreatic beta cells, destroying the body’s ability to produce insulin. Despite insulin replacement therapies, adults with T1D experience cardiovascular events more frequently and at an earlier age. We and others have reported that children diagnosed with T1D display cardiovascular risk factors like blood pressure abnormalities and indicators of vascular damage such as arterial stiffness. Therefore, we speculate that from diagnosis, T1D has begun to damage the vasculature, whereas early pharmacotherapy interventions with endothelial function enhancing drugs like angiotensin II receptor blockers may prevent long-term cardiovascular complications. Our research focuses on using a mouse model of T1D to characterize vascular damage from diabetes onset and exploring the use of early pharmacological interventions to prevent/reverse arterial stiffness and other long-term cardiovascular complications.
Competitiondate
202309
Approvedterm2
1 yr 0 mth
Pinamesdelim
Yuen, Christopher
Approvedterm
1 an 0 mois
Cihrcontribution2
~ $1,500~ $0~