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| Title: | Prediction of asthma in symptomatic preschool children using exhaled nitric oxide, Rint and specific IgE. |
| Author(s): | Caudri, D. Wijga, A.H. Hoekstra, M.O. Kerkhof, M. van de Koppelman, G.H. Brunekreef, B. Smit, H.A. Jongste, J.C. de |
| Publication year: | 2010 |
| Document type: | Article / Letter to editor |
| Journal: | Thorax |
| ISSN: | 0040-6376 |
| Volume: | vol. 65 |
| Issue: | iss. 9 |
| Start page: | p. 801 |
| End page: | p. 807 |
| Abstract: | RATIONALE: For clinicians it remains very difficult to predict whether preschool children with symptoms suggestive of asthma will develop asthma in later childhood. OBJECTIVE: To investigate whether measurement of fraction of exhaled nitric oxide (FE(NO)), interrupter resistance (Rint) or specific immunoglobulin E (IgE) in 4-year-old children with suggestive symptoms can predict asthma symptoms up to age 8 years. METHODS: Children were recruited from the PIAMA birth cohort. All children with symptoms suggestive of asthma at age 3 or 4 years, who were invited for medical examination at age 4 (n=848), were eligible. Associations of FE(NO) (n=308), Rint (n=482) and specific IgE (n=380) at 4 years with wheezing and asthma at the ages of 5-8 years were assessed using repeated measurement analyses. The added predictive value of these objective tests was then investigated by including parameters for clinical history in the model. RESULTS: FE(NO) and specific IgE measured at 4 years were associated with wheezing and asthma at 8 years. Both tests also remained significant predictors after mutual adjustment and adjustment for clinical history: OR on wheezing at 8 years for FE(NO) ((10)log-scale, per IQR) 1.6 (95% CI 1.1 to 2.2) and for specific IgE 2.8 (95% CI 1.9 to 4.1). Rint was significantly associated with wheezing at age 6, but not at 7 and 8 years. CONCLUSIONS: In preschool children with symptoms suggestive of asthma, both FE(NO) and specific IgE measured at age 4, but not Rint, improved the prediction of asthma symptoms until the age of 8 years, independent of clinical history. |
| Subject: | IGMD 3: Genomic disorders and inherited multi-system disorders |
| Organization: | UMCN Extern Paediatrics |
| Appears in Collections: | Academic bibliography
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Please use this identifier to cite or link to this item:
http://hdl.handle.net/2066/89694
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