Llorente Irene, Merino Leticia, Ortiz Ana M, Escolano Eugenio, González-Ortega Saturnino, García-Vicuña Rosario, García-Vadillo Jesús A, Castañeda Santos, González-Álvaro Isidoro
Rheumatology Department, Hospital Universitario de La Princesa, IIS-Princesa, C/ Diego de León 62, 28006, Madrid, Spain.
Rheumatology Department, Hospital San Pedro, Logroño, Spain.
Rheumatol Int. 2017 May;37(5):799-806. doi: 10.1007/s00296-017-3674-9. Epub 2017 Feb 27.
Since the previous studies showed that anti-citrullinated protein antibodies (ACPA) can induce osteoclasts differentiation and activation, even before arthritis onset, the aim of our study was to determine whether ACPA-positivity is associated with lower bone mineral density (BMD) at baseline visit of a register of early arthritis (EA) patients. The study population comprised 578 patients (80% females) from our EA clinic with a median disease duration, 5.1 months (p25-p75: 6-8); median age, 53.6 years (41.9-66.1), 38% ACPA-positive, and 55% fulfilling 2010 criteria for rheumatoid arthritis. BMD was measured using dual X-ray absorptiometry at lumbar spine, hip, and metacarpophalangeal (MCP) joints of the non-dominant hand to evaluate both systemic and juxta-articular bone mass. ACPA titers were determined through enzyme immunoassay. The effect of ACPA on BMD was analyzed using multivariable analysis based on generalized linear models adjusted for various confounders. ACPA-positive patients showed lower bone mass at lumbar spine and hip, but no differences were observed at MCP joints compared to ACPA-negative patients. However, ACPA-positive patients displayed higher disease activity and disability than ACPA-negative patients. After adjustment for gender, age, body mass index, and other bone-related variables, the presence of ACPA remained significantly associated with lower BMD at the lumbar spine, femoral neck, and hip but not at MCP joints. Disease activity was not associated with baseline bone mass. Our data reinforce the previous preclinical findings suggesting that the systemic bone loss detected at the initial phases of early ACPA-positive arthritis is independent of inflammatory status and, therefore, could be mediated by ACPA.
由于先前的研究表明,抗瓜氨酸化蛋白抗体(ACPA)甚至在关节炎发作之前就能诱导破骨细胞分化和激活,因此我们研究的目的是确定在早期关节炎(EA)患者登记册的基线访视时,ACPA阳性是否与较低的骨密度(BMD)相关。研究人群包括来自我们EA诊所的578名患者(80%为女性),疾病持续时间中位数为5.1个月(第25-75百分位数:6-8);年龄中位数为53.6岁(41.9-66.1),38%为ACPA阳性,55%符合2010年类风湿关节炎标准。使用双能X线吸收法在腰椎、髋部和非优势手的掌指(MCP)关节测量BMD,以评估全身和关节周围骨量。通过酶免疫测定法测定ACPA滴度。使用基于广义线性模型并针对各种混杂因素进行调整的多变量分析来分析ACPA对BMD的影响。与ACPA阴性患者相比,ACPA阳性患者在腰椎和髋部的骨量较低,但在MCP关节未观察到差异。然而,ACPA阳性患者比ACPA阴性患者表现出更高的疾病活动度和残疾程度。在调整性别、年龄、体重指数和其他与骨相关的变量后,ACPA的存在仍与腰椎、股骨颈和髋部的较低BMD显著相关,但在MCP关节则不然。疾病活动度与基线骨量无关。我们的数据强化了先前的临床前研究结果,表明在早期ACPA阳性关节炎的初始阶段检测到的全身骨质流失与炎症状态无关,因此可能由ACPA介导。