Epigenome-wide association study of rheumatoid arthritis identifies differentially methylated loci in B cells

Epigenetic regulation of immune cell types could be critical for the development and maintenance of autoimmune diseases like rheumatoid arthritis (RA). B cells are highly relevant in RA, since patients express autoantibodies and depleting this cell type is a successful therapeutic approach. Epigenet...

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Veröffentlicht in:Human molecular genetics 2017-07, Vol.26 (14), p.2803-2811
Hauptverfasser: Julià, Antonio, Absher, Devin, López-Lasanta, María, Palau, Nuria, Pluma, Andrea, Waite Jones, Lindsay, Glossop, John R, Farrell, William E, Myers, Richard M, Marsal, Sara
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Sprache:eng
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Zusammenfassung:Epigenetic regulation of immune cell types could be critical for the development and maintenance of autoimmune diseases like rheumatoid arthritis (RA). B cells are highly relevant in RA, since patients express autoantibodies and depleting this cell type is a successful therapeutic approach. Epigenetic variation, such as DNA methylation, may mediate the pathogenic activity of B cells. In this study, we performed an epigenome-wide association study (EWAS) for RA with three different replication cohorts, to identify disease-specific alterations in DNA methylation in B cells. CpG methylation in isolated B lymphocytes was assayed on the Illumina HumanMethylation450 BeadChip in a discovery cohort of RA patients (N = 50) and controls (N = 75). Differential methylation was observed in 64 CpG sites (q 
ISSN:0964-6906
1460-2083
DOI:10.1093/hmg/ddx177