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Built environment factors predictive of early rapid lung function decline in cystic fibrosis.
Gecili, Emrah; Brokamp, Cole; Rasnick, Erika; Afonso, Pedro M; Andrinopoulou, Eleni-Rosalina; Dexheimer, Judith W; Clancy, John P; Keogh, Ruth H; Ni, Yizhao; Palipana, Anushka; Pestian, Teresa; Vancil, Andrew; Zhou, Grace C; Su, Weiji; Siracusa, Christopher; Ryan, Patrick; Szczesniak, Rhonda D.
Afiliación
  • Gecili E; Division of Biostatistics & Epidemiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Brokamp C; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA.
  • Rasnick E; Division of Biostatistics & Epidemiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Afonso PM; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA.
  • Andrinopoulou ER; Division of Biostatistics & Epidemiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Dexheimer JW; Department of Biostatistics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Clancy JP; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Keogh RH; Department of Biostatistics, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Ni Y; Department of Epidemiology, Erasmus Medical Center, Rotterdam, The Netherlands.
  • Palipana A; Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Pestian T; Division of Emergency Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Vancil A; Department of Pediatrics, University of Cincinnati, Cincinnati, Ohio, USA.
  • Zhou GC; Division of Pulmonary Medicine, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Su W; Cystic Fibrosis Foundation, Bethesda, Maryland, USA.
  • Siracusa C; London School of Hygiene and Tropical Medicine, London, UK.
  • Ryan P; Division of Biomedical Informatics, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
  • Szczesniak RD; Division of Biostatistics & Epidemiology, Cincinnati Children's Hospital Medical Center, Cincinnati, Ohio, USA.
Pediatr Pulmonol ; 58(5): 1501-1513, 2023 05.
Article en En | MEDLINE | ID: mdl-36775890
BACKGROUND: The extent to which environmental exposures and community characteristics of the built environment collectively predict rapid lung function decline, during adolescence and early adulthood in cystic fibrosis (CF), has not been examined. OBJECTIVE: To identify built environment characteristics predictive of rapid CF lung function decline. METHODS: We performed a retrospective, single-center, longitudinal cohort study (n = 173 individuals with CF aged 6-20 years, 2012-2017). We used a stochastic model to predict lung function, measured as forced expiratory volume in 1 s (FEV1 ) of % predicted. Traditional demographic/clinical characteristics were evaluated as predictors. Built environmental predictors included exposure to elemental carbon attributable to traffic sources (ECAT), neighborhood material deprivation (poverty, education, housing, and healthcare access), greenspace near the home, and residential drivetime to the CF center. MEASUREMENTS AND MAIN RESULTS: The final model, which included ECAT, material deprivation index, and greenspace, alongside traditional demographic/clinical predictors, significantly improved fit and prediction, compared with only demographic/clinical predictors (Likelihood Ratio Test statistic: 26.78, p < 0.0001; the difference in Akaike Information Criterion: 15). An increase of 0.1 µg/m3 of ECAT was associated with 0.104% predicted/yr (95% confidence interval: 0.024, 0.183) more rapid decline. Although not statistically significant, material deprivation was similarly associated (0.1-unit increase corresponded to additional decline of 0.103% predicted/year [-0.113, 0.319]). High-risk regional areas of rapid decline and age-related heterogeneity were identified from prediction mapping. CONCLUSION: Traffic-related air pollution exposure is an important predictor of rapid pulmonary decline that, coupled with community-level material deprivation and routinely collected demographic/clinical characteristics, enhance CF prognostication and enable personalized environmental health interventions.
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Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrosis Quística Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Humans Idioma: En Revista: Pediatr Pulmonol Asunto de la revista: PEDIATRIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos

Texto completo: 1 Colección: 01-internacional Banco de datos: MEDLINE Asunto principal: Fibrosis Quística Tipo de estudio: Etiology_studies / Incidence_studies / Observational_studies / Prognostic_studies / Risk_factors_studies Límite: Adolescent / Adult / Humans Idioma: En Revista: Pediatr Pulmonol Asunto de la revista: PEDIATRIA Año: 2023 Tipo del documento: Article País de afiliación: Estados Unidos