Publication

Associations of Prenatal Exposure to Organophosphate Pesticide Metabolites with Gestational Age and Birth Weight

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Last modified
  • 08/15/2025
Type of Material
Authors
    Stephen A. Rauch, BC Childrens HospitalJoe M. Braun, Harvard UniversityDana Barr, Emory UniversityAntonia M. Calafat, Centers for Disease Control and PreventionJane Khoury, Cincinnati Children’s Hospital Medical CenterM. Angela Montesano, Centers for Disease Control and PreventionKimberly Yolton, Cincinnati Children’s Hospital Medical CenterBruce P. Lanphear, BC Childrens Hospital
Language
  • English
Date
  • 2012-07-01
Publisher
  • National Institute of Environmental Health Sciences (NIEHS)
Publication Version
Copyright Statement
  • EHP is an open-access journal published with support from the National Institute of Environmental Health Sciences, National Institutes of Health. All content is public domain unless otherwise noted.
Final Published Version (URL)
Title of Journal or Parent Work
ISSN
  • 0091-6765
Volume
  • 120
Issue
  • 7
Start Page
  • 1055
End Page
  • 1060
Grant/Funding Information
  • This work was partially supported by grants from the National Institute of Environmental Health Sciences (R01 ES015517, P01 ES11261, T32 ES007069).
Supplemental Material (URL)
Abstract
  • Background: Prenatal exposure to organophosphate (OP) insecticides, a widely used class of pesticides, may be associated with decreased gestational age and lower birth weight. Single nucleotide polymorphisms in paroxanase (PON1) enzyme genotypes may modify the relationships between OP exposure and perinatal outcomes. Objective: We examined the relationship of prenatal OP insecticide exposure, measured using urinary dialkyl phosphate (DAP) metabolite concentrat ions, with gestational age and birth weight. Methods: We measured the concentrations of six nonspecific DAP metabolites of OP insecticides in two maternal spot urine samples collected in a prospective birth cohort. We performed multivariable regression to examine associations between the sum of six DAP concentrations (ΣDAP) with gestational age and birth weight. We also examined whether these associations differed according to infant PON1 192 and PON1-108 genotypes. Results: Among 306 mother-infant dyads, a 10-fold increase in ΣDAP concentrations was associated with a decrease in covariate-adjusted gestational age [-0.5 weeks; 95% confidence interval (CI): -0.8, -0.1] and birth weight (-151 g; CI: -287, -16); the decrements in birth weight were attenuated after adjusting for gestational age. The relationship between ΣDAP concentrations and gestational age was stronger for white (-0.7 weeks; CI: -1.1, -0.3) than for black (-0.1 weeks; 95% CI: -0.9, 0.6) newborns. In contrast, there was a greater decrease in birth weight with increasing urinary ΣDAP concentrations for black (-188 g; CI: -395, 19) than for white (-118 g; CI: -296, 60) newborns. Decrements in birth weight and gestational age associated with ΣDAP concentrations were greatest among infants with PON1192QR and PON-108CT genotypes. Conclusions: Prenatal urinary ΣDAP concentrations were associated with shortened gestation and reduced birth weight in this cohort, but the effects differed by race/ethnicity and PON1192/108 genotypes.
Author Notes
  • Address correspondence to B.P. Lanphear, 3415 Ash St., Vancouver, BC V5Z3E5 Canada. Telephone: (778) 387-3939. Email: blanphear@sfu.ca
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