Autoantibodies and damage in patients with idiopathic inflammatory myopathies: A longitudinal multicenter study from the MYONET international network.
Fabricio Espinosa-OrtegaKarin LodinMaryam DastmalchiJiri VencovskyLouise P DiederichsenSamuel Katsuyuki ShinjoMaria Giovanna DanieliAlbert Selva-O'CallaghanMarianne de VisserZoltan GrigerAngela CeribelliDiana Gómez-MartinHelena AnderssonMónica Vázquez-Del MercadoHector ChinoyJames B LillekerPaul NewNiels S KroghIngrid E LundbergHelene Alexandersonnull nullPublished in: Seminars in arthritis and rheumatism (2024)
Our study is the first to describe patterns and trajectories of change in damage over time in relation to autoantibody defined subgroups in a large international multicenter cohort of patients with IIM. Patients with anti-PM/Scl scored a greater extent of damage, whereas patients with dermatomyositis-specific antibodies had less damage than seronegative patients. Severity in muscle damage had moderate to strong correlation with functional disability among the IMNM and seronegative subgroups with lower correlations for the other subgroups. These findings suggest that autoantibodies may be useful predictors of long-term damage.