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Journal Article Ppublish 2 citations

PubMed: 39171784 DOI: 10.1002/ppul.27222

PM2.5 exposure and household income are associated with lung function abnormalities in children with sickle cell disease.

Pediatr Pulmonol 59(12):3419-3425

Authors: Jelte Kelchtermans, Julian Allen, Anita Bhandari

Affiliations

  • Division of Pulmonary and Sleep Medicine, Children's Hospital of Philadelphia, Philadelphia, Pennsylvania, USA.
  • Department of Pediatrics, Perelman School of Medicine, University of Pennsylvania, Philadelphia, Pennsylvania, USA.

Abstract

RATIONALE

Cardiopulmonary dysfunction is a major contributor to mortality among persons with sickle cell disease (pwSCD). Despite this, little is known regarding environmental drivers of lung function decline.

OBJECTIVE

We hypothesized that environmental and socioeconomic variables have a significant effect on lung function in pwSCD that can be detected by spirometry.

METHODS

We retrospectively analyzed all spirometry results from pwSCD followed in the Pediatric Pulmonology clinic at the Children's Hospital of Philadelphia since 1 January 2016.

RESULTS

The study included 349 spirometry tests from 128 patients, primarily "Black or African American" (88%) and male (61%). More frequent exposure to PM2.5 above 25 μg/m was associated with higher odds of obstruction. Specifically, when compared to incidence of exposure to PM2.5 above 25 μg/m <25th percentile, both pwSCD exposed to 25th-75th percentile and pwSCD >75th percentile had higher odds of obstruction on spirometry (25th-75th: odds ratio [OR]: 9.6, p = .017; >75th: OR: 31.85, p = .002) despite correction for potential confounders. Similarly, median household income below the mean was associated with higher odds of restriction (OR: 4.37; p = .009).

CONCLUSIONS

We report higher odds of obstruction in pwSCD frequently exposed to PM2.5 concentrations above 25 μg/m and higher odds of restriction in pwSCD with lower household income. Our findings link spirometry patterns to modifiable risk factors indicating that there may opportunities for early intervention in pwSCD that have been referred to a pulmonology clinic. Further research is needed to assess if these findings can be generalized to the wider population of pwSCD.

MeSH

Cells, Lung, Anemia, Sickle Cell, Respiratory System, Income, Spirometry, Pediatrics, Child

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