RATIONALE
Neighborhood disadvantage (ND) has been associated with sleep-disordered breathing (SDB) in children. However, the association between ND and SDB symptom burden and quality of life (QOL) has not yet been studied.
OBJECTIVE
To evaluate associations between ND with SDB symptom burden and QOL.
METHODS
Cross-sectional analyses were performed on 453 children, ages 3-12.9 years, with mild SDB (habitual snoring and apnea-hypopnea index <3/hour) enrolled in the Pediatric Adenotonsillectomy Trial for Snoring (PATS) multicenter study. The primary exposure, neighborhood disadvantage, was characterized by the Child Opportunity Index (COI), range 0-100, in which lower values (specifically COI ≤40) signify less advantageous neighborhoods. The primary outcomes were QOL assessed by the OSA-18 questionnaire (range 18-126) and SDB symptom burden assessed by the Pediatric Sleep Questionnaire - Sleep-Related Breathing Disorder (PSQ-SRBD) scale (range 0-1). The primary model was adjusted for age, sex, race, ethnicity, maternal education, recruitment site, and season. Additionally, we explored the role of BMI percentile, environmental tobacco smoke (ETS), and asthma in these associations.
RESULTS
The sample included 453 children (16% Hispanic, 26% Black or African American, 52% White or Caucasian, and 6% Other). COI mean (SD) was 50.3 (29.4), and 37% (n=169) of participants lived in disadvantaged neighborhoods. Poor SDB-related QOL (OSA-18 ≥60) and high symptom burden (PSQ-SRBD ≥0.33) were found in 30% (n=134) and 75% (n=341) of participants, respectively. In adjusted models, a COI increase by 1 SD (i.e., more advantageous neighborhood) was associated with an improvement in OSA-18 score by 2.5 points (95% CI: -4.34, -0.62) and in PSQ-SRBD score by 0.03 points (95% CI: -0.05, -0.01). These associations persisted after adjusting for BMI percentile, ETS, or asthma. Associations between COI and SDB-related QOL attenuated by 23% and 10% after adjusting for ETS or asthma, respectively.
CONCLUSIONS
Neighborhood disadvantage was associated with poorer SDB-related QOL and greater SDB symptoms. Associations were partially attenuated after considering the effects of ETS or asthma. The findings support efforts to reduce ETS and neighborhood-level asthma-related risk factors and identify other neighborhood-level factors that contribute to SDB symptom burden as strategies to address sleep-health disparities.