Prenatal heavy metal exposures and atopic dermatitis with gender difference in 6-month-old infants using

Seulbi Lee1, Sung Kyun Park2, Hyesook Park3

  • 1Occupational and Environmental Medicine, College of Medicine, Ewha Womans University, Seoul, Republic of Korea; Department of Epidemiology, School of Public Health, University of Michigan, Ann arbor, MI, United States.

Environmental Research
|February 18, 2021
PubMed

Insights

Prenatal lead exposure may increase infant atopic dermatitis (AD) risk, particularly in boys. This study highlights potential gender differences in heavy metal-induced AD development during critical pregnancy periods.

Area of Science:

  • Environmental Health
  • Pediatric Allergy
  • Toxicology

Background:

  • Prenatal exposure to heavy metals is linked to allergic conditions.
  • Limited research exists on gender-specific associations between prenatal heavy metal exposure and infant atopic dermatitis (AD).

Purpose of the Study:

  • To investigate the gender-specific relationship between prenatal exposure to multiple heavy metals (lead, mercury, cadmium) and the incidence of AD in 6-month-old infants.
  • Utilize data from the prospective Mothers and Children's Environmental Health (MOCEH) study.

Main Methods:

  • Analysis of 738 mother-child pairs from the MOCEH cohort.
  • Measurement of lead, mercury, and cadmium levels in maternal blood during early and late pregnancy.
  • Application of multivariate regression and group Lasso models to assess multi-pollutant effects and interactions, considering nonlinear associations.

Main Results:

  • A total of 200 infant AD cases were identified.
  • Increased lead exposure in late pregnancy was associated with higher AD risk in boys (ORs up to 2.40).
  • A weaker association was observed for lead exposure in girls.

Conclusions:

  • Prenatal lead exposure, especially in late pregnancy, may elevate the risk of AD in infants, with a notable gender difference observed.
  • Further research is warranted to confirm specific susceptibility windows and the mechanisms behind gender differences in lead-induced AD.
Abstract