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Maternal exposure to PM2.5during pregnancy and asthma risk in early childhood: Consideration of phases of fetal lung development

  • Marnie F. Hazlehurst
  • , Kecia N. Carroll
  • , Christine T. Loftus
  • , Adam A. Szpiro
  • , Paul E. Moore
  • , Joel D. Kaufman
  • , Kipruto Kirwa
  • , Kaja Z. Lewinn
  • , Nicole R. Bush
  • , Sheela Sathyanarayana
  • , Frances A. Tylavsky
  • , Emily S. Barrett
  • , Ruby H.N. Nguyen
  • , Catherine J. Karr

Research output: Contribution to journalArticlepeer-review

Abstract

Background: Increasingly studies suggest prenatal exposure to air pollution may increase risk of childhood asthma. Few studies have investigated exposure during specific fetal pulmonary developmental windows. Objective: To assess associations between prenatal fine particulate matter exposure and asthma at age 4. Methods: This study included mother-child dyads from two pregnancy cohorts - CANDLE and TIDES - within the ECHO-PATHWAYS consortium (births in 2007-2013). Three child asthma outcomes were parent-reported: ever asthma, current asthma, and current wheeze. Fine particulate matter (PM2.5) exposures during the pseudoglandular (5-16 weeks gestation), canalicular (16-24 weeks gestation), saccular (24-36 weeks gestation), and alveolar (36+ weeks gestation) phases of fetal lung development were estimated using a national spatiotemporal model. We estimated associations with Poisson regression with robust standard errors, and adjusted for child, maternal, and neighborhood factors. Results: Children (n = 1,469) were on average 4.3 (SD 0.5) years old, 49% were male, and 11.7% had ever asthma; 46% of women identified as black and 53% had at least a college/technical school degree. A 2 μg/m3 higher PM2.5 exposure during the saccular phase was associated with 1.29 times higher risk of ever asthma [95% confidence interval (CI): 1.06, 1.58]. A similar association was observed with current asthma (risk ratio 1.27, 95% CI: 1.04, 1.54), but not current wheeze (risk ratio 1.11, 95% CI: 0.92, 1.33). Effect estimates for associations during other developmental windows had CIs that included the null. Conclusions: Later phases of prenatal lung development may be particularly sensitive to the developmental toxicity of PM2.5.

Original languageEnglish (US)
Pages (from-to)E130
JournalEnvironmental Epidemiology
Volume5
Issue number2
DOIs
StatePublished - Apr 2 2021

Bibliographical note

Publisher Copyright:
Copyright © 2021 The Authors.

UN SDGs

This output contributes to the following UN Sustainable Development Goals (SDGs)

  1. SDG 3 - Good Health and Well-being
    SDG 3 Good Health and Well-being

Keywords

  • Air pollution
  • Child asthma
  • Developmental Origins of Health and Disease
  • PM
  • Particulate matter
  • prenatal

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