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Updated: Jun 16, 2026

Modifying Levels of Maternal Dietary Folic Acid or Choline to Study the Impact of Deficiencies on Offspring Health Outcomes
Published on: June 28, 2024
Per- and polyfluoroalkyl substances, vitamin D, and risk of preterm birth in a Canadian cohort
Mandy Fisher1, James Owen1, Leonora Marro1
1Environmental Health Science and Research Bureau, Health Canada, Ottawa, Ontario, Canada.
Background:
Vitamin D, which is essential for calcium and phosphorus homeostasis, may also influence immune regulation and offer protection against preterm birth (PTB). Per- and polyfluoroalkyl substances (PFAS) are associated with both increases and decreases in 25-hydroxyvitamin D (25OHD) concentrations and have been shown to compete for binding sites on the vitamin D receptor (VDR). We investigated associations between PFAS and preterm birth, and the potential modification by vitamin D status and single nucleotide polymorphisms (SNPs) of the VDR.
Methods:
We used adjusted discrete-time survival models for individual PFAS, and quantile g-computation for the PFAS mixture. Effect modification was investigated (additive and multiplicative) by first-trimester vitamin D status (≥vs. < 50 nmol/L 25OHD) and four VDR variants: ApaI (rs7975232), BsmI (rs1544410), TaqI (rs731236) and FokI (rs2228570).
Results:
Among 1857 singleton births, 114 (6%) were PTBs. Each doubling of perfluorononanoic acid (PFNA) was associated with an approximate 30% increase in the odds of PTB. We found significant qualitative interactions between a number of PFAS and vitamin D status, with elevated risk specific to those with sufficent vitamin D status (≥50 nmol/L) for PFNA (OR = 1.56, 95% CI:1.15, 2.12). We observed effect modification of the association between PFNA and PFDA by some VDR genotypes. The stratified analysis showed elevated odds among genotypes of ApaI (Aa, OR = 1.78, 95% CI: 1.19, 2.60), BsmI (BB, OR = 1.75, 95% CI: 1.13, 2.64), and TaqI (TT, OR = 1.73, 95% CI: 1.13, 2.59) with each doubling in PFNA. Perfluorodecanoic acid (PFDA) was associated with an increased odds of PTB among those homozygous for the major alleles of BsmI (OR BB = 1.76, 95% CI: 1.17, 2.58) and TaqI (ORTT = 1.65, 95% CI: 1.13, 2.38).
Conclusions:
PFNA exposure was associated with elevated odds of PTB, with evidence of modification by vitamin D status and VDR genotype. PFAS may disrupt receptor-mediated pathways, producing pleiotropic effects. We postulate the observed modification by vitamin D status is partly due to confounding by fish consumption. Further investigation into these associations in other pregnancy cohorts is warranted.
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