Pre-defined gene co-expression modules in rheumatoid arthritis transition towards molecular health following anti-TNF therapy

Author:

Sutcliffe Megan1,Nair Nisha12ORCID,Oliver James12,Morgan Ann W3,Isaacs John D4,Wilson Anthony G5,Verstappen Suzanne M M26,Viatte Sebastien127,Hyrich Kimme L26ORCID,Morris Andrew P1,Barton Anne12ORCID,Plant Darren12ORCID

Affiliation:

1. Versus Arthritis Centre for Genetics and Genomics, Division of Musculoskeletal Sciences, The University of Manchester

2. NIHR Manchester Biomedical Research Centre, Manchester University NHS Foundation Trust, Manchester Academic Health Sciences Centre , Manchester

3. School of Medicine, University of Leeds & NIHR Leeds Biomedical Research Centre and NIHR In Vitro Diagnostic Co-operative, Leeds Teaching Hospitals NHS Trust, University of Leeds , Leeds

4. Translational & Clinical Research Institution, Newcastle University & Musculoskeletal Unit, Newcastle upon Tyne Hospitals NHS Foundation Trust, Newcastle University , Newcastle upon Tyne, UK

5. School of Medicine & Medical Science, Conway Institute, University College Dublin , Bellfield, Dublin 4, Ireland

6. Versus Arthritis Centre for Epidemiology, Centre for Musculoskeletal Research

7. Lydia Becker Institute of Immunology and Inflammation, Faculty of Biology, Medicine and Health, The University of Manchester , Manchester, UK

Abstract

Abstract Background No reliable biomarkers to predict response to TNF inhibitors (TNFi) in RA patients currently exist. The aims of this study were to replicate changes in gene co-expression modules that were previously reported in response to TNFi therapy in RA; to test if changes in module expression are specific to TNFi therapy; and to determine whether module expression transitions towards a disease-free state in responding patients. Method Published transcriptomic data from the whole blood of disease-free controls (n = 10) and RA patients, treated with the TNFi adalimumab (n = 70) or methotrexate (n = 85), were studied. Treatment response was assessed using the EULAR response criteria following 3 or 6 months of treatment. Change in transcript expression between pre- and post-treatment was recorded for previously defined modules. Linear mixed models tested whether modular expression after treatment transitioned towards a disease-free state. Results For 25 of the 27 modules, change in expression between pre- and post-treatment in the adalimumab cohort replicated published findings. Of these 25 modules, six transitioned towards a disease-free state by 3 months (P < 0.05), irrespective of clinical response. One module (M3.2), related to inflammation and TNF biology, significantly correlated with response to adalimumab. Similar patterns of modular expression, with reduced magnitude, were observed in the methotrexate cohort. Conclusion This study provides independent validation of changes in module expression in response to therapy in RA. However, these effects are not specific to TNFi. Further studies are required to determine whether specific modules could assist molecular classification of therapeutic response.

Funder

Research into Inflammatory Arthritis Centre Versus Arthritis

National Institute for Health Research

Newcastle Biomedical Research Centre

Department of Health and Social Care

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

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