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Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study
BACKGROUND: The genetics of fetal insulin release and/or action have been suggested to affect fetal growth, adult insulin resistance and adult body composition. The genetic correlation between body composition at birth versus glycaemic regulation and body composition in adulthood have, however, not...
Autores principales: | , , , , , |
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Formato: | Online Artículo Texto |
Lenguaje: | English |
Publicado: |
BioMed Central
2018
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Materias: | |
Acceso en línea: | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278142/ https://www.ncbi.nlm.nih.gov/pubmed/30514227 http://dx.doi.org/10.1186/s12881-018-0718-2 |
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author | Hollensted, Mette Ekstrøm, Claus T. Pedersen, Oluf Eiberg, Hans Hansen, Torben Gjesing, Anette Prior |
author_facet | Hollensted, Mette Ekstrøm, Claus T. Pedersen, Oluf Eiberg, Hans Hansen, Torben Gjesing, Anette Prior |
author_sort | Hollensted, Mette |
collection | PubMed |
description | BACKGROUND: The genetics of fetal insulin release and/or action have been suggested to affect fetal growth, adult insulin resistance and adult body composition. The genetic correlation between body composition at birth versus glycaemic regulation and body composition in adulthood have, however, not been well studied. We therefore aimed to investigate these genetic correlations in a family-based cohort. METHODS: A Danish family cohort of 434 individuals underwent an oral glucose tolerance test with subsequent calculation of surrogate measures of serum insulin response and insulin sensitivity. Measures of fetal growth were retrieved from midwife journals. Heritability and genetic correlations were estimated using a variance component model. RESULTS: A high heritability of 0.80 was found for birth weight, whereas ponderal index had a heritability of 0.46. Adult insulin sensitivity measured as Matsuda index was genetically correlated with both birth weight and ponderal index (ρG = 0.36 (95% CI: 0.03; 0.69) and ρG = 0.52 (95% CI, 0.15; 0.89), respectively). Only birth weight showed a significant genetic correlation with adult weight (ρG = 0.38 (95% CI: 0.09; 0.67)) whereas only ponderal index was genetically inversely correlated with fasting insulin (ρG = - 0.47 (95% CI: - 0.86; - 0.08) and area under the curve for insulin release during the oral glucose tolerance test (ρG = - 0.66 (95% CI: - 1.13; - 0.19)). Individual as well as combined adjustment for 45 selected birth weight, obesity and type 2 diabetes susceptibility gene variants did not affect the correlations. CONCLUSIONS: The genetics of both birth weight and ponderal index appear to be under the same genetic influence as adult insulin resistance. Furthermore, ponderal index and adult insulin release seem to be partly shared, as well as the genetics of birth weight and adult weight. Word count abstract: 281. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-018-0718-2) contains supplementary material, which is available to authorized users. |
format | Online Article Text |
id | pubmed-6278142 |
institution | National Center for Biotechnology Information |
language | English |
publishDate | 2018 |
publisher | BioMed Central |
record_format | MEDLINE/PubMed |
spelling | pubmed-62781422018-12-10 Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study Hollensted, Mette Ekstrøm, Claus T. Pedersen, Oluf Eiberg, Hans Hansen, Torben Gjesing, Anette Prior BMC Med Genet Research Article BACKGROUND: The genetics of fetal insulin release and/or action have been suggested to affect fetal growth, adult insulin resistance and adult body composition. The genetic correlation between body composition at birth versus glycaemic regulation and body composition in adulthood have, however, not been well studied. We therefore aimed to investigate these genetic correlations in a family-based cohort. METHODS: A Danish family cohort of 434 individuals underwent an oral glucose tolerance test with subsequent calculation of surrogate measures of serum insulin response and insulin sensitivity. Measures of fetal growth were retrieved from midwife journals. Heritability and genetic correlations were estimated using a variance component model. RESULTS: A high heritability of 0.80 was found for birth weight, whereas ponderal index had a heritability of 0.46. Adult insulin sensitivity measured as Matsuda index was genetically correlated with both birth weight and ponderal index (ρG = 0.36 (95% CI: 0.03; 0.69) and ρG = 0.52 (95% CI, 0.15; 0.89), respectively). Only birth weight showed a significant genetic correlation with adult weight (ρG = 0.38 (95% CI: 0.09; 0.67)) whereas only ponderal index was genetically inversely correlated with fasting insulin (ρG = - 0.47 (95% CI: - 0.86; - 0.08) and area under the curve for insulin release during the oral glucose tolerance test (ρG = - 0.66 (95% CI: - 1.13; - 0.19)). Individual as well as combined adjustment for 45 selected birth weight, obesity and type 2 diabetes susceptibility gene variants did not affect the correlations. CONCLUSIONS: The genetics of both birth weight and ponderal index appear to be under the same genetic influence as adult insulin resistance. Furthermore, ponderal index and adult insulin release seem to be partly shared, as well as the genetics of birth weight and adult weight. Word count abstract: 281. ELECTRONIC SUPPLEMENTARY MATERIAL: The online version of this article (10.1186/s12881-018-0718-2) contains supplementary material, which is available to authorized users. BioMed Central 2018-12-04 /pmc/articles/PMC6278142/ /pubmed/30514227 http://dx.doi.org/10.1186/s12881-018-0718-2 Text en © The Author(s). 2018 Open AccessThis article is distributed under the terms of the Creative Commons Attribution 4.0 International License (http://creativecommons.org/licenses/by/4.0/), which permits unrestricted use, distribution, and reproduction in any medium, provided you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons license, and indicate if changes were made. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated. |
spellingShingle | Research Article Hollensted, Mette Ekstrøm, Claus T. Pedersen, Oluf Eiberg, Hans Hansen, Torben Gjesing, Anette Prior Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study |
title | Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study |
title_full | Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study |
title_fullStr | Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study |
title_full_unstemmed | Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study |
title_short | Genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study |
title_sort | genetic insights into fetal growth and measures of glycaemic regulation and adiposity in adulthood: a family-based study |
topic | Research Article |
url | https://www.ncbi.nlm.nih.gov/pmc/articles/PMC6278142/ https://www.ncbi.nlm.nih.gov/pubmed/30514227 http://dx.doi.org/10.1186/s12881-018-0718-2 |
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