Effects of 1-year anti-TNF-α therapy on vascular function in rheumatoid arthritis and ankylosing spondylitis

被引:0
作者
Edit Végh
György Kerekes
Anita Pusztai
Attila Hamar
Szilvia Szamosi
Andrea Váncsa
Levente Bodoki
Lilla Pogácsás
Fruzsina Balázs
Katalin Hodosi
Andrea Domján
Sándor Szántó
Zoltán Nagy
Zoltán Szekanecz
Gabriella Szűcs
机构
[1] University of Debrecen,Department of Rheumatology, Institute of Medicine
[2] Faculty of Medicine,Department of Angiology, Institute of Medicine
[3] University of Debrecen,Department of Sports Medicine
[4] Faculty of Medicine,undefined
[5] University of Debrecen,undefined
[6] Faculty of Medicine,undefined
来源
Rheumatology International | 2020年 / 40卷
关键词
Rheumatoid arthritis; Ankylosing spondylitis; Atherosclerosis; Cardiovascular disease; Flow-mediated vasodilation; Pulse-wave velocity; Carotid intima-media thickness;
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摘要
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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页码:427 / 436
页数:9
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