Abstract

BackgroundThe 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.MethodsA 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.ResultsA 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.ConclusionsThe 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.

Highlights

  • Low birth weight associates with adult insulin resistance, hypertension, coronary-artery disease and type 2 diabetes mellitus (T2DM) [1, 2], possibly due to maternal malnutrition [3, 4] or an insulin-resistant/-deficient genotype of the foetus [5]

  • The ~ 100 obesity susceptibility loci identified so far [11] appear to have a limited influence on birth weight [12, 13], despite the identification of genetic correlations between birth weight and traits related to adult obesity, including body mass index (BMI), waist and waist-hip ratio using linkage disequilibrium (LD) score regression [14]

  • We aimed to examine whether single nucleotide polymorphisms (SNPs) known to associate with birth weight, adult risk of obesity or adult risk of T2DM may explain any shared genetics between the investigated traits

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Summary

Introduction

Low birth weight associates with adult insulin resistance, hypertension, coronary-artery disease and type 2 diabetes mellitus (T2DM) [1, 2], possibly due to maternal malnutrition [3, 4] or an insulin-resistant/-deficient genotype of the foetus [5] The latter hypothesis, known as the fetal insulin hypothesis, suggests that genetically induced insulin resistance or altered insulin secretion causes impaired insulin-mediated growth in the foetus and insulin resistance/insulin deficiency in adult life [5]. LD score regression is, based on summary statistics from previous GWAS, and the effect of rare genetic variation is not considered Neither do these large-scale studies include detailed phenotypes related to adult glycaemic regulation and body composition. We aimed to investigate these genetic correlations in a family-based cohort

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