DNA methylation profiles between airway epithelium and proxy tissues in children. (18th September 2017)

• Record Type: Journal Article
• Authors: Brugha, Rossa; Lowe, Robert; Henderson, A. John; Holloway, John W.; Rakyan, Vardhman; Wozniak, Eva; Mahmud, Nadiya; Seymour, Kay; Grigg, Jonathan; Shaheen, Seif O.
• Is Part Of: Acta pædiatrica. Volume 106:Number 12(2017)
• Page Start: 2011
• Page End: 2016
• Publication Date: 2017-09-18
• Subjects: Asthma and early wheeze -- Epigenetics; Pediatrics -- Periodicals; Pediatrics; 618.92
• DOI: 10.1111/apa.14027
• Languages: English
• ISSNs: 0803-5253

Abstract

Abstract: Aim: Epidemiological studies of deoxyribonucleic acid (DNA) methylation in airway disease have largely been conducted using blood or buccal samples. However, given tissue specificity of DNA methylation, these surrogate tissues may not allow reliable inferences about methylation in the lung. We sought to compare the pattern of DNA methylation in blood, buccal and nasal epithelial cells to that in airway epithelial cells from children. Methods: Samples of blood, and buccal, nasal and airway epithelium were obtained from six children undergoing elective anaesthesia for adenotonsillectomy. DNA methylation was assessed at 450 000 5′‐C—phosphate—G‐3′ (CpG) sites using the Illumina HumanMethylation450 array. Results: Eighteen samples from all sites were suitable for analysis. Hierarchical clustering demonstrated that the methylation profile in nasal epithelium was most representative of that in airway epithelium; the profile in buccal cells was moderately similar and that in blood was least similar. Conclusion: DNA methylation in blood poorly reflects methylation in airway epithelium. Future epidemiological studies of DNA methylation and airway diseases should consider measurement of methylation either in buccal cells or, preferably, in nasal epithelial cells.