Environmental and genetic determinants of vitamin D insufficiency in 12-month-old infants

J Steroid Biochem Mol Biol. 2014 Oct:144 Pt B:445-54. doi: 10.1016/j.jsbmb.2014.08.018. Epub 2014 Aug 29.

Abstract

We aimed to investigate the relationship between genetic and environmental exposure and vitamin D status at age one, stratified by ethnicity. This study included 563 12-month-old infants in the HealthNuts population-based study. DNA from participants' blood samples was genotyped using Sequenom MassARRAY MALDI-TOF system on 28 single nucleotide polymorphisms (SNPs) in six genes. Using logistic regression, we examined associations between environmental exposure and SNPs in vitamin D pathway and filaggrin genes and vitamin D insufficiency (VDI). VDI, defined as serum 25-hydroxyvitamin D3(25(OH)D3) level ≤50nmol/L, was measured using liquid chromatography-tandem mass spectrometry (LC-MS/MS). Infants were stratified by ethnicity determined by parent's country of birth. Infants formula fed at 12 months were associated with reduced odds of VDI compared to infants with no current formula use at 12 months. This association differed by ethnicity (Pinteraction=0.01). The odds ratio (OR) of VDI was 0.29 for Caucasian infants (95% CI, 0.18-0.47) and 0.04 for Asian infants (95% CI, 0.006-0.23). Maternal vitamin D supplementation during pregnancy and/or breastfeeding were associated with increased odds of infants being VDI (OR, 2.39; 95% CI, 1.11-5.18 and OR, 2.5; 95% CI, 1.20-5.24 respectively). Presence of a minor allele for any GC SNP (rs17467825, rs1155563, rs2282679, rs3755967, rs4588, rs7041) was associated with increased odds of VDI. Caucasian infants homozygous (AA) for rs4588 had an OR of 2.49 of being associated with VDI (95% CI, 1.19-5.18). In a country without routine infant vitamin D supplementation or food chain fortification, formula use is strongly associated with a reduced risk of VDI regardless of ethnicity. There was borderline significance for an association between filaggrin mutations and VDI. However, polymorphisms in vitamin D pathway related genes were associated with increased likelihood of being VDI in infancy.

Keywords: Breastfeeding; Cohort studies; Genetic association studies; Infant formula; SNPs; Vitamin D.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase / genetics
  • Asian People / genetics
  • Breast Feeding
  • Cholestanetriol 26-Monooxygenase / genetics
  • Cytochrome P450 Family 2
  • Diet
  • Dietary Supplements
  • Environment
  • Environmental Exposure
  • Female
  • Filaggrin Proteins
  • Humans
  • Infant
  • Infant Formula
  • Intermediate Filament Proteins / genetics
  • Odds Ratio
  • Polymorphism, Single Nucleotide
  • Pregnancy
  • Receptors, Calcitriol / genetics
  • Seasons
  • Ultraviolet Rays
  • Victoria / epidemiology
  • Vitamin D / administration & dosage
  • Vitamin D Deficiency / epidemiology*
  • Vitamin D Deficiency / etiology*
  • Vitamin D-Binding Protein / genetics
  • Vitamin D3 24-Hydroxylase / genetics
  • White People / genetics

Substances

  • FLG protein, human
  • Filaggrin Proteins
  • Intermediate Filament Proteins
  • Receptors, Calcitriol
  • Vitamin D-Binding Protein
  • Vitamin D
  • Cytochrome P450 Family 2
  • CYP2R1 protein, human
  • Cholestanetriol 26-Monooxygenase
  • CYP24A1 protein, human
  • Vitamin D3 24-Hydroxylase
  • 25-Hydroxyvitamin D3 1-alpha-Hydroxylase