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首页> 外文期刊>BioMed research international >Predictive Factors of Clinical Response of Infliximab Therapy in Active Nonradiographic Axial Spondyloarthritis Patients
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Predictive Factors of Clinical Response of Infliximab Therapy in Active Nonradiographic Axial Spondyloarthritis Patients

机译:活增生术治疗活性无肌瘤轴向脊椎关节炎患者临床响应的预测因素

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Objectives. To evaluate the efficiency and the predictive factors of clinical response of infliximab in active nonradiographic axial spondyloarthritis patients. Methods. Active nonradiographic patients fulfilling ESSG criteria for SpA but not fulfilling modified New York criteria were included. All patients received infliximab treatment for 24 weeks. The primary endpoint was ASAS20 response at weeks 12 and 24. The abilities of baseline parameters and response at week 2 to predict ASAS20 response at weeks 12 and 24 were assessed using ROC curve and logistic regression analysis, respectively. Results. Of 70 axial SpA patients included, the proportions of patients achieving an ASAS20 response at weeks 2, 6,12, and 24 were 85.7%, 88.6%, 87.1%, and 84.3%, respectively. Baseline MRI sacroiliitis score (AUC = 0.791; P = 0.005), CRP (AUC = 0.75; P = 0.017), and ASDAS (AUC = 0.778, P = 0.007) significantly predicted ASAS20 response at week 12. However, only ASDAS (AUC = 0.696, P = 0.040) significantly predicted ASAS20 response at week 24. Achievement of ASAS20 response after the first infliximab infusion was a significant predictor of subsequent ASAS20 response at weeks 12 and 24 (wald X~2 = 6.87,P = 0.009, and wald X~2 = 5.171, P = 0.023). Conclusions. Infliximab shows efficiency in active nonradiographic axial spondyloarthritis patients. ASDAS score and first-dose response could help predicting clinical efficacy of infliximab therapy in these patients.
机译:目标。评价英夫利昔单抗临床响应效率和预测因素在活性非显影轴向脊柱型患者中的临床反应。方法。包括符合SPA的ESSG标准但未满足修改修改的纽约标准的活跃的非显影患者。所有患者均接受了英夫利昔单抗治疗24周。主要终点在第12周和24周内是ASAS20响应。使用ROC曲线和逻辑回归分析评估基线参数和第2周第2周和24周内响应的响应的能力。结果。在包括70例轴向SPA患者中,在第2周,6,12和24周内实现ASAS20响应的患者的比例分别为85.7%,88.6%,87.1%和84.3%。基线MRI骶髂炎得分(AUC = 0.791; P = 0.005),CRP(AUC = 0.75; P = 0.017),ASDAS(AUC = 0.778,P = 0.007)在第12周明显预测ASAS20响应。但是,只有ASDAS(AUC = 0.696,p = 0.040)在第24周显着预测ASAS20响应。在第一次英夫利昔单抗输注后,在第12周12和24(Wald X〜2 = 6.87,P = 0.009,P = 0.009和沃尔德X〜2 = 5.171,P = 0.023)。结论。英夫利昔单抗显示出活性非显影轴向脊柱型关节炎患者的效率。 ASDAS得分和第一剂量反应可以帮助预测英夫利昔单抗治疗在这些患者中的临床疗效。

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