Takeaway
- Various autoimmune diseases targeting different organs were associated with an increased risk of new-onset atrial fibrillation (AF), especially in women.
Why This Matters
- Findings expand on and add to our understanding of the pathophysiological differences in autoimmunity between men and women.
Study Design
- An analysis of 494,072 participants without AF (men, n=223,268; women, n=270,804) identified using data from the UK Biobank.
- Funding: Erasmus Medical Centre grant and the Senior Scientist Grant from the Dutch Heart Foundation.
Key Results
- After a median follow-up of 12.8 years, 16,804 (7.5%) men and 10,390 (3.8%) women developed new-onset AF.
- The risk of new-onset AF was higher with (adjusted HR [aHR]; 95% CI):
- rheumatic fever without heart involvement (1.47; 1.26 to 1.72);
- Crohn’s disease (1.23; 1.05 to 1.45);
- ulcerative colitis (1.17; 1.05 to 1.31);
- rheumatoid arthritis (1.39; 1.28 to 1.51);
- polyarteritis nodosa (1.79; 1.04 to 3.09);
- systemic lupus erythematosus (1.82; 1.41 to 2.35); and
- systemic sclerosis (2.32; 1.57 to 3.44).
- In women, the risk of new-onset AF was higher with (aHR; 95% CI):
- rheumatic fever without heart involvement (1.79; 1.45 to 2.20);
- Crohn’s disease (1.35; 1.05 to 1.73);
- musculoskeletal and connective tissue disorders (1.51; 1.38 to 1.66);
- rheumatoid arthritis (1.50; 1.35 to 1.67);
- psoriatic and enteropathic arthropathies (2.01; 1.32 to 3.05);
- systemic lupus erythematosus (1.79; 1.34 to 2.40);
- systemic sclerosis (2.51; 1.64 to 3.85); and
- ankylosing spondylitis (1.53; 1.13 to 2.07).
Limitations
- Some of the autoimmune diseases of interest were low in prevalence because of the rarity of diseases.
References
References