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Changes in arterial stiffness during continued infliximab treatment in patients with inflammatory arthropathies
Authors:Kristin Angel  Sella Aarrestad Provan  Hilde Berner Hammer  Petter Mowinckel  Tore Kristian Kvien  Dan Atar
Affiliation:1. Division of Cardiology, Oslo University Hospital Aker, 0514 Oslo, Norway;2. Department of Rheumatology, Diakonhjemmet Hospital, PB 23 Vinderen, 0319 Oslo, Norway;3. Faculty of Medicine, University of Oslo, PB 1078 Blinderen, 0316 Oslo, Norway
Abstract:Chronic inflammatory arthropathies such as rheumatoid arthritis (RA), ankylosing spondylitis (AS), and psoriatic arthritis (PsA) are associated with an increased risk of cardiovascular disease. TNF‐α antagonists may improve vascular function in these patients and thus be beneficial with regard to cardiovascular disease. This study evaluated arterial stiffness and disease activity between two infusions with a TNF‐α antagonist (infliximab) in patients with inflammatory arthropathies on long‐term infliximab therapy. Augmentation index (AIx), aortic pulse wave velocity (aPWV), and disease activity were measured in 17 patients with RA, AS, or PsA who had been treated with infliximab for at least 12 months. The patients were examined immediately before their infliximab infusion and thereafter every 10th day until their next infusion scheduled at week 4–8. AIx and aPWV did not change during the period between two infliximab infusions. The patients had a temporary improvement in the general disease activity assessed on visual analogue scales by the patients (P = 0.04) and the investigator (P = 0.02) after the infusion. In the group of patients with RA, the Disease Activity Score (DAS28) changed significantly in a similar manner (P = 0.003). C‐reactive protein and erythrocyte sedimentation rate remained unchanged. Infliximab infusions did not alter aortic pulse wave velocity or augmentation index in patients with inflammatory arthropathies who were on long‐term infliximab therapy. Reductions in the general disease activity and DAS28 were not reflected in alterations of aortic stiffness or augmentation index.
Keywords:arterial stiffness  arthritis rheumatoid  atherosclerosis  inflammation  vasculature
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