Background
Significance of exhaled nitric oxide (FeNO) levels in children with sickle cell anemia (SCA) is unclear, but increased levels may be associated with features of asthma and thus increased morbidity.
Objectives
To determine factors associated with FeNO and whether FeNO levels are associated with increased rates of acute chest syndrome (ACS) and pain.
Methods
All participants had SCA, were part of the prospective, observational Sleep and Asthma Cohort study, and had the following assessments: FeNO, spirometry, blood samples analyzed for hemoglobin, white blood cell count, eosinophils and total serum IgE, questionnaires about child medical and family history, and review of medical records.
Results
The analytic sample included 131 children with SCA, median age 11.2 years (range 6-18) followed for a mean of 16.2 years, including a mean 5.1 years after the baseline FeNO data measurements. In multivariable analyses higher FeNO was associated with ln(IgE) (p<0.001), and the highest quartile of peripheral eosinophil count (p=0.03), but not wheezing symptoms, baseline spirometry indices, or response to bronchodilator. Multivariable analyses identified that incident rate of ACS was associated with ln(FeNO) (p=0.03) as well as male gender (p=0.025), wheezing causing shortness of breath (p=0.002), and ACS <4 years of age (p <0.001). FeNO was not associated with future pain episodes.
Conclusions
Steady state FeNO was not associated with an asthma diagnosis, wheezing symptoms, lung function measures, or prior sickle cell morbidity, but was associated with markers of atopy and increased risk of future ACS events.