Open AccessQuantification of atopy, lung function and airway hypersensitivity in adults
Author(s) -
Marinho Susana,
Simpson Angela,
Marsden Paul,
Smith Jacky A,
Custovic Adnan
Publication year - 2011
Publication title -
clinical and translational allergy
Language(s) - English
Resource type - Journals
SCImago Journal Rank - 0.979
H-Index - 37
ISSN - 2045-7022
DOI - 10.1186/2045-7022-1-16
Subject(s) - medicine , atopy , lung function , allergy , immunology , respiratory hypersensitivity , airway , lung , dermatology , anesthesia
Background Studies in children have shown that concentration of specific serum IgE (sIgE) and size of skin tests to inhalant allergens better predict wheezing and reduced lung function than the information on presence or absence of atopy. However, very few studies in adults have investigated the relationship of quantitative atopy with lung function and airway hyperresponsiveness (AHR). Objective To determine the association between lung function and AHR and quantitative atopy in a large sample of adults from the UK. Methods FEV 1 and FVC (% predicted) were measured using spirometry and airway responsiveness by methacholine challenge (5‐breath dosimeter protocol) in 983 subjects (random sample of 800 parents of children enrolled in a population‐based birth cohort enriched with 183 patients with physician‐diagnosed asthma). Atopic status was assessed by skin prick tests (SPT) and measurement of sIgE (common inhalant allergens). We also measured indoor allergen exposure in subjects' homes. Results Spirometry was completed by 792 subjects and 626 underwent methacholine challenge, with 100 (16.0%) having AHR (dose‐response slope>25). Using sIgE as a continuous variable in a multiple linear regression analysis, we found that increasing levels of sIgE to mite, cat and dog were significantly associated with lower FEV 1 (mite p = 0.001, cat p = 0.0001, dog p = 2.95 × 10 ‐8 ). Similar findings were observed when using the size of wheal on skin testing as a continuous variable, with significantly poorer lung function with increasing skin test size (mite p = 8.23 × 10 ‐8 , cat p = 3.93 × 10 ‐10 , dog p = 3.03 × 10 ‐15 , grass p = 2.95 × 10 ‐9 ). The association between quantitative atopy with lung function and AHR remained unchanged when we repeated the analyses amongst subjects defined as sensitised using standard definitions (sIgE>0.35 kUa/l, SPT‐3 mm>negative control). Conclusions In the studied population, lung function decreased and AHR increased with increasing sIgE levels or SPT wheal diameter to inhalant allergens, suggesting that atopy may not be a dichotomous outcome influencing lung function and AHR.