Abstract
than the general population. Rheumatoid arthritis (RA) is a chronic inflammatory rheumatic disease and a frequent cause of secondary osteoporosis induced by the chronic inflammatory condition and a long-term glucocorticoid therapy (GC). The aim of this study is to evaluate the influence of GC on the trabecular bone score (TBS), BMD and TBS dynamics during one year in patients with RA. Methods: 134 examined women with RA (age 52.5 12.8 years; height 162.6 6.4 cm, weight 68.2 13.7 kg, duration of disease 9.1 7.5 years, duration of postmenopausal period 7.6 7.2 years) were divided into three groups: first group, G1e37 patients who did not use GC; second group, G2e 50 patients who used GC in a dose of O5 mg of prednisolone for more than 3 years; third group, G3 e 47 patients who took GC only at the exacerbated stage for!6 months. All the patients had been takingmethotrexate as a basic treatment. BMD of total body, PA lumbar spine, proximal femur and forearm were measured using the DXA method (Prodigy, GEHC Lunar, Madison,WI, USA) and PA spine TBSwas assessed bymeans of TBS iNsight software package installed on our DXA machine (Med-Imaps, Pessac, France). Evaluation of TBS dynamics in the patients of G1 and G2 groups during the year was conducted on the background of ongoing therapy which included doses of GC (for the patients of second group) and/or without any osteotropic treatment. Results: The 3 groups did not differ as to age, basic anthropometric parameters, duration of disease and duration of postmenopausal period in these groups. TBS in G2 was significantly lower compared to G1 (TBSL1-L4: 1.147 0.168 vs. 1.250 0.135; t5-3.07; p50.003), and G3 compared to G1 (TBS L1-L4: 1.274 0.138; t53.95; p50.0002). However, there were no differences in BMD of PA spine and hip among groups. Only forearm BMD in the second group was significantly lower compared to the first one (0.583 0.176 g/cm vs. 0.675 0.229 g/cm; t5-2.18; p50.032). Spine TBS decreased by 1.4% after one year for G1 and by 5.8% for G2. Conclusion: For patients who are GC users, TBS, but not BMD, reflects bone microarchitecture deterioration which is an indicator for those patients to of a higher vertebrae and nonvertebral risk of fracture. TBS is a determinant of bone state and must be monitored during the long-term treatment with GC. Disclosure of Interest: None Declared
Published Version
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