A pilot study for foetal exposure to multiple persistent organic pollutants and the development of infant atopic dermatitis in modern Japanese society

Chemosphere. 2014 Jan:94:48-52. doi: 10.1016/j.chemosphere.2013.09.009. Epub 2013 Sep 27.

Abstract

Increasing evidence supports that harmful chemicals accumulating in the human body may pose a significant threat to infant health through foetal exposure. Persistent organic pollutants (POPs) are thought to enhance the risk for later development of allergic disease like atopic dermatitis (AD). However, few studies have evaluated the effect of foetal exposure to various POPs on the development of AD in early infancy. Here, we describe the impact of foetal exposure to a number of POPs on the occurrence of AD in 7-month-old infants. The participants were 81 infants with or without AD who participated in a birth cohort study, where the concentrations of 15 polychlorinated biphenyl (PCBs) congeners, dichlorodiphenyltrichloroethane (p,p'-DDT), dichlorodiphenyldichloroethylene (p,p'-DDE), β-hexachlorocyclohexane (β-HCH), hexachlorobenzene (HCB), cis-nonachlor, trans-nonachlor, mirex, oxychlordane, and 27 polybrominated diphenyl ether (PBDEs) congeners were measured in the umbilical cord tissues collected immediately after birth. At 7 months, 27 of the 81 infants (33.8%) were diagnosed with AD. Of all POPs examined, total concentrations of 27 PBDE congeners were associated with a significantly decreased incidence of AD. Notably, the concentration of 27 PBDEs was significantly lower in AD infants than in non-AD infants (P<0.01), and the risk of AD development decreased with increasing PBDE levels. These results suggest that foetal exposure to PBDEs is a possible contributing factor to reducing AD in early infancy.

Keywords: Atopic dermatitis; Foetal exposure; Infants; Persistent organic pollutants.

Publication types

  • Research Support, Non-U.S. Gov't

MeSH terms

  • Chlordan / analogs & derivatives
  • Chlordan / metabolism
  • DDT / metabolism
  • Dermatitis, Atopic / chemically induced
  • Dermatitis, Atopic / epidemiology*
  • Dermatitis, Atopic / metabolism
  • Dichlorodiphenyl Dichloroethylene / metabolism
  • Environmental Exposure / analysis*
  • Environmental Exposure / statistics & numerical data
  • Environmental Pollutants / analysis
  • Environmental Pollutants / metabolism*
  • Female
  • Hexachlorobenzene / metabolism
  • Hexachlorocyclohexane / metabolism
  • Humans
  • Hydrocarbons, Chlorinated / metabolism
  • Infant
  • Infant, Newborn
  • Japan
  • Male
  • Maternal Exposure / statistics & numerical data
  • Mirex / metabolism
  • Pilot Projects
  • Polychlorinated Biphenyls / metabolism
  • Young Adult

Substances

  • Environmental Pollutants
  • Hydrocarbons, Chlorinated
  • Chlordan
  • oxychlordane
  • nonachlor
  • Dichlorodiphenyl Dichloroethylene
  • Hexachlorobenzene
  • Hexachlorocyclohexane
  • DDT
  • Polychlorinated Biphenyls
  • beta-hexachlorocyclohexane
  • Mirex