The mediating effect of immune markers on the association between ambient air pollution and adult-onset asthma

Nahid Mostafavi, Ayoung Jeong, Jelle Vlaanderen, Medea Imboden, Paolo Vineis, Debbie Jarvis, Manolis Kogevinas, Nicole Probst-Hensch, Roel Vermeulen*

*Corresponding author for this work

    Research output: Contribution to journalArticlepeer-review

    19 Citations (Scopus)

    Abstract

    We aim to investigate to what extent a set of immune markers mediate the association between air pollution and adult-onset asthma. We considered long-term exposure to multiple air pollution markers and a panel of 13 immune markers in peripheral blood samples collected from 140 adult cases and 199 controls using a nested-case control design. We tested associations between air pollutants and immune markers and adult-onset asthma using mixed-effects (logistic) regression models, adjusted for confounding variables. In order to evaluate a possible mediating effect of the full set of immune markers, we modelled the relationship between asthma and air pollution with a partial least square path model. We observed a strong positive association of IL-1RA [OR 1.37; 95% CI (1.09, 1.73)] with adult-onset asthma. Univariate models did not yield any association between air pollution and immune markers. However, mediation analyses indicated that 15% of the effect of air pollution on risk of adult-onset asthma was mediated through the immune system when considering all immune markers as a latent variable (path coefficient (β) = 0.09; 95% CI: (−0.02, 0.20)). This effect appeared to be stronger for allergic asthma (22%; β = 0.12; 95% CI: (−0.03, 0.27)) and overweight subjects (27%; β = 0.19; 95% CI: (−0.004, 0.38)). Our results provides supportive evidence for a mediating effect of the immune system in the association between air pollution and adult-onset asthma.

    Original languageEnglish
    Article number8818
    JournalScientific Reports
    Volume9
    Issue number1
    DOIs
    Publication statusPublished - 1 Dec 2019

    Bibliographical note

    Funding Information:
    This research has received funding from the European Community’s Seventh Framework Program (FP7/2007e2011) under Grant Agreement Number: 308610 (Exposomics). The SAPALDIA cohort and biobank is funded by Swiss National Science Foundation Grant Number: 33CS30-148470/1&2 to NPH. The authors thank George Downward for language editing of this manuscript.

    Publisher Copyright:
    © 2019, The Author(s).

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