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Breath Collection from Children for Disease Biomarker Discovery
Published on: February 14, 2019
Urinary Volatile Organic Compound Metabolites Are Associated with Reduced Lung Function in U.S. Children and
Angelico Mendy1, Sara Burcham1, Ashley L Merianos2
1Division of Epidemiology, Department of Environmental and Public Health Sciences, University of Cincinnati College of Medicine, Cincinnati, OH 45229, USA.
Insights
Exposure to common indoor pollutants like acrylamide, styrene, and propylene oxide may negatively impact children's lung function. This study reveals novel associations between specific volatile organic compound (VOC) metabolites and reduced lung capacity in young individuals.
Area of Science:
- Environmental Health
- Pediatric Pulmonology
- Toxicology
Background:
- Volatile organic compounds (VOCs) are prevalent indoor air pollutants.
- Inhalation is a primary exposure route for VOCs.
- The impact of many VOCs on pediatric lung function remains understudied.
Purpose of the Study:
- To investigate the association between urinary VOC metabolites and lung function in children and adolescents.
- To identify specific VOCs that may negatively affect respiratory health in pediatric populations.
Main Methods:
- Analysis of 505 participants aged 6-17 years from the 2011-2012 National Health and Nutrition Examination Survey.
- Utilized multiple linear regression models to assess relationships between VOC metabolites and spirometry outcomes.
- Adjusted for relevant covariates in statistical analyses.
Main Results:
- Urinary metabolites of acrylamide, styrene, propylene oxide, 1-bromopropane, and crotonaldehyde were detected in a majority of participants.
- Higher levels of acrylamide and styrene metabolites were associated with lower forced expiratory volume in 1 second (FEV1) % predicted.
- Elevated propylene oxide metabolites correlated with a reduced FEV1/forced vital capacity (FVC) ratio.
- Significant interactions were observed for crotonaldehyde (in overweight/obese children) and 1-bromopropane (in children with higher cotinine levels) with lung function parameters.
Conclusions:
- Novel associations were identified between specific VOC metabolites (acrylamide, propylene oxide, styrene, 1-bromopropane, crotonaldehyde) and diminished lung function in children and adolescents.
- Findings highlight potential risks of indoor VOCs to pediatric respiratory health.
- Further research is warranted to elucidate mechanisms and inform public health interventions.
Abstract:
(1) Background: Volatile organic compounds (VOCs) are indoor pollutants absorbed by inhalation. The association of several VOCs with lung function in children and adolescents is unknown. (2) Methods: We analyzed 505 participants, 6-17-year-olds from the 2011-2012 National Health and Nutrition Examination Survey. Multiple linear regression models were fitted to estimate the associations of VOC metabolites with spirometry outcomes adjusting for covariates. (3) Results: Urinary metabolites of xylene, acrylamide, acrolein, 1,3-butadiene, cyanide, toluene, 1-bromopropane, acrylonitrile, propylene oxide, styrene, ethylbenzene, and crotonaldehyde were all detected in ≥64.5% of participants. Forced expiratory volume in 1 s (FEV1) % predicted was lower in participants with higher levels of metabolites of acrylamide (β: -7.95, 95% CI: -13.69, -2.21) and styrene (β: -6.33, 95% CI: -11.60, -1.07), whereas the FEV1 to forced vital capacity (FVC) ratio % was lower in children with higher propylene oxide metabolite levels (β: -2.05, 95% CI: -3.49, -0.61). FEV1 % predicted was lower with higher crotonaldehyde metabolite levels only in overweight/obese participants (β: -15.42, 95% CI: -26.76, -4.08) (Pinteraction < 0.001) and with higher 1-bromopropane metabolite levels only in those with serum cotinine > 1 ng/mL (β: -6.26, 95% CI: -9.69, -2.82) (Pinteraction < 0.001). (4) Conclusions: We found novel associations of metabolites for acrylamide, propylene oxide, styrene, 1-bromopropane and crotonaldehyde with lower lung function in children and adolescents.
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