Ambient air pollution during pregnancy and cardiometabolic biomarkers in cord blood
Chloe Friedman1,2, Dana Dabelea1,2,3, Lizan D Bloemsma1,2
1Department of Epidemiology, Colorado School of Public Health, University of Colorado Anschutz Medical Campus, Aurora, Colorado.
Insights
Prenatal exposure to ozone (O3) air pollution was linked to higher cord blood insulin levels in newborns. This suggests metabolic disruption may be detectable at birth, impacting long-term cardiometabolic health.
Area of Science:
- Environmental Health
- Pediatrics
- Metabolic Health
Background:
- Prenatal exposure to ambient air pollution is linked to adverse childhood cardiometabolic outcomes.
- Evidence of metabolic disruption from prenatal air pollution exposure at birth is not well understood.
- The Healthy Start study examined mother-infant pairs to investigate this association.
Purpose of the Study:
- To investigate the association between prenatal exposure to ambient air pollution and cord blood cardiometabolic biomarkers.
- To determine if metabolic disruption from air pollution is identifiable at birth.
Main Methods:
- Estimated daily concentrations of fine particulate matter (PM2.5) and ozone (O3) using inverse-distance-weighted interpolation.
- Averaged air pollution estimates by trimester, full pregnancy, and the 7 and 30 days prior to delivery.
- Used multivariable linear regression to assess associations between air pollution and cord blood biomarkers (glucose, insulin, GIR, leptin, HDL, non-HDL, free fatty acids, triglycerides).
Main Results:
- Higher ozone (O3) concentrations during pregnancy were consistently associated with higher cord blood insulin and lower glucose/insulin ratio (GIR).
- An interquartile range increase in full pregnancy O3 was associated with higher cord blood insulin.
- Particulate matter (PM2.5) showed positive but generally nonsignificant associations with leptin and lipids.
Conclusions:
- Prenatal ozone (O3) exposure is positively associated with cord blood insulin levels.
- Metabolic disruption may be identifiable at birth following prenatal air pollution exposure.
- Further research is needed to understand the long-term health implications for offspring.
Abstract:
Prenatal air pollution exposure has been associated with adverse childhood cardiometabolic outcomes. It is unknown whether evidence of metabolic disruption associated with air pollution is identifiable at birth. We examined exposure to prenatal ambient air pollution and cord blood cardiometabolic biomarkers among 812 mother-infant pairs in the Healthy Start study.
Methods:
Using inverse-distance-weighted interpolation of ambient concentrations obtained from stationary monitors, we estimated daily particulate matter ≤2.5 micrometers (PM2.5) and ozone (O3) concentrations at participant residences. Daily estimates were averaged by trimester, full-pregnancy, and the 7 and 30 days prior to delivery. Associations of air pollution with the following cord blood biomarkers were estimated via multivariable linear regression: glucose, insulin, glucose/insulin ratio (GIR), leptin, high-density lipoprotein (HDL) cholesterol, non-HDL cholesterol, free fatty acids, and triglycerides.
Results:
In this Denver-based cohort, PM2.5 concentrations were lower than in many US urban areas, but O3 concentrations regularly exceeded federal air quality standards. Higher O3 concentrations during pregnancy were consistently associated with higher insulin and lower GIR in cord blood. For example, an interquartile range increase in full pregnancy O3 (6.3 parts per billion [ppb]) was associated with 0.13 log-µIU/ml (95% confidence interval [CI] = 0.04, 0.22) higher cord blood insulin, after adjusting for PM2.5 and other confounders. We found positive, but generally nonsignificant, associations between PM2.5 and leptin and isolated associations between pollutants during certain exposure periods and lipids.
Conclusions:
In this cohort with moderately high O3 exposure, prenatal concentrations of O3 were positively associated with cord blood insulin. Future studies should examine the implications for offspring long-term health.
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