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评估类风湿关节炎疾病活动的新型多生物标志物检测的验证。

Validation of a novel multibiomarker test to assess rheumatoid arthritis disease activity.

机构信息

UAB Center for Education and Research on Therapeutics, UAB Arthritis Clinical Intervention Program, Division of Clinical Immunology and Rheumatology, University of Alabama at Birmingham, FOT 805D, 510 20th Street South, Birmingham, AL 35294, USA.

出版信息

Arthritis Care Res (Hoboken). 2012 Dec;64(12):1794-803. doi: 10.1002/acr.21767.

Abstract

OBJECTIVE

Quantitative assessment of disease activity in rheumatoid arthritis (RA) is important for patient management, and additional objective information may aid rheumatologists in clinical decision making. We validated a recently developed multibiomarker disease activity (MBDA) test relative to clinical disease activity in diverse RA cohorts.

METHODS

Serum samples were obtained from the Index for Rheumatoid Arthritis Measurement, Brigham and Women's Hospital Rheumatoid Arthritis Sequential Study, and Leiden Early Arthritis Clinic cohorts. Levels of 12 biomarkers were measured and combined according to a prespecified algorithm to generate the composite MBDA score. The relationship of the MBDA score to clinical disease activity was characterized separately in seropositive and seronegative patients using Pearson's correlations and the area under the receiver operating characteristic curve (AUROC) to discriminate between patients with low and moderate/high disease activity. Associations between changes in MBDA score and clinical responses 6-12 weeks after initiation of anti-tumor necrosis factor or methotrexate treatment were evaluated by the AUROC.

RESULTS

The MBDA score was significantly associated with the Disease Activity Score in 28 joints using the C-reactive protein level (DAS28-CRP) in both seropositive (AUROC 0.77, P < 0.001) and seronegative (AUROC 0.70, P < 0.001) patients. In subgroups based on age, sex, body mass index, and treatment, the MBDA score was associated with the DAS28-CRP (P < 0.05) in all seropositive and most seronegative subgroups. Changes in the MBDA score at 6-12 weeks could discriminate both American College of Rheumatology criteria for 50% improvement responses (P = 0.03) and DAS28-CRP improvement (P = 0.002). Changes in the MBDA score at 2 weeks were also associated with subsequent DAS28-CRP response (P = 0.02).

CONCLUSION

Our findings establish the criterion and discriminant validity of a novel multibiomarker test as an objective measure of RA disease activity to aid in the management of RA in patients with this condition.

摘要

目的

类风湿关节炎(RA)疾病活动的定量评估对患者管理很重要,额外的客观信息可能有助于风湿病学家做出临床决策。我们验证了一种最近开发的多生物标志物疾病活动(MBDA)测试,该测试与不同 RA 队列中的临床疾病活动相关。

方法

从类风湿关节炎测量指数、布莱根妇女医院类风湿关节炎序贯研究和莱顿早期关节炎诊所队列中获得血清样本。测量了 12 种生物标志物的水平,并根据预设算法进行组合,生成复合 MBDA 评分。使用 Pearson 相关系数和接受者操作特征曲线下的面积(AUROC)分别在血清阳性和血清阴性患者中描述 MBDA 评分与临床疾病活动之间的关系,以区分低和中/高度疾病活动的患者。通过 AUROC 评估抗肿瘤坏死因子或甲氨蝶呤治疗开始后 6-12 周 MBDA 评分变化与临床反应之间的关系。

结果

MBDA 评分与血清阳性(AUROC 0.77,P < 0.001)和血清阴性(AUROC 0.70,P < 0.001)患者的 C 反应蛋白水平(DAS28-CRP)相关,均与 28 关节疾病活动评分(DAS28-CRP)显著相关。在基于年龄、性别、体重指数和治疗的亚组中,MBDA 评分与 DAS28-CRP 在所有血清阳性和大多数血清阴性亚组中均相关(P < 0.05)。6-12 周时 MBDA 评分的变化可以区分美国风湿病学会 50%改善反应的标准(P = 0.03)和 DAS28-CRP 改善(P = 0.002)。2 周时 MBDA 评分的变化也与随后的 DAS28-CRP 反应相关(P = 0.02)。

结论

我们的发现确立了一种新型多生物标志物测试的标准和判别有效性,作为 RA 疾病活动的客观测量指标,以帮助管理这种疾病的患者。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/0453/3556516/3963a4d040a7/acr0064-1794-f1.jpg

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