Charité Universitätsmedizin Berlin, Campus Benjamin Franklin, Berlin, Germany.
German Rheumatism Research Centre, Berlin, Germany.
Arthritis Rheumatol. 2016 Aug;68(8):1899-903. doi: 10.1002/art.39690.
To investigate the course of active inflammatory and fatty lesions seen on magnetic resonance imaging (MRI) in patients with early axial spondyloarthritis (SpA) treated with the tumor necrosis factor (TNF) inhibitor infliximab added to naproxen as compared to those treated with naproxen alone.
A total of 158 patients with active axial SpA were randomized (2:1) to receive 28 weeks of treatment with either infliximab 5 mg/kg plus naproxen 1,000 mg/day or placebo plus naproxen 1,000 mg/day. MRI of the sacroiliac (SI) joints and of the spine was performed at baseline and week 28. Images were scored for active inflammation and for fatty lesions.
After 28 weeks, there was a significant reduction of inflammation in the spine and in the SI joints in both treatment groups, which was, however, more prominent in the infliximab plus naproxen group (mean ± SD spine osteitis change score -2.9 ± 5.1, versus -2.0 ± 4.2 in the placebo plus naproxen group [P < 0.001]; SI joint osteitis change score -4.3 ± 5.2 in the infliximab plus naproxen group versus -3.9 ± 3.7 in the placebo plus naproxen group [P = 0.003]). Similarly, there was a significant increase in the fatty lesion score after 28 weeks in both groups; this change did not, however, differ significantly between groups (spine fatty lesion change score 0.8 ± 1.7 in the infliximab plus naproxen group versus 1.0 ± 1.8 in the placebo plus naproxen group [P = 0.72]; SI joint fatty lesion change score 1.7 ± 2.7 in the infliximab plus naproxen group versus 1.4 ± 2.6 in the placebo plus naproxen group [P = 0.86]).
These findings indicate that effective antiinflammatory treatment of axial SpA is associated with an increase in fatty lesion scores, independent of concomitant treatment with or without anti-TNF.
研究肿瘤坏死因子(TNF)抑制剂英夫利昔单抗联合萘普生与单独使用萘普生治疗早期轴性脊柱关节炎(SpA)患者的磁共振成像(MRI)上活跃性炎症和脂肪病变的进程。
共 158 例活动性轴性 SpA 患者被随机(2:1)分配至接受 28 周英夫利昔单抗 5mg/kg 联合萘普生 1000mg/天或安慰剂联合萘普生 1000mg/天治疗。基线和 28 周时对骶髂(SI)关节和脊柱行 MRI 检查。图像对活跃性炎症和脂肪病变进行评分。
28 周后,两组脊柱和 SI 关节的炎症均显著减轻,但英夫利昔单抗联合萘普生组减轻更显著(脊柱骨炎变化评分平均 ± 标准差-2.9 ± 5.1,安慰剂联合萘普生组为-2.0 ± 4.2 [P < 0.001];SI 关节骨炎变化评分-4.3 ± 5.2 英夫利昔单抗联合萘普生组,安慰剂联合萘普生组为-3.9 ± 3.7 [P = 0.003])。同样,两组在 28 周时脂肪病变评分也均显著增加,但组间无显著差异(脊柱脂肪病变变化评分英夫利昔单抗联合萘普生组为 0.8 ± 1.7,安慰剂联合萘普生组为 1.0 ± 1.8 [P = 0.72];SI 关节脂肪病变变化评分英夫利昔单抗联合萘普生组为 1.7 ± 2.7,安慰剂联合萘普生组为 1.4 ± 2.6 [P = 0.86])。
这些发现表明,有效的抗 SpA 炎症治疗与脂肪病变评分的增加相关,而与是否联合使用抗 TNF 无关。