Grant: Project Grant
Université de Sherbrooke
$1,197,226.00
Stimulating adipose tissue fatty acid disposal with low-dose, postprandial, intermittent niacin for the treatment of metabolic dysfunction-associated steatotic liver disease
EF 2023-24
Résumé
Metabolic dysfunction-associated steatotic liver disease (MASLD) affects up to one third of the adult population, strongly associates with obesity, type 2 diabetes (T2D) and cardiovascular diseases, and leads to liver inflammation and fibrosis (i.e., metabolic dysfunction-associated steatohepatitis - MASH). There is currently no approved treatment for MASLD/MASH. This disease is caused by excess storage of fat in the liver. This excess fat to the liver also contributes to liver insulin resistance and the development of T2D. Abnormal storage within the fat tissues of the fats that come from our food contributes to excess storage of fat in the liver, offering a possible explanation as to why obesity so often leads to T2D and MASLD/MASH. Using our unique medical imaging methods, we recently found that niacin, an old, safe and low-cost drug to reduce cholesterol and fat in the blood, administered after a meal leads to a 40% reduction of fat entering the liver, and drives fats from the food to be stored in the fat tissues. This may open up an entirely new treatment strategy for individuals living with MASLD/MASH. This new study therefore aims to demonstrate the effect of a 12-week treatment with niacin administered after the largest meal of the day on the storage of fats in fat tissues and the liver. We will also measure liver insulin resistance and inflammation in response to this treatment. Our study will include an equal number of women and men in order to be able to explore differences in results between both sexes. We recently made exciting technological additions to our state-of-the-art medical imaging methods and facilities to measure all features of fat tissue fatty acid metabolism. Our results may lead to a new therapy to help people living with MASLD/MASH, a poorly managed condition that may lead to severe complications such as T2D, cardiac diseases and liver failure.
Programme
Project Grant
Bénéficiaire
Emplacement
Quebec, Canada
Type de bénéficiaire
Academia
Type
Grant
Source
CIHR Funding Decisions Database
Tel que publié
Id
500326
Name
Carpentier André C
Region
Québec
Country
Canada
Orgtype
Institution Paid; Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Clinical
Prcname2
Diabetes, Obesity, Lipid & Lipoprotein Disorders
Projecttitle
Stimulating adipose tissue fatty acid disposal with low-dose, postprandial, intermittent niacin for the treatment of metabolic dysfunction-associated steatotic liver disease
Programtype2
Operating Grants
Orgnameinp2
Université de Sherbrooke
Cihramount2
$1,197,226
Cihrequipment2
$0
Programname2
Project Grant
Keyworddelim
Abdominal Obesity; Adipose Tissue Metabolism; Fatty Acid Metabolism; Hepatic Metabolism; Magnetic Resonance Imaging; Metabolic Dysfunction-Associated Steatotic Liver Disease; Molecular Imaging; Positron Emission Tomography; Tracer Methods; Type 2 Diabetes
Abstract
Metabolic dysfunction-associated steatotic liver disease (MASLD) affects up to one third of the adult population, strongly associates with obesity, type 2 diabetes (T2D) and cardiovascular diseases, and leads to liver inflammation and fibrosis (i.e., metabolic dysfunction-associated steatohepatitis - MASH). There is currently no approved treatment for MASLD/MASH. This disease is caused by excess storage of fat in the liver. This excess fat to the liver also contributes to liver insulin resistance and the development of T2D. Abnormal storage within the fat tissues of the fats that come from our food contributes to excess storage of fat in the liver, offering a possible explanation as to why obesity so often leads to T2D and MASLD/MASH. Using our unique medical imaging methods, we recently found that niacin, an old, safe and low-cost drug to reduce cholesterol and fat in the blood, administered after a meal leads to a 40% reduction of fat entering the liver, and drives fats from the food to be stored in the fat tissues. This may open up an entirely new treatment strategy for individuals living with MASLD/MASH. This new study therefore aims to demonstrate the effect of a 12-week treatment with niacin administered after the largest meal of the day on the storage of fats in fat tissues and the liver. We will also measure liver insulin resistance and inflammation in response to this treatment. Our study will include an equal number of women and men in order to be able to explore differences in results between both sexes. We recently made exciting technological additions to our state-of-the-art medical imaging methods and facilities to measure all features of fat tissue fatty acid metabolism. Our results may lead to a new therapy to help people living with MASLD/MASH, a poorly managed condition that may lead to severe complications such as T2D, cardiac diseases and liver failure.
Competitiondate
202403
Approvedterm2
5 yrs 0 mth
Pinamesdelim
Carpentier, André C
Approvedterm
5 ans 0 mois
Cihrcontribution2
~ $1,197,226~ $0~