Abstract
Background The link between rheumatoid arthritis (RA) and atrial fibrillation (AF) has received less attention. Objective This study aimed to examine the association between RA and incident AF in a nationwide cohort, with particular focus on differences according to serostatus - seropositive RA (SPRA) and seronegative RA (SNRA). We explored the potential influence of biologic or targeted synthetic disease-modifying antirheumatic drugs (b/tsDMARDs) use as a secondary objective. Methods This retrospective cohort study used the National Health Insurance Service database to include participants who were first diagnosed with RA between 2010 and 2017. Matched non-RA controls were selected by age and sex (1:3 ratio). Participants were followed from 1 year after the index date (to mitigate surveillance bias) until December 31, 2020. Results A total of 48,885 patients with RA (34,699 SPRA, 14,186 SNRA) and 146,655 matched controls were included. Patients with RA had a significantly higher risk of AF than non-RA controls (adjusted hazard ratio [aHR] 1.55, 95% confidence interval 1.46-1.65). Both patients with SPRA and SNRA had a higher AF risk than non-RA controls (aHR 1.63 in SPRA, 1.37 in SNRA). Patients with SPRA had a higher risk compared with those with SNRA (aHR 1.19, 95% confidence interval 1.02-6.34). The use of biologic disease-modifying antirheumatic drugs was associated with a slightly higher risk of AF, while targeted synthetic disease-modifying antirheumatic drug use led to risk reduction, but was not statistically significant. Conclusion This study shows that both patients with SPRA and SNRA are at a significantly greater risk for AF compared with non-RA controls, with patients with SPRA at the highest risk.
| Original language | English |
|---|---|
| Pages (from-to) | 525-533 |
| Number of pages | 9 |
| Journal | Heart Rhythm |
| Volume | 23 |
| Issue number | 3 |
| DOIs | |
| State | Published - 1 Mar 2026 |
Keywords
- Atrial fibrillation
- DMARDs
- Rheumatoid arthritis
- Seronegative
- Seropositive
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