| Literature DB >> 31221806 |
Christer Janson1,2, Andrei Malinovschi3, Andre F S Amaral2, Simone Accordini4, Jean Bousquet5,6,7, A Sonia Buist8, Giorgio Walter Canonica9, Barbro Dahlén10, Judith Garcia-Aymerich11,12,13, Louisa Gnatiuc14, Marek L Kowalski15, Jaymini Patel2, Wan Tan16, Kjell Torén17, Torsten Zuberbier7, Peter Burney2, Deborah Jarvis2.
Abstract
Bronchodilator response (BDR) testing is used as a diagnostic method in obstructive airway diseases. The aim of this investigation was to compare different methods for measuring BDR in participants with asthma and chronic obstructive pulmonary disease (COPD) and to study to the extent to which BDR was related to symptom burden and phenotypic characteristics.Forced expiratory volume in 1 s (FEV1) and forced vital capacity (FVC) were measured before and 15 min after 200 μg of salbutamol in 35 628 subjects aged ≥16 years from three large international population studies. The subjects were categorised in three groups: current asthma (n=2833), COPD (n=1146) and no airway disease (n=31 649). Three definitions for flow-related reversibility (increase in FEV1) and three for volume-related reversibility (increase in FVC) were used.The prevalence of bronchodilator reversibility expressed as increase FEV1 ≥12% and 200 mL was 17.3% and 18.4% in participants with asthma and COPD, respectively, while the corresponding prevalence was 5.1% in those with no airway disease. In asthma, bronchodilator reversibility was associated with wheeze (OR 1.36, 95% CI 1.04-1.79), atopy (OR 1.36, 95% CI 1.04-1.79) and higher exhaled nitric oxide fraction, while in COPD neither flow- nor volume-related bronchodilator reversibility was associated with symptom burden, exacerbations or health status after adjusting for pre-bronchodilator FEV1Bronchodilator reversibility was at least as common in participants with COPD as those with asthma. This indicates that measures of reversibility are of limited value for distinguishing asthma from COPD in population studies. However, in asthma, bronchodilator reversibility may be a phenotypic marker.Entities:
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Year: 2019 PMID: 31221806 DOI: 10.1183/13993003.00561-2019
Source DB: PubMed Journal: Eur Respir J ISSN: 0903-1936 Impact factor: 16.671