Glucose metabolism in children and adolescents: Population-based reference values and comparisons to children and adolescents enrolled in obesity treatment
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Glucose metabolism in children and adolescents : Population-based reference values and comparisons to children and adolescents enrolled in obesity treatment. / Frithioff-Bøjsøe, Christine; Lund, Morten A V; Kloppenborg, Julie T; Nielsen, Tenna T H; Fonvig, Cilius E; Lausten-Thomsen, Ulrik; Hedley, Paula L; Hansen, Tina; Pedersen, Oluf B; Christiansen, Michael; Baker, Jennifer L; Hansen, Torben; Holm, Jens-Christian.
I: Pediatric Diabetes, Bind 20, Nr. 5, 2019, s. 538-548.Publikation: Bidrag til tidsskrift › Tidsskriftartikel › Forskning › fagfællebedømt
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TY - JOUR
T1 - Glucose metabolism in children and adolescents
T2 - Population-based reference values and comparisons to children and adolescents enrolled in obesity treatment
AU - Frithioff-Bøjsøe, Christine
AU - Lund, Morten A V
AU - Kloppenborg, Julie T
AU - Nielsen, Tenna T H
AU - Fonvig, Cilius E
AU - Lausten-Thomsen, Ulrik
AU - Hedley, Paula L
AU - Hansen, Tina
AU - Pedersen, Oluf B
AU - Christiansen, Michael
AU - Baker, Jennifer L
AU - Hansen, Torben
AU - Holm, Jens-Christian
N1 - © 2019 John Wiley & Sons A/S. Published by John Wiley & Sons Ltd.
PY - 2019
Y1 - 2019
N2 - BACKGROUND: Alterations in glucose metabolism that lead to the development of metabolic and cardiovascular disease may begin already in childhood.OBJECTIVE: This study aims to generate pediatric age and sex-specific reference values for fasting concentrations of glucose, hemoglobin A1c (HbA1c), insulin, C-peptide, and homeostasis model assessment: insulin resistance (HOMA-IR) in Danish/North-European white children and adolescents from a population-based cohort and to compare values from children and adolescents with overweight/obesity with this reference.METHODS: The population- and obesity clinic-based cohorts consisted of 2451 and 1935 children and adolescents between 6 and 18 years of age. Anthropometric measurements and blood samples were obtained and percentile curves were calculated.RESULTS: In the population-based cohort, glucose, insulin, and HOMA-IR values increased before the expected onset of puberty (P < .05). Thereafter, all variables decreased in girls (P < .05) and HbA1c decreased in boys (P < .05). Concentrations of all measured markers of glucose metabolism were higher in the obesity clinic-based cohort than the population-based cohort (both sexes P < .001). Specifically, insulin and HOMA-IR continued to increase to 18 years in the clinic-based cohort, particularly among boys.CONCLUSIONS: Fasting glucose, insulin, and HOMA-IR change during childhood, making pediatric reference values essential for timely identification of derangements in glucose metabolism. Children and adolescents with obesity exhibit increased concentrations of these biomarkers.
AB - BACKGROUND: Alterations in glucose metabolism that lead to the development of metabolic and cardiovascular disease may begin already in childhood.OBJECTIVE: This study aims to generate pediatric age and sex-specific reference values for fasting concentrations of glucose, hemoglobin A1c (HbA1c), insulin, C-peptide, and homeostasis model assessment: insulin resistance (HOMA-IR) in Danish/North-European white children and adolescents from a population-based cohort and to compare values from children and adolescents with overweight/obesity with this reference.METHODS: The population- and obesity clinic-based cohorts consisted of 2451 and 1935 children and adolescents between 6 and 18 years of age. Anthropometric measurements and blood samples were obtained and percentile curves were calculated.RESULTS: In the population-based cohort, glucose, insulin, and HOMA-IR values increased before the expected onset of puberty (P < .05). Thereafter, all variables decreased in girls (P < .05) and HbA1c decreased in boys (P < .05). Concentrations of all measured markers of glucose metabolism were higher in the obesity clinic-based cohort than the population-based cohort (both sexes P < .001). Specifically, insulin and HOMA-IR continued to increase to 18 years in the clinic-based cohort, particularly among boys.CONCLUSIONS: Fasting glucose, insulin, and HOMA-IR change during childhood, making pediatric reference values essential for timely identification of derangements in glucose metabolism. Children and adolescents with obesity exhibit increased concentrations of these biomarkers.
U2 - 10.1111/pedi.12859
DO - 10.1111/pedi.12859
M3 - Journal article
C2 - 31074070
VL - 20
SP - 538
EP - 548
JO - Pediatric Diabetes
JF - Pediatric Diabetes
SN - 1399-543X
IS - 5
ER -
ID: 224552000