首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Effects of etanercept versus sulfasalazine in early axial spondyloarthritis on active inflammatory lesions as detected by whole-body MRI (ESTHER): a 48-week randomised controlled trial.
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Effects of etanercept versus sulfasalazine in early axial spondyloarthritis on active inflammatory lesions as detected by whole-body MRI (ESTHER): a 48-week randomised controlled trial.

机译:通过全身MRI(ESTHER)检测,依那西普与柳氮磺胺吡啶在早期轴向性脊柱关节炎中对活动性炎性病变的影响:一项48周的随机对照试验。

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PURPOSE: To evaluate the potential of etanercept versus sulfasalazine to reduce active inflammatory lesions on whole-body MRI in active axial spondyloarthritis with a symptom duration of less than 5 years. METHODS: Patients were randomly assigned to etanercept (n=40) or sulfasalazine (n=36) treatment over 48 weeks. All patients showed active inflammatory lesions (bone marrow oedema) on MRI in either the sacroiliac joints or the spine. MRI was performed at weeks 0, 24 and 48 and was scored for active inflammatory lesions in sacroiliac joints and the spine including posterior segments and peripheral enthesitis by two radiologists, blinded for treatment arm and MRI time point. RESULTS: In the etanercept group, the reduction of the sacroiliac joint score from 7.7 at baseline to 2.0 at week 48 was significantly (p=0.02) larger compared with the sulfasalazine group from 5.4 at baseline to 3.5 at week 48. A similar difference in the reduction of inflammation was found in the spine from 2.2 to 1.0 in the etanercept group versus from 1.4 to 1.3 in the sulfasalazine group between baseline and week 48, respectively (p=0.01). The number of enthesitic sites also improved significantly from 26 to 11 in the etanercept group versus 24 to 26 in the sulfasalazine group (p=0.04 for difference). 50% of patients reached clinical remission in the etanercept group versus 19% in the sulfasalazine group at week 48. CONCLUSION: In patients with early axial spondyloarthritis active inflammatory lesions detected by whole-body MRI improved significantly more in etanercept versus sulfasalazine-treated patients. This effect correlated with a good clinical response in the etanercept group.
机译:目的:评价依那西普与柳氮磺胺吡啶在症状持续时间少于5年的活动性轴向脊柱关节炎中通过全身MRI减少活动性炎症损伤的潜力。方法:患者在48周内被随机分配接受依那西普(n = 40)或柳氮磺胺吡啶(n = 36)治疗。所有患者的sa关节或脊柱MRI均显示出活动性炎性病变(骨髓水肿)。 MRI分别在第0、24和48周进行,并由两名放射科医师对sa关节和脊柱(包括后段和周围性皮炎)的活动性炎性病变进行评分,但对治疗臂和MRI时间点视而不见。结果:在依那西普组中,sa关节评分从基线时的7.7降低到第48周的2.0显着(p = 0.02),而柳氮磺胺吡啶组从基线时的5.4降低到第48周的3.5。在基线和第48周之间,依那西普组的脊柱发炎率从2.2降低到1.0,而柳氮磺胺吡啶组的发炎率从1.4降低到1.3(p = 0.01)。依那西普组的麻醉位点数量也从26处显着改善到11处,而柳氮磺胺吡啶组的24处显着改善(差异p = 0.04)。在第48周时,依那西普组50%的患者达到临床缓解,而柳氮磺胺吡啶组为19%。结论:依那西普治疗的早期轴性脊柱关节炎患者通过全身MRI检测发现,活动性炎性病变比经柳氮磺胺吡啶治疗的患者明显改善。该作用与依那西普组良好的临床反应相关。

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