4.7 Article

Prenatal Exposure to Butylbenzyl Phthalate and Early Eczema in an Urban Cohort

Journal

ENVIRONMENTAL HEALTH PERSPECTIVES
Volume 120, Issue 10, Pages 1475-1480

Publisher

US DEPT HEALTH HUMAN SCIENCES PUBLIC HEALTH SCIENCE
DOI: 10.1289/ehp.1104544

Keywords

butylbenzyl phthalate; eczema; plasticizers

Funding

  1. National Institute of Environmental Health Sciences [R01 ES014393, R01 ES013163, P01 ES09600, R01 ES008977, P30 ES009089]
  2. U.S. Environmental Protection Agency (EPA) [R827027, RD832141, RD834509]
  3. EPA STAR graduate fellowship [FP-91712001]
  4. John and Wendy Neu Family Foundation
  5. Blanchette Hooker Rockefeller Fund
  6. New York Community Trust
  7. Educational Foundation of America
  8. Millstream Fund

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BACKGROUND: Recent cross-sectional studies suggest a link between butylbenzyl phthalate (BBzP) in house dust and childhood eczema. OBJECTIVES: We aimed to evaluate whether concentrations of monobenzyl phthalate (MBzP), the main BBzP metabolite in urine, during pregnancy are associated prospectively with eczema in young children, and whether this association varies by the child's sensitization to indoor allergens or serological evidence of any allergies. METHoDs: MBzP was measured in spot urine samples during the third trimester of pregnancy from 407 African-American and Dominican women residing in New York City in 1999-2006. Repeated questionnaires asked mothers whether their doctor ever said their child had eczema. Child blood samples at 24, 36, and 60 months of age were analyzed for total, anti-cockroach, dust mite, and mouse IgE. Relative risks (RR) were estimated with multivariable modified Poisson regression. Analyses included a multinomial logistic regression model for early- and late-onset eczema versus no eczema through 60 months of age. RESULTS: MBzP was detected in > 99% of samples (geometric mean = 13.6; interquartile range: 5.7-31.1 ng/mL). By 24 months, 30% of children developed eczema, with the proportion higher among African Americans (48%) than among Dominicans (21%) (p < 0.001). An interquartile range increase in log MBzP concentration was associated positively with early-onset eczema (RR = 1.52 for eczema by 24 months; 95% confidence interval: 1.21, 1.91, p = 0.0003, n = 113 reporting eczema/376 total sample), adjusting for urine specific gravity, sex, and race/ethnicity. MBzP was not associated with allergic sensitization, nor did seroatopy modify consistently the MBzP and eczema association. CONCLUSIONS: Prenatal exposure to BBzP may influence the risk of developing eczema in early childhood.

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