TY - JOUR
T1 - Adult-based genetic risk scores for insulin resistance associate with cardiometabolic traits in children and adolescents
AU - Suleman, Sufyan
AU - Huang, Yun
AU - Jensen, Rasmus Tanderup
AU - Poggi, Axel Illeris
AU - Christensen, Sara Bech
AU - Fraulund, Maria Martens
AU - Anderson, Louise Vølund
AU - Stinson, Sara Elizabeth
AU - Fonvig, Cilius Esmann
AU - Pedersen, Oluf
AU - Holm, Jens-Christian
AU - Hansen, Torben
AU - Grarup, Niels
N1 - © The Author(s) 2024. Published by Oxford University Press on behalf of the Endocrine Society.
PY - 2025/8/7
Y1 - 2025/8/7
N2 - CONTEXT: Insulin resistance (IR) is a key factor in the development of cardiometabolic diseases. While genetic risk scores (GRSs) for IR have been developed and validated in adult populations, it is unclear if they can be used for risk assessment in youth.OBJECTIVE: Our objective was to investigate whether adult-derived GRSs for IR associate with cardiometabolic traits in children and adolescents.METHODS: We studied a group of children and adolescents with obesity (n = 1680) and a group without obesity (n = 1804). We constructed 3 GRSs based on fasting (IR-GRS27), oral glucose tolerance test (IR-GRS8), and IR-related phenotypes (IR-GRS51) from previous genome-wide association studies. Using an additive genetic model, we calculated weighted GRSs and analyzed their associations with cardiometabolic traits using linear and logistic regression models.RESULTS: The IR-GRS27 was associated with higher serum concentrations of fasting insulin, C-peptide, triglycerides (TG), gamma-glutamyl transferase and alanine aminotransferase (ALT), and homeostatic model assessment of insulin resistance. The IR-GRS27 was furthermore associated with a higher prevalence of IR and ALT. IR-GRS51 was associated with higher TG and lower high-density lipoprotein cholesterol, while IR-GRS8 associated with lower total cholesterol, low-density lipoprotein cholesterol, and increased ALT. IR-GRS27 and IR-GRS8 were additionally associated with a higher prevalence of IR and steatotic liver disease, respectively.CONCLUSION: Adult-derived GRSs for IR are significantly associated with cardiometabolic traits in children and adolescents. If validated in independent study samples, our findings suggest the contribution of adult-based GRSs in assessing IR-related cardiometabolic risk in youth.
AB - CONTEXT: Insulin resistance (IR) is a key factor in the development of cardiometabolic diseases. While genetic risk scores (GRSs) for IR have been developed and validated in adult populations, it is unclear if they can be used for risk assessment in youth.OBJECTIVE: Our objective was to investigate whether adult-derived GRSs for IR associate with cardiometabolic traits in children and adolescents.METHODS: We studied a group of children and adolescents with obesity (n = 1680) and a group without obesity (n = 1804). We constructed 3 GRSs based on fasting (IR-GRS27), oral glucose tolerance test (IR-GRS8), and IR-related phenotypes (IR-GRS51) from previous genome-wide association studies. Using an additive genetic model, we calculated weighted GRSs and analyzed their associations with cardiometabolic traits using linear and logistic regression models.RESULTS: The IR-GRS27 was associated with higher serum concentrations of fasting insulin, C-peptide, triglycerides (TG), gamma-glutamyl transferase and alanine aminotransferase (ALT), and homeostatic model assessment of insulin resistance. The IR-GRS27 was furthermore associated with a higher prevalence of IR and ALT. IR-GRS51 was associated with higher TG and lower high-density lipoprotein cholesterol, while IR-GRS8 associated with lower total cholesterol, low-density lipoprotein cholesterol, and increased ALT. IR-GRS27 and IR-GRS8 were additionally associated with a higher prevalence of IR and steatotic liver disease, respectively.CONCLUSION: Adult-derived GRSs for IR are significantly associated with cardiometabolic traits in children and adolescents. If validated in independent study samples, our findings suggest the contribution of adult-based GRSs in assessing IR-related cardiometabolic risk in youth.
KW - Adolescent
KW - Adult
KW - Cardiometabolic Risk Factors
KW - Cardiovascular Diseases/genetics
KW - Child
KW - Female
KW - Genetic Predisposition to Disease
KW - Genetic Risk Score
KW - Genome-Wide Association Study
KW - Glucose Tolerance Test
KW - Humans
KW - Insulin Resistance/genetics
KW - Male
KW - Pediatric Obesity/genetics
KW - Phenotype
KW - Polymorphism, Single Nucleotide
KW - Risk Assessment
KW - Risk Factors
KW - Young Adult
UR - https://www.scopus.com/pages/publications/105013349706
U2 - 10.1210/clinem/dgae882
DO - 10.1210/clinem/dgae882
M3 - Journal article
C2 - 39690980
SN - 0021-972X
VL - 110
SP - 2645
EP - 2654
JO - The Journal of clinical endocrinology and metabolism
JF - The Journal of clinical endocrinology and metabolism
IS - 9
ER -