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Grant: CIHR Fellowship

Direct Payment

$225,000.00

Decoding interindividual variability in glycemic responses to diet using artificial intelligence (AI) models

EF 2024-25

Résumé
High fasting blood glucose (FG) doubles the risk of death from heart disease. A healthy diet can lower FG, but people are affected differently even after eating the same foods. This variation among people shows that "one size fits all" dietary guidelines may not be the best; there is a need for personalized nutrition. Factors like the gut microbiome, genetics, age, and lifestyle may influence different FG responses to diet, but how this happens is unclear. The relationship between diet and FG levels is inconsistent, because of limited data, small and similar samples, single time-point studies that ignore the time and age effect, and methods that do not capture complex interactions between different variables. My proposed research aims to address these issues by using data measured in over 10,000 adults in the "Nutrition for Precision Health" (United States) cohort and 13,000 children in the "Applied Research Group for Kids!" (Canada) cohort. Both datasets include multiple measures over time of FG and other blood markers, diet, gut microbiome, metabolomics, genetics, and over 2,000 lifestyle and environmental factors. Crucially, I will use advanced artificial intelligence (AI) methods to dig deeper into the complex interactions between these factors and FG levels, while examining how these relationships vary across different populations and age groups. Using advanced AI techniques, this project will integrate complex data and provide a deeper understanding of the reasons why we see variation in FG responses to diet. I will identify patterns and predictors of FG responses with greater precision for the first time in both children and adults. Using cutting-edge data analysis and big datasets, this project will inform personalized nutrition guidelines to lower FG levels based on each individual's needs and optimize disease prevention and treatment.
Programme
CIHR Fellowship
Bénéficiaire
Emplacement
New York, United States of America
Type
Grant
Source
CIHR Funding Decisions Database

Tel que publié

Id
512912
Name
Massara Paraskevi
Region
New York
Country
United States of America
Orgtype
Research Institution
Instname2
Nutrition, Metabolism and Diabetes
Theme2
Clinical
Prcname2
Health Research Training B - HP
Projecttitle
Decoding interindividual variability in glycemic responses to diet using artificial intelligence (AI) models
Programtype2
Fellowship Programs
Orgnameinp2
Direct Payment
Cihramount2
$225,000
Cihrequipment2
$0
Programname2
CIHR Fellowship
Keyworddelim
Artificial Intelligence; Blood Glucose; Data Science; Gut Microbiome; Longitudinal Analysis; Metabolic Health; Personalized Medicine; Population Health; Precision Nutrition
Abstract
High fasting blood glucose (FG) doubles the risk of death from heart disease. A healthy diet can lower FG, but people are affected differently even after eating the same foods. This variation among people shows that "one size fits all" dietary guidelines may not be the best; there is a need for personalized nutrition. Factors like the gut microbiome, genetics, age, and lifestyle may influence different FG responses to diet, but how this happens is unclear. The relationship between diet and FG levels is inconsistent, because of limited data, small and similar samples, single time-point studies that ignore the time and age effect, and methods that do not capture complex interactions between different variables. My proposed research aims to address these issues by using data measured in over 10,000 adults in the "Nutrition for Precision Health" (United States) cohort and 13,000 children in the "Applied Research Group for Kids!" (Canada) cohort. Both datasets include multiple measures over time of FG and other blood markers, diet, gut microbiome, metabolomics, genetics, and over 2,000 lifestyle and environmental factors. Crucially, I will use advanced artificial intelligence (AI) methods to dig deeper into the complex interactions between these factors and FG levels, while examining how these relationships vary across different populations and age groups. Using advanced AI techniques, this project will integrate complex data and provide a deeper understanding of the reasons why we see variation in FG responses to diet. I will identify patterns and predictors of FG responses with greater precision for the first time in both children and adults. Using cutting-edge data analysis and big datasets, this project will inform personalized nutrition guidelines to lower FG levels based on each individual's needs and optimize disease prevention and treatment.
Competitiondate
202410
Approvedterm2
3 yrs 0 mth
Pinamesdelim
Massara, Paraskevi
Approvedterm
3 ans 0 mois
Cihrcontribution2
~ $225,000~ $0~