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Fetal Growth Trajectories and Measures of Insulin Resistance in Young Adults

CONTEXT: Events during gestation greatly influence the risk of cardiometabolic diseases including diabetes in offspring during later life. OBJECTIVE: This study aimed to investigate relationships between serial ultrasound-derived fetal growth trajectories and markers of insulin resistance in young a...

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Autores principales: Yadav, Ashish, Beilin, Lawrence J, Huang, Rae-Chi, Newnham, John P, White, Scott W, Mori, Trevor A
Formato: Online Artículo Texto
Lenguaje:English
Publicado: Oxford University Press 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656704/
https://www.ncbi.nlm.nih.gov/pubmed/37246587
http://dx.doi.org/10.1210/clinem/dgad292
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author Yadav, Ashish
Beilin, Lawrence J
Huang, Rae-Chi
Newnham, John P
White, Scott W
Mori, Trevor A
author_facet Yadav, Ashish
Beilin, Lawrence J
Huang, Rae-Chi
Newnham, John P
White, Scott W
Mori, Trevor A
author_sort Yadav, Ashish
collection PubMed
description CONTEXT: Events during gestation greatly influence the risk of cardiometabolic diseases including diabetes in offspring during later life. OBJECTIVE: This study aimed to investigate relationships between serial ultrasound-derived fetal growth trajectories and markers of insulin resistance in young adults in the Raine Study, an Australian pregnancy cohort. METHODS: Linear mixed modeling examined the relationship between fetal growth trajectory groups, constructed using serial ultrasound-based abdominal circumference (AC), femur length (FL), and head circumference (HC) from 1333 mother-fetal pairs, and offspring Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), as a marker of diabetes risk, at 20 (n = 414), 22 (n = 385), and 27 (n = 431) years. Analyses were adjusted for age, sex, ethnicity, socioeconomic status, adult lifestyle factors, and maternal factors during pregnancy. RESULTS: The study identified 7 AC, 5 FL, and 5 HC growth trajectory groups. Compared to the average-stable (reference) group, a low-falling AC growth trajectory (26%; P = .005) and 2 low HC growth trajectories (20%; P = .006% and 8%; P = .021) were associated with higher adult HOMA-IR. Trajectories representing a high-stable FL and a rising HC were associated with 12% (P = .002) and 9% (P = .021) lower adult HOMA-IR, respectively, compared to the reference group. CONCLUSION: Restricted fetal HC and AC from early pregnancy are associated with higher relative insulin resistance in the offspring during adulthood. These data strengthen our understanding of the importance of the intrauterine environment and its effect on the risk of predisposition to adult diabetes and related metabolic disorders.
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spelling pubmed-106567042023-01-29 Fetal Growth Trajectories and Measures of Insulin Resistance in Young Adults Yadav, Ashish Beilin, Lawrence J Huang, Rae-Chi Newnham, John P White, Scott W Mori, Trevor A J Clin Endocrinol Metab Clinical Research Article CONTEXT: Events during gestation greatly influence the risk of cardiometabolic diseases including diabetes in offspring during later life. OBJECTIVE: This study aimed to investigate relationships between serial ultrasound-derived fetal growth trajectories and markers of insulin resistance in young adults in the Raine Study, an Australian pregnancy cohort. METHODS: Linear mixed modeling examined the relationship between fetal growth trajectory groups, constructed using serial ultrasound-based abdominal circumference (AC), femur length (FL), and head circumference (HC) from 1333 mother-fetal pairs, and offspring Homeostatic Model Assessment of Insulin Resistance (HOMA-IR), as a marker of diabetes risk, at 20 (n = 414), 22 (n = 385), and 27 (n = 431) years. Analyses were adjusted for age, sex, ethnicity, socioeconomic status, adult lifestyle factors, and maternal factors during pregnancy. RESULTS: The study identified 7 AC, 5 FL, and 5 HC growth trajectory groups. Compared to the average-stable (reference) group, a low-falling AC growth trajectory (26%; P = .005) and 2 low HC growth trajectories (20%; P = .006% and 8%; P = .021) were associated with higher adult HOMA-IR. Trajectories representing a high-stable FL and a rising HC were associated with 12% (P = .002) and 9% (P = .021) lower adult HOMA-IR, respectively, compared to the reference group. CONCLUSION: Restricted fetal HC and AC from early pregnancy are associated with higher relative insulin resistance in the offspring during adulthood. These data strengthen our understanding of the importance of the intrauterine environment and its effect on the risk of predisposition to adult diabetes and related metabolic disorders. Oxford University Press 2023-01-29 /pmc/articles/PMC10656704/ /pubmed/37246587 http://dx.doi.org/10.1210/clinem/dgad292 Text en © The Author(s) 2023. Published by Oxford University Press on behalf of the Endocrine Society. https://creativecommons.org/licenses/by/4.0/This is an Open Access article distributed under the terms of the Creative Commons Attribution License (https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.
spellingShingle Clinical Research Article
Yadav, Ashish
Beilin, Lawrence J
Huang, Rae-Chi
Newnham, John P
White, Scott W
Mori, Trevor A
Fetal Growth Trajectories and Measures of Insulin Resistance in Young Adults
title Fetal Growth Trajectories and Measures of Insulin Resistance in Young Adults
title_full Fetal Growth Trajectories and Measures of Insulin Resistance in Young Adults
title_fullStr Fetal Growth Trajectories and Measures of Insulin Resistance in Young Adults
title_full_unstemmed Fetal Growth Trajectories and Measures of Insulin Resistance in Young Adults
title_short Fetal Growth Trajectories and Measures of Insulin Resistance in Young Adults
title_sort fetal growth trajectories and measures of insulin resistance in young adults
topic Clinical Research Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10656704/
https://www.ncbi.nlm.nih.gov/pubmed/37246587
http://dx.doi.org/10.1210/clinem/dgad292
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