The authors are the principal investigators of the British Society of Rheumatology (BSR) Biologics Register. The BSR receives financial support for the Register from the manufacturers of biologic agents currently licensed for use in the treatment of patients with inflammatory rheumatic diseases. The
Pharmacokinetic modeling of dynamic contrast-enhanced MRI of the hand and wrist in rheumatoid arthritis and the response to anti-tumor necrosis factor-α therapy
✍ Scribed by Richard J. Hodgson; Sylvia Connolly; Theresa Barnes; Brian Eyes; Robert S.D. Campbell; Robert Moots
- Publisher
- John Wiley and Sons
- Year
- 2007
- Tongue
- English
- Weight
- 355 KB
- Volume
- 58
- Category
- Article
- ISSN
- 0740-3194
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✦ Synopsis
Abstract
Dynamic contrast‐enhanced MRI (DCE‐MRI) of the hand and wrist was performed in 11 patients with rheumatoid arthritis twice before and once 2 weeks after treatment with anti–tumor necrosis factor (TNF)‐α therapy. A rapid, T~1~‐weighted 3D spoiled gradient echo (SPGR) sequence was used for the dynamic imaging. T~1~ estimation was performed using similar images obtained at different flip angles. The relative radiofrequency field was estimated from the known T~1~ of the periarticular fatty marrow. The arterial input function (AIF) was measured at each examination, and normalized to the expected plasma concentration to reduce partial volume effects. Synovial enhancement was modeled to yield values for K^trans^, v~e~, and v~p~. K^trans^ and v~e~ showed good reproducibility. There was a significant decrease of about 20% in K^trans^ after 2 weeks of treatment. This study demonstrates the potential of DCE‐MRI and pharmacokinetic modeling to study early changes in inflammatory activity in rheumatoid arthritis following treatment. Magn Reson Med 58:482–489, 2007. © 2007 Wiley‐Liss, Inc.
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## Abstract ## Objective To assess the association between the initiation of anti–tumor necrosis factor α (anti‐TNFα) therapy and the risk of serious bacterial infections in routine care. ## Methods This was a cohort study of patients with rheumatoid arthritis (RA) in whom specific disease‐modif