Traffic-related air pollution exposure is associated with allergic sensitization, asthma, and poor lung function in middle age

Gayan Bowatte, Caroline J. Lodge, Luke D. Knibbs, Adrian J. Lowe, Bircan Erbas, Martine Dennekamp, Guy B. Marks, Graham G. Giles, Stephen Morrison, Bruce Thompson, Paul S. Thomas, Jennie Hui, Jennifer L. Perret, Michael J. Abramson, E. Haydn Walters, Melanie C. Matheson, Shyamali C. Dharmage

Research output: Contribution to journalArticle

47 Citations (Scopus)

Abstract

Background Traffic-related air pollution (TRAP) exposure is associated with allergic airway diseases and reduced lung function in children, but evidence concerning adults, especially in low-pollution settings, is scarce and inconsistent. Objectives We sought to determine whether exposure to TRAP in middle age is associated with allergic sensitization, current asthma, and reduced lung function in adults, and whether these associations are modified by variants in Glutathione S-Transferase genes. Methods The study sample comprised the proband 2002 laboratory study of the Tasmanian Longitudinal Health Study. Mean annual residential nitrogen dioxide (NO2) exposure was estimated for current residential addresses using a validated land-use regression model. Associations between TRAP exposure and allergic sensitization, lung function, current wheeze, and asthma (n = 1405) were investigated using regression models. Results Increased mean annual NO2 exposure was associated with increased risk of atopy (adjusted odds ratio [aOR], 1.14; 95% CI, 1.02-1.28 per 1 interquartile range increase in NO2 [2.2 ppb]) and current wheeze (aOR, 1.14; 1.02-1.28). Similarly, living less than 200 m from a major road was associated with current wheeze (aOR, 1.38; 95% CI, 1.06-1.80) and atopy (aOR, 1.26; 95% CI, 0.99-1.62), and was also associated with having significantly lower prebronchodilator and postbronchodilator FEV1 and prebronchodilator forced expiratory flow at 25% to 75% of forced vital capacity. We found evidence of interactions between living less than 200 m from a major road and GSTT1 polymorphism for atopy, asthma, and atopic asthma. Overall, carriers of the GSTT1 null genotype had an increased risk of asthma and allergic outcomes if exposed to TRAP. Conclusions Even relatively low TRAP exposures confer an increased risk of adverse respiratory and allergic outcomes in genetically susceptible individuals.

Original languageEnglish
Pages (from-to)122-129
JournalJournal of Allergy and Clinical Immunology
Volume139
Issue number1
Early online date24 May 2016
DOIs
Publication statusPublished - 1 Jan 2017

    Fingerprint

Cite this