Key result
Anti-TNF-α therapy linked to ~9-point increase in flow-mediated vasodilation in rheumatoid arthritis.
Cohort (n=28)
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Rheumatoid arthritis (RA) is associated with an excess cardiovascular morbidity and mortality, related to systemic inflammation with endothelial dysfunction (ED) and impaired flow-mediated vasodilation (FMD). We assessed the FMD response to anti-TNF-alpha treatments in 28 RA patients, aged 49.8+/-15.3 years: an unpaired FMD was found in 66.7 percent of our cases and was restored after 6 weeks of anti-TNF-á treatment (13.5+/-5.3 percent vs 4.6+/-4.1 percent, p less than 0.05). Twenty-five percent of the infliximab patients demonstrated a long term response, compared with 60 percent of etanercept and 100 percent of adalimumab patients, after 2 years (p less than 0.01). Infections (3 cases), myocardial ischemia (1 case) or loss of response (4 cases) were associated with a worsened FMD, restored by shifting to adalimumab. The present study confirms that ED is an RA systemic disease marker, responsive to anti-TNF-alpha treatment and sensitive to clinical events or to a loss of response, underlying the biological coherence between synovial and endothelial inflammation.
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Capria et al. (2010) conducted a cohort in Rheumatoid arthritis (n=28). Anti-TNF-α treatments vs. Baseline (pre-treatment) was evaluated on Flow-mediated vasodilation (FMD) (p=<0.05). Anti-TNF-α treatments significantly improved flow-mediated vasodilation in rheumatoid arthritis patients from 4.6% at baseline to 13.5% after 6 weeks (p<0.05).
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