Identification of Cell‐Specific Differential DNA Methylation Associated With Methotrexate Treatment Response in Rheumatoid Arthritis

Author:

Adams Cameron1ORCID,Nair Nisha2,Plant Darren3,Verstappen Suzanne M. M.4,Quach Hong L.1,Quach Diana L.1,Carvidi Alex5,Nititham Joanne6,Nakamura Mary7,Graf Jonathan5,Barton Anne3,Criswell Lindsey A.6,Barcellos Lisa F.8ORCID

Affiliation:

1. School of Public Health, University of California Berkeley

2. Centre of Genetics and Genomics Versus Arthritis, Manchester Academic Health Sciences Centre, The University of Manchester Manchester UK

3. Centre of Genetics and Genomics Versus Arthritis, Manchester Academic Health Sciences Centre, NIHR Manchester BRC, Manchester University Foundation Trust, The University of Manchester Manchester UK

4. NIHR Manchester BRC, Manchester University Foundation Trust, and Centre for Epidemiology Versus Arthritis, Division of Musculoskeletal and Dermatological Sciences, Manchester Academic Health Sciences Centre, The University of Manchester, Manchester, UK, Institute of Cellular Medicine, Newcastle University, and NIHR Newcastle BRC, Newcastle upon Tyne Hospitals NHS Foundation Trust Newcastle upon Tyne UK

5. University of California San Francisco

6. National Human Genome Research Institute, NIH Bethesda Maryland

7. University of California and San Francisco Veterans Administration Health System San Francisco California

8. School of Public Health, University of California, Berkeley, and National Human Genome Research Institute, NIH Bethesda Maryland

Abstract

ObjectiveWe undertook this study to estimate changes in cell‐specific DNA methylation (DNAm) associated with methotrexate (MTX) response using whole blood samples collected from rheumatoid arthritis (RA) patients before and after initiation of MTX treatment.MethodsPatients included in this study were from the Rheumatoid Arthritis Medication Study (n = 66) and the University of California San Francisco Rheumatoid Arthritis study (n = 11). All patients met the American College of Rheumatology RA classification criteria. Blood samples were collected at baseline and following treatment. Disease Activity Scores in 28 joints using the C‐reactive protein level were collected at baseline and after 3–6 months of treatment with MTX. Methylation profiles were generated using the Illumina Infinium HumanMethylation450 and MethylationEPIC v1.0 BeadChip arrays using DNA from whole blood. MTX response was defined using the EULAR response criteria (responders showed good/moderate response; nonresponders showed no response). Differentially methylated positions were identified using the Limma software package and Tensor Composition Analysis, which is a method for identifying cell‐specific differential DNAm at the CpG level from tissue‐level (“bulk”) data. Differentially methylated regions were identified using Comb‐p software.ResultsWe found evidence of differential global methylation between treatment response groups. Further, we found patterns of cell‐specific differential global methylation associated with MTX response. After correction for multiple testing, 1 differentially methylated position was associated with differential DNAm between responders and nonresponders at baseline in CD4+ T cells, CD8+ T cells, and natural killer cells. Thirty‐nine cell‐specific differentially methylated regions associated with MTX treatment response were identified. There were no significant findings in analyses of whole blood samples.ConclusionWe identified cell‐specific changes in DNAm that were associated with MTX treatment response in RA patients. Future studies of DNAm and MTX treatment response should include measurements of DNAm from sorted cells.image

Funder

National Institute of Arthritis and Musculoskeletal and Skin Diseases

National Institute of Neurological Disorders and Stroke

Rheumatology Research Foundation

Versus Arthritis

Publisher

Wiley

Subject

Immunology,Rheumatology,Immunology and Allergy

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