首页> 外文期刊>Annals of the Rheumatic Diseases: A Journal of Clinical Rheumatology and Connective Tissue Research >Serum markers associated with clinical improvement in patients with ankylosing spondylitis treated with golimumab
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Serum markers associated with clinical improvement in patients with ankylosing spondylitis treated with golimumab

机译:戈利木单抗治疗强直性脊柱炎患者的血清标志物与临床改善相关

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Objective: Identify serum biomarkers modulated by golimumab treatment and associated with clinical response in patients with ankylosing spondylitis (AS). Methods: Sera were collected at weeks 0, 4 and 14 from 100 patients with active AS in the GO-RAISE study. Patients were randomly assigned subcutaneous injections of placebo, golimumab 50 mg, or golimumab 100 mg every 4 weeks. Samples were tested for select inflammatory, bone and cartilage markers, and protein profiling was also performed. Results: Golimumab treatment resulted in significant decreases in several serum proteins at weeks 4 and 14 compared with placebo. Patients who achieved clinical response at week 14, as assessed by a ≥20% improvement in the Assessment in SpondyloArthitis international Society response criteria (ASAS 20), demonstrated a distinct biomarker profile with lower levels of acute phase reactants and inflammatory biomarkers compared with patients who did not. Notably, combinations of two or three biomarkers assessed at baseline were predictive of various clinical outcomes (ASAS 20, Bath ankylosing spondylitis disease activity index 50 or Bath ankylosing spondylitis functional index) using a logistic regression analysis, and the overall predictive values for these combined biomarkers were greater than observed for C-reactive protein (CRP) alone. Conclusion: Golimumab modulated acute phase reactants and inflammatory markers in patients with active AS. Specific combinations of biomarkers at baseline demonstrated a stronger prediction for clinical efficacy than CRP alone. These data provide insights into the mechanism of golimumab on inflammatory processes driving AS pathology, and may have utility in managing the treatment of patients with AS.
机译:目的:确定强直性脊柱炎(AS)患者接受戈利木单抗治疗后调节的血清生物标志物并与临床反应相关。方法:在GO-RAISE研究中于第0、4和14周从100例活动性AS患者中收集血清。每4周为患者随机分配皮下注射安慰剂,戈利木单抗50毫克或戈利木单抗100毫克。测试样品的选择性炎症,骨和软骨标志物,并进行蛋白质谱分析。结果:与安慰剂相比,戈利木单抗治疗导致第4周和第14周几种血清蛋白的显着降低。根据国际脊柱关节炎国际评估标准(ASAS 20)评估中≥20%的改善评估,在第14周获得临床反应的患者,与那些接受治疗的患者相比,表现出独特的生物标志物特征,其中急性期反应物和炎症生物标志物的水平较低没有。值得注意的是,在基线时评估的两种或三种生物标志物的组合可通过逻辑回归分析预测各种临床结局(ASAS 20,巴斯强直性脊柱炎疾病活动指数50或巴斯强直性脊柱炎功能指数),以及这些联合生物标志物的总体预测值大于单独的C反应蛋白(CRP)观察到的。结论:戈利木单抗调节活动性AS患者的急性期反应物和炎症标志物。基线时生物标志物的特定组合比单独的CRP证明对临床疗效的预测更强。这些数据提供了关于戈利木单抗驱动AS病理的炎症过程机制的见解,并可能在管理AS患者的治疗中具有效用。

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