Jarrett Stephen J, Conaghan Philip G, Sloan Victor S, Papanastasiou Philemon, Ortmann Christine-Elke, O'Connor Philip J, Grainger Andrew J, Emery Paul
University of Leeds, Leeds, UK.
Arthritis Rheum. 2006 May;54(5):1410-4. doi: 10.1002/art.21824.
Bisphosphonates inhibit osteoclast activity, which is central to the development of bone damage in rheumatoid arthritis (RA). The aim of this study was to assess whether treatment with zoledronic acid, compared with placebo, could achieve a > or = 50% reduction in the development of new erosions on magnetic resonance imaging (MRI) in patients with early RA.
In this proof-of-concept study, 39 patients with early RA and clinical synovitis of the hand/wrist were randomized to receive infusions with either zoledronic acid (5 mg) or placebo, administered at baseline and week 13. Patients in both groups received methotrexate (MTX) at a dosage of 7.5-20 mg/week. MRI and plain radiography were performed at baseline and week 26.
At week 26, the mean +/- SD change in MRI hand and wrist erosions was 61% lower in the zoledronic acid group compared with the placebo group (0.9 +/- 1.63 versus 2.3 +/- 3.09; P = 0.176). The mean +/- SD increase in the number of hand and wrist bones with erosions was 0.3 +/- 0.75 for zoledronic acid compared with 1.4 +/- 1.77 for placebo (P = 0.029). The proportion of patients in whom new MRI-visualized bone edema developed was smaller in the zoledronic acid group compared with the placebo group (33% versus 58%; P = 0.121). The zoledronic acid group had a mean change in the number of radiographic erosions of 0.1 compared with 0.5 for the placebo group (P = 0.677). The safety profile of zoledronic acid was similar to that of placebo.
The results of this study suggest a structural benefit associated with zoledronic acid therapy in patients with RA, as demonstrated by consistent results in structural end points in favor of zoledronic acid plus MTX compared with MTX alone.
双膦酸盐可抑制破骨细胞活性,而破骨细胞活性是类风湿关节炎(RA)骨损伤发展的关键因素。本研究旨在评估与安慰剂相比,唑来膦酸治疗能否使早期RA患者磁共振成像(MRI)上新出现侵蚀灶的进展减少≥50%。
在这项概念验证研究中,39例患有早期RA且手部/腕部有临床滑膜炎的患者被随机分为接受唑来膦酸(5mg)或安慰剂静脉输注,分别在基线期和第13周给药。两组患者均接受剂量为7.5 - 20mg/周的甲氨蝶呤(MTX)治疗。在基线期和第26周进行MRI和X线平片检查。
在第26周时,与安慰剂组相比,唑来膦酸组手部和腕部MRI侵蚀灶的平均变化(均值±标准差)降低了61%(0.9±1.63对2.3±3.09;P = 0.176)。唑来膦酸组手部和腕部出现侵蚀的骨骼数量的平均增加(均值±标准差)为0.3±0.75,而安慰剂组为1.4±1.77(P = 0.029)。与安慰剂组相比,唑来膦酸组中出现新的MRI可见骨水肿的患者比例更小(33%对58%;P = 0.121)。唑来膦酸组X线侵蚀灶数量的平均变化为0.1,而安慰剂组为0.5(P = 0.677)。唑来膦酸的安全性与安慰剂相似。
本研究结果表明,唑来膦酸治疗对RA患者有结构方面的益处,与单独使用MTX相比,唑来膦酸联合MTX在结构终点方面的一致结果证明了这一点。