Back to Search Start Over

Clinical Characteristics of Anti-synthetase Syndrome: Analysis From the Classification Criteria for Anti-Synthetase Syndrome Project.

Authors :
Faghihi-Kashani S
Yoshida A
Bozan F
Zanframundo G
Rozza D
Loganathan A
Dourado E
Sambataro G
Bauer-Ventura I
Bae SS
Lim D
Rivero-Gallegos D
Yamano Y
Selva-O'Callaghan A
Mammen AL
Scirè CA
Montecucco C
Oddis CV
Fiorentino D
Bonella F
Miller FW
Lundberg IE
Schmidt J
Rojas-Serrano J
Hudson M
Kuwana M
González-Gay MA
McHugh N
Corte TJ
Doyle TJ
Werth VP
Gupta L
Perez Roman DI
Bianchessi LM
Devarasetti PK
Shinjo SK
Luppi F
Cavazzana I
Moghadam-Kia S
Fornaro M
Volkmann ER
Piga M
Loarce-Martos J
De Luca G
Knitza J
Wolff-Cecchi V
Sebastiani M
Schiffenbauer A
Rider LG
Campanilho-Marques R
Marts L
Bravi E
Gunawardena H
Aggarwal R
Cavagna L
Source :
Arthritis & rheumatology (Hoboken, N.J.) [Arthritis Rheumatol] 2024 Oct 28. Date of Electronic Publication: 2024 Oct 28.
Publication Year :
2024
Publisher :
Ahead of Print

Abstract

Objective: Anti-synthetase syndrome (ASSD) is a rare systemic autoimmune rheumatic disease (SARD) with significant heterogeneity and no shared classification criteria. We aimed to identify clinical and serological features associated with ASSD that may be suitable for inclusion in the data-driven classification criteria for ASSD.<br />Methods: We used a large, international, multicenter "Classification Criteria for Anti-synthetase Syndrome" (CLASS) project database, which includes both patients with ASSD and controls with mimicking conditions, namely, SARDs and/or interstitial lung disease (ILD). The local diagnoses of ASSD and controls were confirmed by project team members. We employed univariable logistic regression and multivariable Ridge regression to evaluate clinical and serological features associated with an ASSD diagnosis in a randomly selected subset of the cohort.<br />Results: Our analysis included 948 patients with ASSD and 1,077 controls. Joint, muscle, lung, skin, and cardiac involvement were more prevalent in patients with ASSD than in controls. Specific variables associated with ASSD included arthritis, diffuse myalgia, muscle weakness, muscle enzyme elevation, ILD, mechanic's hands, secondary pulmonary hypertension due to ILD, Raynaud phenomenon, and unexplained fever. In terms of serological variables, Jo-1 and non-Jo-1 anti-synthetase autoantibodies, antinuclear antibodies with cytoplasmic pattern, and anti-Ro52 autoantibodies were associated with ASSD. In contrast, isolated arthralgia, dysphagia, electromyography/magnetic resonance imaging/muscle biopsy findings suggestive of myopathy, inflammatory rashes, myocarditis, and pulmonary arterial hypertension did not differentiate between patients with ASSD and controls or were inversely associated with ASSD.<br />Conclusion: We identified key clinical and serological variables associated with ASSD, which will help clinicians and offer insights into the development of data-driven classification criteria for ASSD.<br /> (© 2024 The Author(s). Arthritis & Rheumatology published by Wiley Periodicals LLC on behalf of American College of Rheumatology. This article has been contributed to by U.S. Government employees and their work is in the public domain in the USA.)

Details

Language :
English
ISSN :
2326-5205
Database :
MEDLINE
Journal :
Arthritis & rheumatology (Hoboken, N.J.)
Publication Type :
Academic Journal
Accession number :
39467037
Full Text :
https://doi.org/10.1002/art.43038