Methotrexate and anti-tumor necrosis factor treatment improves endothelial function in patients with inflammatory arthritis

Inflammatory arthritis (IA), including rheumatoid arthritis (RA), ankylosing spondylitis (AS) and psoriatic arthritis (PsA), leads to increased cardiovascular disease occurrence probably due to atherosclerosis. One of the first stages in atherogenesis is endothelial dysfunction (ED). Therefore, we a...

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Veröffentlicht in:Arthritis research & therapy 2017-10, Vol.19 (1), p.232-232, Article 232
Hauptverfasser: Deyab, Gia, Hokstad, Ingrid, Whist, Jon Elling, Smastuen, Milada Cvancarova, Agewall, Stefan, Lyberg, Torstein, Ronda, Nicoletta, Mikkelsen, Knut, Hjeltnes, Gunnbjorg, Hollan, Ivana
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Sprache:eng
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Zusammenfassung:Inflammatory arthritis (IA), including rheumatoid arthritis (RA), ankylosing spondylitis (AS) and psoriatic arthritis (PsA), leads to increased cardiovascular disease occurrence probably due to atherosclerosis. One of the first stages in atherogenesis is endothelial dysfunction (ED). Therefore, we aimed to compare endothelial function (EF) in patients with IA, and to examine the effects of methotrexate (MTX) monotherapy and antitumor necrosis factor (anti-TNF) treatment with or without MTX comedication (anti-TNF ± MTX) on EF. From the PSARA observational study, all patients with RA (n = 64), PsA (n = 29), and AS (n = 20) were evaluated for EF. In patients with ED at baseline (n = 40), we evaluated changes in the Reactive Hyperemic Index (RHI) after 6 weeks and 6 months of antirheumatic therapy. In IA patients with ED, RHI significantly improved after 6 weeks (p 
ISSN:1478-6362
1478-6354
1478-6362
DOI:10.1186/s13075-017-1439-1