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A methodology to establish a database to study gene environment interactions for childhood asthma

BACKGROUND: Gene-environment interactions are likely to explain some of the heterogeneity in childhood asthma. Here, we describe the methodology and experiences in establishing a database for childhood asthma designed to study gene-environment interactions (PAGES - Paediatric Asthma Gene Environment...

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Detalles Bibliográficos
Autores principales: Turner, Stephen W, Ayres, Jon G, Macfarlane, Tatiana V, Mehta, Anil, Mehta, Gita, Palmer, Colin N, Cunningham, Steve, Adams, Tim, Aniruddhan, Krishnan, Bell, Claire, Corrigan, Donna, Cunningham, Jason, Duncan, Andrew, Hunt, Gerard, Leece, Richard, MacFadyen, Una, McCormick, Jonathan, McLeish, Sally, Mitra, Andrew, Miller, Deborah, Waxman, Elizabeth, Webb, Alan, Wojcik, Slawomir, Mukhopadhyay, Somnath, Macgregor, Donald
Formato: Texto
Lenguaje:English
Publicado: BioMed Central 2010
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC3019209/
https://www.ncbi.nlm.nih.gov/pubmed/21134251
http://dx.doi.org/10.1186/1471-2288-10-107
Descripción
Sumario:BACKGROUND: Gene-environment interactions are likely to explain some of the heterogeneity in childhood asthma. Here, we describe the methodology and experiences in establishing a database for childhood asthma designed to study gene-environment interactions (PAGES - Paediatric Asthma Gene Environment Study). METHODS: Children with asthma and under the care of a respiratory paediatrician are being recruited from 15 hospitals between 2008 and 2011. An asthma questionnaire is completed and returned by post. At a routine clinic visit saliva is collected for DNA extraction. Detailed phenotyping in a proportion of children includes spirometry, bronchodilator response (BDR), skin prick reactivity, exhaled nitric oxide and salivary cotinine. Dietary and quality of life questionnaires are completed. Data are entered onto a purpose-built database. RESULTS: To date 1045 children have been invited to participate and data collected in 501 (48%). The mean age (SD) of participants is 8.6 (3.9) years, 57% male. DNA has been collected in 436 children. Spirometry has been obtained in 172 children, mean % predicted (SD) FEV(1 )97% (15) and median (IQR) BDR is 5% (2, 9). There were differences in age, socioeconomic status, severity and %FEV(1 )between the different centres (p≤0.024). Reasons for non-participation included parents not having time to take part, children not attending clinics and, in a small proportion, refusal to take part. CONCLUSIONS: It is feasible to establish a national database to study gene-environment interactions within an asthmatic paediatric population; there are barriers to participation and some different characteristics in individuals recruited from different centres. Recruitment to our study continues and is anticipated to extend current understanding of asthma heterogeneity.