Reduction in the incidence of myocardial infarction in patients with rheumatoid arthritis who respond to anti-tumor necrosis factor α therapy -: Results from the British Society for Rheumatology Biologics Register

Objective. Rheumatoid arthritis (RA) is associated with an increased risk of coronary artery disease, possibly acting via shared mechanisms of inflammation. This study was undertaken to test the hypothesis that the powerful antiinflammatory effect of anti-tumor necrosis alpha (anti-TNF alpha) therapy might lead to a reduction in the incidence of myocardial infarction (MI) in patients with RA. Methods. Using data from the British Society for Rheumatology Biologics Register, a national prospective observational study, we compared MI rates in 8,670 patients with RA treated with anti-TNFa and 2,170 patients with active RA treated with traditional disease-modifying antirheumatic drugs (DMARDs). Results. Through July 2006, 63 MIs occurred in the anti-TNFa cohort during 13,233 person-years of followup and 17 MIs occurred in the DMARD cohort during 2,893 person-years of followup, equivalent to a rate of 4.8 events per 1,000 person-years and 5.9 events per 1,000 person-years, respectively. After adjustment for baseline risk factors, there was no reduction in the rate of MI in the anti-TNF alpha cohort compared with the DMARD cohort (incidence rate ratio 1.44 [95% confidence interval 0.56-3.67]). In an analysis of anti-TNF alpha-treated patients who responded to the treatment within 6 months versus those who did not, MI rates were found to be 3.5 events per 1,000 person-years in responders and 9.4 events per 1,000 person-years in nonresponders. The adjusted incidence rate ratio (95% confidence interval) for responders compared with nonresponders was 0.36 (0.19-0.69). Conclusion. These results indicate that RA patients treated with anti-TNFa do not have a lower incidence of MI compared with RA patients treated with traditional DMARDs. However, the risk of MI is markediy reduced in those who respond to anti-TNFa therapy by 6 months compared with nonresponders. This finding supports the notion that inflammation plays a pivotal role in MI.