Observational study shows cumulative incidence of remission and diagnosis change in individuals with seronegative RA, highlighting treatment implications.
Objective The purpose of this study was to determine the cumulative incidence of diagnosis switching, drug‐free remission, and initiation of a biologic or targeted synthetic disease modifying anti‐rheumatic drug (b/tsDMARD) in individuals with seronegative RA. Methods Adult residents of Olmsted County, MN with incident seronegative (rheumatoid factor‐/anti‐cyclic citrullinated peptide antibody‐) RA meeting the 1987 and/or 2010 American College of Rheumatology classification criteria were included. Data were collected from 1/1/2005‐12/31/2023 through manual chart review. Drug‐free remission was defined as a period of ≥6 months where the individual was no longer on treatment for RA and did not have evidence of active inflammatory arthritis on evaluation by a rheumatologist. We calculated the 10‐year cumulative incidence of a change in diagnosis, adjusting for the competing risk of death, and of drug‐free remission and initiation of a b/tsDMARD, adjusting for the competing risks of death or change in diagnosis. Results A total of 176 individuals with seronegative RA (68% female) were included. The 10‐year cumulative incidence of a change in diagnosis was 12.8% (95% confidence interval (CI): 8.7‐18.9%). The most common change in diagnosis was to a spondyloarthritis (4%). The 10‐year cumulative incidence of drug‐free remission and initiation of a b/tsDMARD was 26.6% (95% CI: 20.7‐34.2%) and 19.9% (95% CI: 14.7‐26.9%), respectively. Over a median follow‐up of 11.8 years, 49 individuals entered drug‐free remission. Conclusions After initial diagnosis of seronegative RA, about 13% of individuals had a change in diagnosis and a quarter experienced drug‐free remission within 10 years.
No takes yet. Share an insight, caveat, or question.
Kimbrough et al. (2025) studied this question.
Synapse has enriched 5 closely related papers on similar clinical questions. Consider them for comparative context: