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Assessing the health risk of living near composting facilities on lung health, fungal and bacterial disease in cystic fibrosis: a UK CF Registry study

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journal contribution
posted on 2023-07-25, 15:52 authored by Muhammad Saleem Khan, Philippa Douglas, Anna L Hansell, Nicholas J Simmonds, Frederic B Piel

Aim

To explore the health risk of living near permitted composting sites (PCSs) on disease severity in children and adults with cystic fibrosis (CF) across the UK.  METHODS: A semi-individual cross-sectional study was used to examine the risk of disease severity in people with CF (pwCF) within and beyond 4 km of PCSs in the UK in 2016. All pwCF registered in the UK CF Registry were eligible for this study. Linear and Poisson regressions, adjusted for age, gender, genotype, BMI, Pseudomonas aeruginosa and deprivation, were used to quantify associations between distance to a PCS and percent predicted forced expiratory volume in one second (ppFEV1), pulmonary exacerbations (#IVdays), and fungal and bacterial infections.

Results

The mean age of the 9,361 pwCF (3,931 children and 5,430 adults) studied was 20.1 (SD = 14.1) years; 53.3% were male; and 49.2% were homozygous F508del. Over 10% of pwCF (n = 1,015) lived within 4 km of a PCS. We found no statistically significant difference in ppFEV1 and #IVdays/year in children. However, in adults, ppFEV1 was -1.07% lower (95% confidence interval (CI): -2.29%, 0.16%) and #IVdays/year were 1.02 day higher (95%CI: 1.01, 1.04) within 4 km of a PCS. Furthermore, there were statistically significant differences in mean ppFEV1 in CF adults with Aspergillus fumigatus (58.2.% vs 62.0%, p = 0.005) and Candida spp. (56.9% vs 59.9%, p = 0.029) residing within 4 km of a PCS. No associations were identified for allergic bronchopulmonary aspergillosis, P. aeruginosa or Staphylococcus aureus.

Conclusions

This novel national study provides evidence that adults with CF living near a PCS may experience small reductions in lung function, an increased risk of pulmonary exacerbations, and more frequent fungal infections. If confirmed by studies using refined exposure assessment methods accounting for bioaerosol dispersion, these results could have important implications for the living environment of pwCF.

Funding

This study was co-funded by UK Cystic Fibrosis Trust (https://www.cysticfibrosis.org.uk/) and the Medical Research Council Doctoral Training Partnership at Imperial (https://www.imperial.ac.uk/mrc-dtp-studentships). This work was partly supported by the Medical Research Council (MRC) for the MRC Centre for Environment and Health (MR/S019669/1), the National Institute for Health Research (NIHR) Health Protection Research Unit (HPRU) in Environmental Exposures and Health (NIHR200880) at Imperial College London, the NIHR HPRU in Chemical and Radiation Threats and Hazards (NIHR-200922) at Imperial College London and the NIRH HPRU in Environmental Exposures and Health at the University of Leicester (NIHR200901).

History

Author affiliation

Centre for Environmental Health and Sustainability

Version

  • VoR (Version of Record)

Published in

ENVIRONMENTAL HEALTH

Volume

21

Pagination

130

Publisher

BMC

issn

1476-069X

eissn

1476-069X

Copyright date

2022

Spatial coverage

England

Language

English