John R. Glossop
Genome-wide profiling in treatment-naive early rheumatoid arthritis reveals DNA methylome changes in T and B lymphocytes
Glossop, John R.; Emes, Richard D.; Nixon, Nicola B.; Packham, Jon C.; Fryer, Anthony A.; Mattey, Derek L.; Farrell, William E.
Authors
Richard D. Emes
Nicola B. Nixon
Jon C. Packham
Professor Anthony Fryer a.a.fryer@keele.ac.uk
Derek L. Mattey
William E. Farrell
Abstract
Aim: Although aberrant DNA methylation has been described in rheumatoid arthritis (RA), no studies have interrogated this epigenetic modification in early disease. Following recent investigations of T and B lymphocytes in established disease, we now characterize in these cell populations genome-wide DNA methylation in treatment-naive patients with early RA. Patients & methods: HumanMethylation450 BeadChips were used to examine genome-wide DNA methylation in lymphocyte populations from 23 early RA patients and 11 healthy individuals. Results: Approximately 2000 CpGs in each cell type were differentially methylated in early RA. Clustering analysis identified a novel methylation signature in each cell type (150 sites in T lymphocytes, 113 sites in B lymphocytes) that clustered all patients separately from controls. A subset of sites differentially methylated in early RA displayed similar changes in established disease. Conclusion: Treatment-naive early RA patients display novel disease-specific DNA methylation aberrations, supporting a potential role for these changes in the development of RA.
Citation
Glossop, J. R., Emes, R. D., Nixon, N. B., Packham, J. C., Fryer, A. A., Mattey, D. L., & Farrell, W. E. (2016). Genome-wide profiling in treatment-naive early rheumatoid arthritis reveals DNA methylome changes in T and B lymphocytes. Epigenomics, 8(2), 209-224. https://doi.org/10.2217/epi.15.103
Journal Article Type | Article |
---|---|
Online Publication Date | Nov 10, 2015 |
Publication Date | 2016 |
Deposit Date | Aug 24, 2023 |
Journal | EPIGENOMICS |
Print ISSN | 1750-1911 |
Publisher | Future Medicine |
Peer Reviewed | Peer Reviewed |
Volume | 8 |
Issue | 2 |
Pages | 209-224 |
DOI | https://doi.org/10.2217/epi.15.103 |
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