Title: | Exhaled biomarkers and gene expression at preschool age improve asthma prediction at 6 years of age |
Author(s): | Klaassen EM; van de Kant KD; Jobsis Q; van Schayck OC; Smolinska A; Dallinga JW; van Schooten FJ; den Hartog GJ; de Jongste JC; Rijkers GT; Dompeling E; |
Address: | 1 Department of Pediatric Pulmonology and |
Journal Title: | Am J Respir Crit Care Med |
DOI: | 10.1164/rccm.201408-1537OC |
ISSN/ISBN: | 1535-4970 (Electronic) 1073-449X (Linking) |
Abstract: | "RATIONALE: A reliable asthma diagnosis is difficult in wheezing preschool children. OBJECTIVES: To assess whether exhaled biomarkers, expression of inflammation genes, and early lung function measurements can improve a reliable asthma prediction in preschool wheezing children. METHODS: Two hundred two preschool recurrent wheezers (aged 2-4 yr) were prospectively followed up until 6 years of age. At 6 years of age, a diagnosis (asthma or transient wheeze) was based on symptoms, lung function, and asthma medication use. The added predictive value (area under the receiver operating characteristic curve [AUC]) of biomarkers to clinical information (assessed with the Asthma Predictive Index [API]) assessed at preschool age in diagnosing asthma at 6 years of age was determined with a validation set. Biomarkers in exhaled breath condensate, exhaled volatile organic compounds (VOCs), gene expression, and airway resistance were measured. MEASUREMENTS AND MAIN RESULTS: At 6 years of age, 198 children were diagnosed (76 with asthma, 122 with transient wheeze). Information on exhaled VOCs significantly improved asthma prediction (AUC, 89% [increase of 28%]; positive predictive value [PPV]/negative predictive value [NPV], 82/83%), which persisted in the validation set. Information on gene expression of toll-like receptor 4, catalase, and tumor necrosis factor-alpha significantly improved asthma prediction (AUC, 75% [increase of 17%]; PPV/NPV, 76/73%). This could not be confirmed after validation. Biomarkers in exhaled breath condensate and airway resistance (pre- and post- bronchodilator) did not improve an asthma prediction. The combined model with VOCs, gene expression, and API had an AUC of 95% (PPV/NPV, 90/89%). CONCLUSIONS: Adding information on exhaled VOCs and possibly expression of inflammation genes to the API significantly improves an accurate asthma diagnosis in preschool children. Clinical trial registered with www.clinicaltrial.gov (NCT 00422747)" |
Keywords: | "Airway Resistance/genetics/physiology Asthma/*diagnosis/genetics/physiopathology Biomarkers/metabolism *Breath Tests Catalase/blood/genetics Child Child, Preschool Diagnosis, Differential Female Gene Expression Profiling/*methods Humans Inflammation/*diag;" |
Notes: | "MedlineKlaassen, Ester M M van de Kant, Kim D G Jobsis, Quirijn van Schayck, Onno C P Smolinska, Agnieszka Dallinga, Jan W van Schooten, Frederik J den Hartog, Gertjan J M de Jongste, Johan C Rijkers, Ger T Dompeling, Edward eng Clinical Trial Research Support, Non-U.S. Gov't 2014/12/05 Am J Respir Crit Care Med. 2015 Jan 15; 191(2):201-7. doi: 10.1164/rccm.201408-1537OC" |