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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.
Affiliation
  • Hollensted M; Section of Metabolic Genetics, The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200, Copenhagen, Denmark. mette.hollensted@sund.ku.dk.
  • Ekstrøm CT; The Danish Diabetes Academy, Odense, Denmark. mette.hollensted@sund.ku.dk.
  • Pedersen O; Section of Biostatistics, Department of Public Health, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Eiberg H; Section of Metabolic Genetics, The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200, Copenhagen, Denmark.
  • Hansen T; Department of Cellular and Molecular Medicine, Faculty of Health and Medical Sciences, University of Copenhagen, Copenhagen, Denmark.
  • Gjesing AP; Section of Metabolic Genetics, The Novo Nordisk Foundation Center for Basic Metabolic Research, Faculty of Health and Medical Sciences, University of Copenhagen, Blegdamsvej 3B, DK-2200, Copenhagen, Denmark.
BMC Med Genet ; 19(1): 207, 2018 12 04.
Article in En | MEDLINE | ID: mdl-30514227
ABSTRACT

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.
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Full text: 1 Database: MEDLINE Main subject: Blood Glucose / Insulin Resistance / Quantitative Trait, Heritable / Fetal Development / Adiposity / Insulin Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Pregnancy Country/Region as subject: Europa Language: En Journal: BMC Med Genet Journal subject: GENETICA MEDICA Year: 2018 Type: Article Affiliation country: Denmark

Full text: 1 Database: MEDLINE Main subject: Blood Glucose / Insulin Resistance / Quantitative Trait, Heritable / Fetal Development / Adiposity / Insulin Type of study: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Limits: Adult / Female / Humans / Male / Pregnancy Country/Region as subject: Europa Language: En Journal: BMC Med Genet Journal subject: GENETICA MEDICA Year: 2018 Type: Article Affiliation country: Denmark