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Updated: Jun 8, 2026

Breath Collection from Children for Disease Biomarker Discovery
Published on: February 14, 2019
Exhaled NO among inner-city children in New York City
Matthew S Perzanowski1, Adnan Divjan, Robert B Mellins
1Department of Environmental Health Sciences, Mailman School of Public Health, Columbia University, New York, NY 10032, USA. mp2217@columbia.edu
Insights
Fractional exhaled nitric oxide (FeNO) indicates airway inflammation in children with asthma symptoms. Early environmental tobacco smoke (ETS) exposure correlates with higher FeNO, while later exposure shows an inverse relationship, suggesting complex interactions.
Area of Science:
- Pediatric Pulmonology
- Environmental Health
- Biomarker Research
Background:
- Fractional exhaled nitric oxide (FeNO) is a proposed biomarker for airway inflammation in asthma research.
- Inner-city children face unique environmental exposures impacting respiratory health.
Purpose of the Study:
- To evaluate the link between FeNO and asthma symptoms in 7-year-old inner-city children.
- To investigate the association of past and current environmental tobacco smoke (ETS) exposure with FeNO levels.
Main Methods:
- Longitudinal asthma study involving FeNO and lung function tests at age 7.
- Assessment of seroatopy via allergen-specific immunoglobulin E (IgE) levels.
- Questionnaire-based evaluation of ETS exposure at ages 4 and 7.
Main Results:
- Children reporting wheeze had significantly higher FeNO levels (17.0 vs. 11.0 ppb).
- FeNO remained associated with wheeze after adjusting for seroatopy and FEV1.
- FeNO at age 7 positively correlated with ETS exposure at age 4 but inversely with ETS at age 7.
Conclusions:
- FeNO is a relevant outcome measure for asthma studies in inner-city populations, showing association with current wheeze.
- The positive association between early ETS exposure and airway inflammation warrants further investigation in larger cohorts.
Background:
Fractional exhaled nitric oxide (FeNO) has been proposed as a biomarker of airway inflammation for cohort studies of asthma.
Objectives:
To assess the association between FeNO and asthma symptoms among 7-year-old children living in an inner-city community. To test the association between environmental tobacco smoke (ETS) exposure (previous and current) and FeNO among these children.
Methods:
As part of a longitudinal study of asthma, children recruited in Head Start centers at age 4 had offline FeNO and lung function testing at age 7. Children with allergen-specific immunoglobulin E (IgE) (≥0.35 IU/mL) at age 7 were considered seroatopic. ETS exposure at ages 4 and 7 was assessed by questionnaire.
Results:
Of 144 participating children, 89 had complete questionnaire data and achieved valid FeNO and lung function tests. Children with reported wheeze in the previous 12 months (n = 19) had higher FeNO than those without wheeze (n = 70) (geometric means 17.0 vs. 11.0 ppb, p = .005). FeNO remained significantly associated with wheeze (p = .031), after adjusting for seroatopy and forced expiratory volume in 1 second (FEV₁) in multivariable regression. FeNO at age 7 was positively associated with domestic ETS exposure at age 4 (29%) (β = 0.36, p = .015) but inversely associated with ETS exposure at age 7 (16%) (β = -0.74, p < .001).
Conclusions:
Given its association with current wheeze, independent of seroatopy and lung function, FeNO provides a relevant outcome measure for studies in inner-city communities. While compelling, the positive association between ETS exposure at age 4 and a marker of airway inflammation at age 7 should be confirmed in a larger study.
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