Annals of the Rheumatic Diseases
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The Annals of the Rheumatic Diseases is a peer-reviewed medical journal. It is co-owned by the BMJ Group and the European League Against Rheumatism and covers all aspects of rheumatology, including musculoskeletal conditions, arthritis, and connective tissue diseases. The journal publishes basic, clinical, and translational research and abstracts from conferences. The journal was established in 1939. It is available online by subscription and archived editions of the journal (older than one year) are available free of charge. Each issue, the editor-in-chief selects a paper to be published open access as an "Editors Choice". The editor-in-chief is Tore K. Kvien. Source
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| Language | English |
| Country | United Kingdom |
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Recent Articles
Search Articles2019 European League Against Rheumatism/American College of Rheumatology classification criteria for systemic lupus erythematosus
Discussion New SLE classification criteria were developed with support by both the ACR and EULAR. Through a four-phase, iterative process, we have defined an additive, weighted multicriteria system that produces a measure of the relative probability that an individual can be classified as SLE. The system defines a threshold above which experts would classify cases as SLE for the purpose of research studies.
Treating axial spondyloarthritis and peripheral spondyloarthritis, especially psoriatic arthritis, to target: 2017 update of recommendations by an international task force
The treatment target should be clinical remission/inactive disease of musculoskeletal (arthritis, dactylitis, enthesitis, axial disease) and extra-articular manifestations. This bullet point previously read: ‘A major treatment target should be clinical remission/inactive disease of musculoskeletal involvement (arthritis, dactylitis, enthesitis, axial disease), taking extra-articular manifestations into consideration’.
2024 EULAR points to consider on the initiation of targeted therapies in patients with inflammatory arthritis and a history of cancer
Discussion The EULAR Task Force formulated five OPS and eight PTC relevant to the initiation of targeted therapies in patients with IA and a history of cancer. Seven out of eight PTC concern patients in cancer remission. PTC 8 concerns patients not in cancer remission.
2024 EULAR points to consider on the initiation of targeted therapies in patients with inflammatory arthritis and a history of cancer
Discussion The EULAR Task Force formulated five OPS and eight PTC relevant to the initiation of targeted therapies in patients with IA and a history of cancer. Seven out of eight PTC concern patients in cancer remission. PTC 8 concerns patients not in cancer remission.
Systematic literature review and meta-analysis informing the EULAR points to consider on the initiation of targeted therapies in patients with inflammatory arthritis and a history of cancer
Systematic literature review and meta-analysis informing the EULAR points to consider on the initiation of targeted therapies in patients with inflammatory arthritis and a history of cancer Statistics from Altmetric.com Request Permissions If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.
Expert consensus recommendations for the diagnosis and treatment of chronic non-bacterial osteitis (CNO) in adults
Conclusions and future perspectives This international initiative developed a first consensus statement regarding the disease definition of adults with SBI. It was agreed by the panel collectively to label this disease spectrum as CNO in adults (adult CNO), and no longer use terms like SAPHO syndrome, SCCH, PAO and CRMO. Building on this shared definition and name, the panel developed a first set of multidisciplinary consensus recommendations for diagnosis and treatment of adult CNO.
Ivarmacitinib, a selective Janus kinase 1 inhibitor, in patients with moderate-to-severe active rheumatoid arthritis and inadequate response to conventional synthetic DMARDs: results from a phase III randomised clinical trial
Abstract Objective To assess the efficacy/safety of ivarmacitinib, a selective Janus kinase (JAK) 1 inhibitor, in patients with moderate-to-severe active rheumatoid arthritis (RA) who had an inadequate response to conventional synthetic disease-modifying antirheumatic drugs (csDMARDs). Methods Patients were randomised (1:1:1) to receive either placebo (n=188), ivarmacitinib 4 mg (n=189) or ivarmacitinib 8 mg (n=189) once daily, with background csDMARDs allowed.
Correction: Olokizumab plus methotrexate: safety and efficacy over 106 weeks of treatment
Feist E, Fleischmann RM, Fatenejad S, et al. Olokizumab plus methotrexate: safety and efficacy over 106 weeks of treatment. Annals of the Rheumatic Diseases 2024;83:1454-1464. The correct figures 2 and 3 including descriptions provided on y-axis are below:
CD-19 CAR-T cells for polyrefractory rheumatoid arthritis
ML and DR are joint first authors. Handling editor Josef S Smolen X @doronrimar@gmail.com Contributors ML and DR contributed equally to this paper. ML, DR, PD, EJ, RSF, AS and AA conceived the idea and prepared the treatment protocol. ML, DR, PD, EJ and AA and wrote the letter. OI prepared the CAR-T cells. MDS and IE performed the radiological assessment of the patient. TS performed the pathological analysis of biopsy. GS, RM, RY, NST and ID completed patient assessments.
Pharmacodynamics of the S1P1 receptor modulator cenerimod in a phase 2b randomised clinical trial in patients with moderate to severe SLE
Systemic lupus erythematosus Pharmacodynamics of the S1P1 receptor modulator cenerimod in a phase 2b randomised clinical trial in patients with moderate to severe SLE Statistics from Altmetric.com Request Permissions If you wish to reuse any or all of this article please use the link below which will take you to the Copyright Clearance Center’s RightsLink service. You will be able to get a quick price and instant permission to reuse the content in many different ways.