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Abstract Number: 1374

Value of C-Reactive Protein Level At Diagnosis of Psoriatic Arthritis in Predicting the Future Need for Treatment with Tumor Necrosis Factor-á Inhibitors

Yair Molad1 and Shachaf Ofer-Shiber2, 1Rheumatology Unit, Beilinson Hospital, Rabin Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Petach-Tikva, Israel, 2Internal Medicine H, Beilinson Hospital, Rabin Medical Center and Sackler Faculty of Medicine, Tel Aviv University, Petah Tikva, Israel

Meeting: 2012 ACR/ARHP Annual Meeting

Keywords: anti-TNF therapy, C Reactive Protein, Disease-modifying antirheumatic drugs, psoriatic arthritis and treatment

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Session Information

Title: Spondylarthropathies and Psoriatic Arthritis: Clinical Aspects and Treatment

Session Type: Abstract Submissions (ACR)

Background/Purpose: To determine the value of acute-phase reactant levels at diagnosis of psoriatic arthritis in predicting the risk of failure of conventional treatment with disease-modifying anti-rheumatic drugs (DMARDs) and the consequent need for biologic treatment with a tumor necrosis factor (TNF) inhibitor.

Methods: Clinical, laboratory, and treatment data were collected from the medical files of a real-life inception cohort of 71 consecutive patients diagnosed with psoriatic arthritis (CASPAR criteria) in 2000-2011 at the rheumatology clinic of a tertiary medical center.  A logistic regression model was used to identify laboratory variables associated with TNF inhibitor use during the disease course.

Results: The cohort included 38 female (53.5%) and 33 male patients of mean age 41±10.4 years; 66 (93%) Jewish and 5 (7%) Arabic. Mean disease duration was 11.56±6.58 years. The most common clinical feature was symmetric polyarthritis (40.8%). All patients were treated with one or more DMARDs, mainly methotrexate (81.6%). Thirty-seven patients (52.11%) had an inadequate response and received at least one TNF inhibitor, at the discretion of the attending rheumatologist. C-reactive protein (CRP) level at diagnosis was positively correlated with need for a TNF inhibitor (p=0.009; hazard ratio = 1.8 95% CI 1.27-1.85). Patients with CRP >0.9 mg/dl at diagnosis started biologic treatment significantly earlier in the disease course than patients with a lower level (p=0.003, hazard ratio = 2.62 95% CI 0.393-2.5).

Conclusion: :  In patients with psoriatic arthritis, CRP ≥0.9mg/dl at diagnosis significantly predicts an inadequate response to conventional  DMARDs and the  probability that a TNF inhibitor will be needed to achieve disease control.


Disclosure:

Y. Molad,
None;

S. Ofer-Shiber,
None.

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