Analyzing the risk of osteoporosis and fracture in rheumatoid arthritis patients who have been treated with various biologics

Abstract

BackgroundRheumatoid arthritis (RA) is a major risk factor for osteoporosis/osteoporotic fractures. We aimed to elucidate the role of treatment choices among osteoporosis/osteoporotic fractures.MethodologyWe utilized the Chang‐Gung Research Database to assess the risks of osteoporosis/osteoporotic fractures among independently treated RA patients, using retrospective time‐to‐event outcomes analysis.ResultsA total of 3509 RA patients with a mean of 63.1 ± 8.6 years were analyzed. Among all, 1300 RA patients (37%) were diagnosed with newly diagnosed osteoporosis. The crude incidence of newly diagnosed osteoporosis was the highest among those treated with other conventional disease‐modifying anti‐rheumatic drugs (cDMARDs; 74.1 events/1000‐PYs, 95%CI 66.0–82.3), followed by those with a non‐treatment period (68 events/1000‐PYs, 95%CI 63.1–72.9), methotrxate (MTX) monotherapy (60.7 events/1000‐PYs, 95%CI 41.2–80.3), MTX plus other cDMARDs (51.9 events/1000‐PYs, 95%CI 43.4–60.3), and abatacept/rituximab (48.6 events/1000‐PYs, 95%CI 14.9–82.3). The lowest crude incidence was found in patients treated with anti‐TNFi biologics (40.4 events/1000‐PYs, 95%CI 28.6–52.2) and other biologic disease‐modifying anti‐rheumatic drugs (bDMARDs; 40.1 events/1000‐PYs, 95%CI 8.0–72.1). A total of 270 patients (20.8%) suffered from an incident fracture during follow‐ups. The crude incidence of fracture was the highest among those treated with abatacept/rituximab (49.0 events/1000‐PYs, 95%CI 6.0–91.9), followed by those with non‐treatment periods (24.3 events/1000‐PYs, 95%CI 19.3–29.4), other cDMARDs (24.2 events/1000‐PYs, 95%CI 18.1–30.2), anti‐TNFi biologics (20.2 events/1000‐PYs, 95%CI 8.8–31.6). Other bDMARDs (13.3 events/1000‐PYs, 95%CI 0–39.2), MTX mono (12.5 events/1000‐PYs, 95%CI 0.3–24.8), and MTX plus other cDMARDs (11.4 events/1000‐PYs, 95%CI 5.4–17.4) were low incidences.ConclusionThe treatment option has emerged as a critical determinant in the context of future osteoporosis and osteoporotic fracture risks among RA. These findings offer a valuable resource for clinicians, empowering them to tailor bespoke treatment strategies for RA patients, thereby mitigating the potential for future osteoporosis and fractures.