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Increased Impact of Air Pollution on Lung Function in Preterm versus Term Infants: The BILD Study
Fabienne Decrue1,2, Olga Gorlanova1,2, Yasmin Salem1,2
1University Children's Hospital Basel UKBB.
Insights
Preterm infants are more vulnerable to prenatal air pollution, experiencing greater lung function impairment. Exposure to particulate matter (PM10) during pregnancy negatively impacts lung development in these infants.
Area of Science:
- Environmental Health
- Neonatology
- Pediatric Pulmonology
Background:
- Infants born prematurely possess a diminished capacity to manage oxidative stress post-birth.
- Prenatal exposure to air pollution may disproportionately affect lung development in preterm infants compared to term infants.
Purpose of the Study:
- To investigate the association between exposure to particulate matter (PM10) and nitrogen dioxide with lung function in preterm and term infants.
- To explore the impact of prenatal air pollution on markers of inflammation and oxidative stress, specifically fractional exhaled nitric oxide (FeNO).
Main Methods:
- Prospective BILD birth cohort study involving 254 preterm and 517 term infants.
- Analysis of associations between PM10 and nitrogen dioxide exposure during pregnancy and infant lung function at 44 weeks' postconceptional age.
- Use of multilevel mixed-effects models adjusted for confounders, including analysis of FeNO levels.
Main Results:
- Significant associations were found between PM10 exposure during the second trimester of pregnancy and altered lung function and FeNO levels in both preterm and term infants.
- Preterm infants exhibited stronger positive associations between PM10 exposure and lung function impairment compared to term infants (p-interaction=0.04).
- Differences in PM10 and FeNO associations were observed between moderate-to-late preterm and term infants, with a significant interaction effect (p-interaction=0.006).
Conclusions:
- Preterm infants demonstrate heightened susceptibility to prenatal air pollution, leading to more significant postnatal lung function deficits.
- Fractional exhaled nitric oxide (FeNO) levels highlight distinct inflammatory and oxidative stress responses in preterm infants compared to term infants following air pollution exposure.
Abstract:
Rationale: Infants born prematurely have impaired capacity to deal with oxidative stress shortly after birth. Objectives: We hypothesize that the relative impact of exposure to air pollution on lung function is higher in preterm than in term infants. Methods: In the prospective BILD (Basel-Bern Infant Lung Development) birth cohort of 254 preterm and 517 term infants, we investigated associations of particulate matter ⩽10 μm in aerodynamic diameter (PM10) and nitrogen dioxide with lung function at 44 weeks' postconceptional age and exhaled markers of inflammation and oxidative stress response (fractional exhaled nitric oxide [FeNO]) in an explorative hypothesis-driven study design. Multilevel mixed-effects models were used and adjusted for known confounders. Measurements and Main Results: Significant associations of PM10 during the second trimester of pregnancy with lung function and FeNO were found in term and preterm infants. Importantly, we observed stronger positive associations in preterm infants (born 32-36 wk), with an increase of 184.9 (95% confidence interval [CI], 79.1-290.7) ml/min [Formula: see text]e per 10-μg/m3 increase in PM10, than in term infants (75.3; 95% CI, 19.7-130.8 ml/min) (pprematurity × PM10 interaction = 0.04, after multiple comparison adjustment padj = 0.09). Associations of PM10 and FeNO differed between moderate to late preterm (3.4; 95% CI, -0.1 to 6.8 ppb) and term (-0.3; 95% CI, -1.5 to 0.9 ppb) infants, and the interaction with prematurity was significant (pprematurity × PM10 interaction = 0.006, padj = 0.036). Conclusions: Preterm infants showed significantly higher susceptibility even to low to moderate prenatal air pollution exposure than term infants, leading to increased impairment of postnatal lung function. FeNO results further elucidate differences in inflammatory/oxidative stress response when comparing preterm infants with term infants.
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