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Associations of wheezing phenotypes in the first six years of life with atopy, lung function and airway responsiveness in mid childhood.
  1. John Henderson (a.j.henderson{at}bris.ac.uk)
  1. University of Bristol, United Kingdom
    1. Raquel Granell (raquel.granell{at}bristol.ac.uk)
    1. University of Bristol, United Kingdom
      1. Jon Heron (jon.heron{at}bristol.ac.uk)
      1. University of Bristol, United Kingdom
        1. Andrea Sherriff (andrea.sherriff{at}bris.ac.uk)
        1. University of Bristol, United Kingdom
          1. Angela Simpson (angela.simpson{at}manchester.ac.uk)
          1. University of Manchester, United Kingdom
            1. Ashley A Woodcock (ashley.a.woodcock{at}man.ac.uk)
            1. University of Manchester, United Kingdom
              1. David P Strachan (sgjd950{at}sghms.ac.uk)
              1. St George's Hospital Medical School, United Kingdom
                1. Seif O Shaheen (s.shaheen{at}imperial.ac.uk)
                1. Imperial College, London, United Kingdom
                  1. Jonathan A C Sterne (jonathan.sterne{at}bristol.ac.uk)
                  1. University of Bristol, United Kingdom

                    Abstract

                    Background: Patterns of wheezing during early childhood may indicate differences in etiology and prognosis of respiratory illnesses. Improved characterization of wheezing phenotypes could lead to the identification of environmental influences on the development of asthma and airway diseases in predisposed individuals.

                    Methods: Data on 6,265 children from a longitudinal birth cohort (the ALSPAC study) with data collected on wheezing at seven time points from birth to seven years were analysed. Latent class analysis was used to assign phenotypes based on patterns of wheezing. Measures of atopy, airway function (FEV1, FEF25-75) and bronchial responsiveness were made at 7-9 years of age.

                    Results: Six phenotypes were identified. The strongest associations with atopy and airway responsiveness were found for intermediate onset (18 months) wheezing (OR for atopy 8.36, 95% CI 5.2-13.4; mean difference dose response to methacholine 1.76, 95% CI 1.41-2.12 %FEV1 per mmol, compared with infrequent/never wheeze phenotype). Late onset wheezing (after 42 months) was also associated with atopy (OR 6.6, 95% CI 4.7-9.4) and airway responsiveness (mean difference 1.61, 95% CI 1.37-1.85 %FEV1 per mmol). Transient and prolonged early wheeze were not associated with atopy but were weakly associated with increased airway responsiveness and persistent wheeze had intermediate associations with these outcomes.

                    Conclusions: The wheezing phenotypes most strongly associated with atopy and airway responsiveness were characterised by onset after age 18 months. This has potential implications for the timing of environmental influences on the initiation of atopic wheezing in early childhood.

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