Prenatal phthalate exposure, oxidative stress-related genetic vulnerability and early life neurodevelopment: A birth cohort study

Neurotoxicology. 2020 Sep:80:20-28. doi: 10.1016/j.neuro.2020.05.006. Epub 2020 May 30.

Abstract

Prenatal phthalate chemicals may have adverse effects on brain development by various mechanisms including oxidant damage. However, birth cohort findings have been conflicting. This study aimed to (i) investigate the interplay between maternal prenatal phthalate levels, infant genetic vulnerability to oxidative stress, and child neurodevelopment and (ii) examine combined putative oxidant exposures. In a population-based birth cohort of 1064 women with prenatal recruitment in Victoria, Australia, maternal urine was collected at 36 weeks of pregnancy and phthalate metabolite concentrations measured. An unweighted genetic score for oxidative stress was made using a candidate gene approach. Cognition was assessed using the BAYLEY-III at two years (n = 678). Parents completed questionnaires for doctor diagnosed autism spectrum disorder (ASD) (1.4 %), ASD traits (4.9 %) and child inattention/hyperactivity (n = 791). Analyses included multiple linear and logistic regression. Higher prenatal phthalate levels and a higher oxidative stress genetic score were each associated with subsequent ASD. Several oxidative stress-related SNPs modified the association between prenatal phthalates and ASD and other outcomes. Consistent patterns were evident across gene score-phthalate combinations for cognition, ASD, ASD traits and inattention/hyperactivity. Other putative oxidant factors such as prenatal smoking further increased risk. Prenatal phthalate levels and infant oxidative stress-related genetic vulnerability are associated with adverse neurodevelopment. Combined exposures are important. Current recommendations and regulation on maternal phthalate exposure during pregnancy require re-evaluation.

Keywords: Autism spectrum disorder; Cognition; Genetic score; Oxidative stress; Phthalates; Pregnancy.

Publication types

  • Research Support, Non-U.S. Gov't
  • Twin Study

MeSH terms

  • Age Factors
  • Autism Spectrum Disorder / chemically induced*
  • Autism Spectrum Disorder / diagnosis
  • Autism Spectrum Disorder / genetics*
  • Autism Spectrum Disorder / physiopathology
  • Child Behavior / drug effects*
  • Child Development / drug effects*
  • Child, Preschool
  • Cognition / drug effects
  • Environmental Pollutants / adverse effects*
  • Female
  • Gene Expression Regulation, Developmental
  • Gene-Environment Interaction
  • Gestational Age
  • Humans
  • Maternal Exposure / adverse effects
  • Nervous System / drug effects*
  • Nervous System / growth & development
  • Nervous System / metabolism
  • Oxidative Stress / genetics*
  • Phthalic Acids / adverse effects*
  • Polymorphism, Single Nucleotide*
  • Pregnancy
  • Prenatal Exposure Delayed Effects*
  • Risk Assessment
  • Risk Factors
  • Twins

Substances

  • Environmental Pollutants
  • Phthalic Acids
  • phthalic acid