Grant: Operating Grant
McMaster University
$327,582.00
Integration of genetic determinants of lipoprotein(a), concentration and isoform size in relation to risk of coronary heart disease in a multi-ethnic population
FY 2009-10
Summary
Heart disease is a leading cause of death in Canada. In addition to risk factors such as smoking and diabetes, increased fats and cholesterol in the blood can lead to narrowing and blockage of the blood vessels to the heart. These fats and cholesterol are carried in the blood in packages called lipoproteins. Increased amounts of one of these packages in the blood, called lipoprotein(a)[ Lp(a) ], is associated with increased risk of heart and blood vessel disease. However, the real importance of Lp(a) is not yet clear because people of differing genetic ancestry have varying amount and sizes of Lp(a). The size of Lp(a) is determined by our genes. The different sizes of Lp(a) make it difficult to measure in the blood. Another challenge is that smaller size Lp(a) packages lead to larger number of the Lp(a) packages in the blood. People can have their Lp(a) measured using different types of tests. The tests can either measure how much of the lipoprotein is in the blood, determine the Lp(a) gene type or look at the size of Lp(a). At the moment, we are not sure if there is one best test to use in all ethnic groups or if it is better to use a combination of tests. We plan to use 4 different laboratory techniques. One will measure the amount of Lp(a). The second will identify the genetic factors. The other two will determine the different sizes of Lp(a) in each blood sample. We will use blood samples from a very large international study (the INTERHEART study) which was designed to allow us to understand the factors that can be used to predict the risk of someone having a heart attack. The INTERHEART study involved more than 20,000 women and men, young and old, from 52 countries and many ethnic groups. The study we propose is the first to combine these 4 laboratory techniques in a large number of people from many ethnic groups to try to fully understand Lp(a) and its value in helping to predict the risk of developing heart and blood vessel disease.
Department
Program
Operating Grant
Recipient
Location
Ontario, Canada
Recipient Type
Academia
Type
Grant
Source
CIHR Funding Decisions Database
As published
Id
202205
Name
Paré Guillaume
Region
Ontario
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Clinical
Prcname2
Diabetes, Obesity, Lipid & Lipoprotein Disorders
Projecttitle
Integration of genetic determinants of lipoprotein(a), concentration and isoform size in relation to risk of coronary heart disease in a multi-ethnic population
Programtype2
Operating Grants
Orgnameinp2
McMaster University
Cihramount2
$327,582
Cihrequipment2
$0
Programname2
Operating Grant
Keyworddelim
Biomarker; Genetics; Lipoprotein(A); Lipoproteins; Myocardial Infarction; Population Health
Abstract
Heart disease is a leading cause of death in Canada. In addition to risk factors such as smoking and diabetes, increased fats and cholesterol in the blood can lead to narrowing and blockage of the blood vessels to the heart. These fats and cholesterol are carried in the blood in packages called lipoproteins. Increased amounts of one of these packages in the blood, called lipoprotein(a)[ Lp(a) ], is associated with increased risk of heart and blood vessel disease. However, the real importance of Lp(a) is not yet clear because people of differing genetic ancestry have varying amount and sizes of Lp(a). The size of Lp(a) is determined by our genes. The different sizes of Lp(a) make it difficult to measure in the blood. Another challenge is that smaller size Lp(a) packages lead to larger number of the Lp(a) packages in the blood. People can have their Lp(a) measured using different types of tests. The tests can either measure how much of the lipoprotein is in the blood, determine the Lp(a) gene type or look at the size of Lp(a). At the moment, we are not sure if there is one best test to use in all ethnic groups or if it is better to use a combination of tests. We plan to use 4 different laboratory techniques. One will measure the amount of Lp(a). The second will identify the genetic factors. The other two will determine the different sizes of Lp(a) in each blood sample. We will use blood samples from a very large international study (the INTERHEART study) which was designed to allow us to understand the factors that can be used to predict the risk of someone having a heart attack. The INTERHEART study involved more than 20,000 women and men, young and old, from 52 countries and many ethnic groups. The study we propose is the first to combine these 4 laboratory techniques in a large number of people from many ethnic groups to try to fully understand Lp(a) and its value in helping to predict the risk of developing heart and blood vessel disease.
Competitiondate
201003
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Paré, Guillaume
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $327,582~ $0~