Development and validation of exhaled breath condensate microRNAs to identify and endotype asthma in children

• Published in: PloS one 2019-11, Vol.14 (11), p.e0224983-e0224983
• Main Authors: Mendes, Francisca Castro, Paciência, Inês, Ferreira, António Carlos, Martins, Carla, Rufo, João Cavaleiro, Silva, Diana, Cunha, Pedro, Farraia, Mariana, Moreira, Pedro, Delgado, Luís, Soares, Miguel Luz, Moreira, André
• Format: Article
• Language: English
• Subjects: Adolescent; Allergies; Asthma; Asthma - diagnosis; Asthma - genetics; Asthma - physiopathology; Biological markers; Biology and life sciences; Biomarkers; Breath Tests; Bronchodilation; Bronchodilators; Child; Childhood asthma; Children; Clusters; Condensates; Diagnosis; Exhalation; Female; Gene expression; Genetic Association Studies; Genetic Predisposition to Disease; Humans; Inflammation; Male; Mechanical engineering; Medical diagnosis; Medicine and Health Sciences; MicroRNA; MicroRNAs; MicroRNAs - genetics; miRNA; Nitric oxide; Nitric Oxide - analysis; Nitrogen oxides; Obesity; Pediatrics; Phenotype; Principal components analysis; Regression analysis; Regression models; Research and analysis methods; Reverse transcription; Schools; Skin; Skin tests; Spirometry; Surveys and Questionnaires
• ISSN: 1932-6203; 1932-6203
• DOI: 10.1371/journal.pone.0224983

Detection and quantification of microRNAs (miRNAs) in exhaled breath condensate (EBC) has been poorly explored. Therefore we aimed to assess miRNAs in EBC as potential biomarkers to diagnose and endotype asthma in school aged children. In a cross sectional, nested case control study, all the asthmatic children (n = 71) and a random sample of controls (n = 115), aged 7 to 12 years, attending 71 classrooms from 20 local schools were selected and arbitrarily allocated to the development or validation set. Participants underwent skin-prick testing, spirometry with bronchodilation, had exhaled level of nitric oxide determined and EBC collected. Based on previous studies eleven miRNAs were chosen and analyzed in EBC by reverse transcription-quantitative real-time PCR. Principal component analysis was applied to identify miRNAs profiles and associations were estimated using regression models. In the development set (n = 89) two clusters of miRNAs were identified. After adjustments, cluster 1 and three of its clustered miRNAs, miR-126-3p, miR-133a-3p and miR-145-5p were positively associated with asthma. Moreover miR-21-5p was negatively associated with symptomatic asthma and positively associated with positive bronchodilation without symptoms. An association was also found between miR-126-3p, cluster 2 and one of its clustered miRNA, miR-146-5p, with higher FEF25-75 reversibility. These findings were confirmed in the validation set (n = 97) where two identical clusters of miRNAs were identified. Additional significant associations were observed between miR-155-5p with symptomatic asthma, negative bronchodilation with symptoms and positive bronchodilation without symptoms. We showed that microRNAs can be measured in EBC of children and may be used as potential biomarkers of asthma, assisting asthma endotype establishment.