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SAT0049 Serum Concentrations of OPG and Rankl in Rheumatoid Arthritis in Different Biologic Therapies
  1. K. Romanowska-Prόchnicka1,2,
  2. A. Paradowska-Gorycka3,
  3. M. Olesińska4,
  4. M. Mańczak5,
  5. A. Felis-Giemza4,
  6. D. Szukiewicz4,
  7. S. Maśliński6
  1. 1Department of General and Experimental Pathology, Warsaw Medical University
  2. 2Department and Polyclinic of Systemic Connective Tissue Diseases, Institute of Rheumatology, Warszawa
  3. 3Department of Biochemistry and Molecular Biology
  4. 4Department and Polyclinic of Systemic Connective Tissue Diseases
  5. 5Department of Epidemiology and Health Promotion, Institute of Rheumatology
  6. 6Department of General and Experimental Pathology, Warsaw Medical University, Warsaw, Poland

Abstract

Background Osteoprotegerin (OPG) is a soluble decoy receptor which blocks osteoclast differentiation and activation by neutralizing the receptor activator of NF-κB ligand (RANKL). The balance between RANKL, which stimulates osteoclastogenesis and osteoclastic activation, and its physiological antagonist OPG plays a critical role in the regulation of bone resorption in rheumatoid arthritis (RA).

Objectives The aim of the study was to examine the impact of various drug therapies in RA on the bone turnover activity markers, i.e. sRANKL and OPG.

Methods A group of 125 patients (pts) with RA and a control group of 42 healthy people have been qualified to the study. All patients fulfilled the American College of Rheumatology (ACR 2010) criteria for RA. RA group was divided into several subgroups. First group included 39 RA pts on Leflunomide. Second group included 49 RA pts on Methotrexate (MTX) and etanercept (First line biologic therapy). Third group included 16 RA pts on MTX and adalibumab, golibumab, infliksimab. (Second line biologic therapy). Fourth group included 16 RA pts on MTX and antiCD20 or anti IL6 (Third line biologic therapy). Fifth group included 44 RA pts on Disease-modifying antirheumatic drugs (DMARD's), 39 of them were included into Leflunomide therapy, also with intolerable toxicity to MTX. Estimated research period was 12 months. Average age of participants was 54 (22-79 years). All pts have been examined based on DAS28 before and after 90 days of therapy. The blood samples for bone markers RANKL and OPG levels were measured by ELISA after 90 days therapy. Bone erosions in hands and feet were evaluated by Larsen methods. Dexa scan of femoral neck was performed.

Results All subgroups of RA pts were compared in respect of markers of osteoporosis. The individual groups of pts do not differ from each other in the following parameters: the radiological destructions of the disease, organ damage, presence of anti-CCP and RF, the average use of GKS, and co-occurrence with osteoporosis and osteopenia. The above-mentioned groups of pts were relatively homogeneous.

In all groups of RA pts treated with various therapies decreased level of sRANKL/OPG has been observed compared to DMARD therapy (Leflunomide to DMARD's- p-0,06, First line biologic therapy to DMARD's- p-0,05, Second line biologic therapy to DMARD's- p-0,04, Third line biologic therapy to DMARD's p-0,001. Additionally in the RA group treated with anti CD20 and anti IL6 therapy serum OPG level was significantly higher than in other group (p-0,003). Furthermore, serum sRANKL level was reduced in the third-line therapy compared to DMARD's (p-0,003).

Conclusions In conclusion, our findings indicate that both OPG as well as sRANKL help with evaluation of treatment effectiveness in RA and are useful parameters in daily clinical practice.

Disclosure of Interest None declared

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