Why the study?
Accelerated atherosclerosis and increased cardiovascular morbidity and mortality are associated with RA and AS, prompting assessment of anti-TNF therapy effects on vascular function.
Does anti-TNF-α therapy improve vascular function in patients with rheumatoid arthritis and ankylosing spondylitis?
Does anti-TNF-α therapy improve vascular function in patients with rheumatoid arthritis and ankylosing spondylitis?
Anti-TNF-α therapy over 12 months improves or stabilizes vascular pathophysiology, specifically flow-mediated vasodilation and pulse-wave velocity, in patients with rheumatoid arthritis and ankylosing spondylitis.
Answers are grounded in this paper and cite their sources.
May improve vascular function with anti-TNF in RA/AS; hypothesis-generating and leaves open CV outcome trials.
Accelerated atherosclerosis, increased cardiovascular morbidity and mortality have been associated with rheumatoid arthritis (RA) and ankylosing spondylitis (AS). Vascular function, clinical and laboratory markers and the effects of anti-TNF therapy were assessed in arthritides. Fifty-three 53 patients including 36 RA patients treated with either etanercept (ETN) or certolizumab pegol and 17 AS patients treated with ETN were included in a 12-month follow-up study. Ultrasonography was performed to determine flow-mediated vasodilation (FMD), common carotid intima-media thickness (ccIMT) and arterial pulse-wave velocity (PWV) in all patients. All assessments were performed at baseline and 6 and 12 months after treatment initiation. A significant improvement of brachial artery FMD was observed after 6 months (p = 0.004). A tendency of FMD improvement was also observed after 12 months (p = 0.065). ccIMT did not change throughout the year. PWV significantly improved after 12 months (p = 0.034). Higher baseline ccIMT (p = 0.009) and PWV (p = 0.038) were associated with clinical non-response (cNR) versus response (cR) to biologics. Multiple analysis confirmed the association of baseline ccIMT with age (p = 0.003) and cNR (p = 0.009), as well as that of baseline PWV with age at diagnosis (p = 0.022) and current chest pain (p = 0.004). Treatment itself determined the 12-month changes in FMD (p = 0.020) and PWV (p = 0.007). In a mixed cohort of RA and AS patients, TNF inhibition improved or stabilized vascular pathophysiology. Inflammation may be associated with FMD, while, among others, cNR may influence vascular function.
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Végh et al. (2019) studied this question.
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