Grant: Team Grant: UK-Canada Diabetes Research Team Grants
University of British Columbia
$449,091.00
Bridging the gap to translation by understadning and preventing diabetic vascular complications using human organoid culture (MRC NPI: David Andrew Long)
FY 2019-20
Summary
Diabetes affects 3.0 Million Canadians. Globally 8.8% of the population is affected by this disease and this number is rising due to an aging population and increasing obesity. In Canada, the cost of treating new cases of diabetes diagnosed from 2012-22 is estimated at $15.4 Billion, while in the UK 10% of the NHS budget is spent on treating diabetes and complications associated with it, such as kidney disease, blindness, heart attacks, and stroke. These complications are often caused by changes in the blood vessels, therefore, strategies which protect or repair blood vessels may provide new treatments for diabetic patients. Laboratory studies on mice and cells have identified several molecules that can protect blood vessels, but moving these findings from laboratories to humans has been difficult. Dr. Penninger has recently developed a novel method to create artificial human blood vessels from human stem cells. When exposed to diabetic conditions in the laboratory or in mice, these blood vessels show the same changes and features as seen in the blood vessels of diabetic patients. These artificial blood vessels allow scientists to examine promising laboratory findings in a human-like environment before conducting clinical trials with human patients. In this project Dr. Penninger will work with a team of U.K-based scientists, Drs. David Long, Luigi Gnudi, and Karen Price to assess the potential of two previously identified molecules angiopoietin-2 and apelin to reverse changes caused by high blood sugar levels in these artificial human blood vessels. Additionally, the team will examine why some diabetic patients do not develop blood vessel related complications, using blood samples from diabetic patients with or without albumin protein in their urine. Excessive albumin in the urine of a diabetic patient is an indication of diabetic kidney disease. Their findings will ultimately lead to the discovery of new treatments for blood vessel complications in diabetes.
Department
Program
Team Grant: UK-Canada Diabetes Research Team Grants
Recipient
Location
British Columbia, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
410862
Name
Penninger Josef
Region
British Columbia
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Biomedical
Prcname2
UK-Canada Diabetes Research Team Grant
Projecttitle
Bridging the gap to translation by understadning and preventing diabetic vascular complications using human organoid culture (MRC NPI: David Andrew Long)
Programtype2
Operating Grants
Orgnameinp2
University of British Columbia
Cihramount2
$449,091
Cihrequipment2
$0
Programname2
Team Grant: UK-Canada Diabetes Research Team Grants
Keyworddelim
Albuminuria; Angiopoietin-2 Blockade; Apelin Blockade; Blood Vessel Damage Protective Factors; Blood Vessel Organoids; Diabetes; Diabetic Nephropathy; Diabetic Vasculopathy
Abstract
Diabetes affects 3.0 Million Canadians. Globally 8.8% of the population is affected by this disease and this number is rising due to an aging population and increasing obesity. In Canada, the cost of treating new cases of diabetes diagnosed from 2012-22 is estimated at $15.4 Billion, while in the UK 10% of the NHS budget is spent on treating diabetes and complications associated with it, such as kidney disease, blindness, heart attacks, and stroke. These complications are often caused by changes in the blood vessels, therefore, strategies which protect or repair blood vessels may provide new treatments for diabetic patients. Laboratory studies on mice and cells have identified several molecules that can protect blood vessels, but moving these findings from laboratories to humans has been difficult. Dr. Penninger has recently developed a novel method to create artificial human blood vessels from human stem cells. When exposed to diabetic conditions in the laboratory or in mice, these blood vessels show the same changes and features as seen in the blood vessels of diabetic patients. These artificial blood vessels allow scientists to examine promising laboratory findings in a human-like environment before conducting clinical trials with human patients. In this project Dr. Penninger will work with a team of U.K-based scientists, Drs. David Long, Luigi Gnudi, and Karen Price to assess the potential of two previously identified molecules angiopoietin-2 and apelin to reverse changes caused by high blood sugar levels in these artificial human blood vessels. Additionally, the team will examine why some diabetic patients do not develop blood vessel related complications, using blood samples from diabetic patients with or without albumin protein in their urine. Excessive albumin in the urine of a diabetic patient is an indication of diabetic kidney disease. Their findings will ultimately lead to the discovery of new treatments for blood vessel complications in diabetes.
Competitiondate
201909
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Penninger, Josef
Approvedterm
3 ans 0 mois
Cihrcontribution2
Inst of Nutr Metabolism &Diab~ $449,091~ $0~