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Diagnostic value of anti-human citrullinated fibrinogen ELISA and comparison with four other anti-citrullinated protein assays

机译:抗人瓜氨酸化纤维蛋白原ELISA的诊断价值以及与其他四种抗瓜氨酸化蛋白测定的比较

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摘要

We studied the diagnostic performance of the anti-human citrullinated fibrinogen antibody (AhFibA) ELISA for rheumatoid arthritis (RA) in a consecutive cohort (population 1) and evaluated the agreement between the AhFibA ELISA and four other assays for anti-citrullinated protein/peptide antibodies (ACPAs) as well as rheumatoid factor in patients with longstanding RA (population 2). Population 1 consisted of 1024 patients with rheumatic symptoms; serum samples from these patients were sent to our laboratory for ACPA testing within the context of a diagnostic investigation for RA. Ninety-two of these patients were classified as having RA according to the American College of Rheumatology criteria and 463 were classified as non-RA patients. Population 2 consisted of 180 patients with longstanding RA and was used to assess agreement and correlations between five ACPA assays: anti-cyclic citrullinated peptide (CCP)1 and anti-CCP2 antibodies were detected using a commercially available ELISA, AhFibA using ELISA, and anti-PepA and anti-PepB antibodies using line immunoassay. Applying previously proposed cut-offs for AhFibA, we obtained a sensitivity of 60.9% and a specificity of 98.7% in population 1. Receiver operating characteristic curve analysis could not detect a significant difference in diagnostic performance between the AhFibA ELISA and anti-CCP2 assay. Performing a hierarchical nearest neighborhood cluster analysis of the five different ACPA assays in population 2, we identified two clusters: a cluster of anti-pepA, anti-pepB and anti-CCP1, and a cluster of AhFibA and anti-CCP2. In conclusion, we found that AhFibA and anti-CCP2 antibodies had similar diagnostic performance. However, disagreement between ACPA tests may occur.
机译:我们研究了连续队列(人群1)中抗人瓜氨酸化纤维蛋白原抗体(AhFibA)ELISA对类风湿性关节炎(RA)的诊断性能,并评估了AhFibA ELISA和其他四种抗瓜氨酸化蛋白/肽测定的一致性患有长期RA的患者中的抗体(ACPAs)和类风湿因子(人群2)。人口1包括1024名风湿病患者。这些患者的血清样本在RA诊断调查的范围内被送往我们的实验室进行ACPA测试。根据美国风湿病学会的标准,这些患者中的92名被归类为RA,463名被归​​类为非RA患者。人群2由180位长期RA的患者组成,用于评估五种ACPA分析之间的一致性和相关性:使用市售ELISA检测抗环瓜氨酸肽(CCP)1和抗CCP2抗体,使用ELISA检测AhFibA,并使用抗-PepA和抗PepB抗体使用线免疫分析。应用先前提议的AhFibA临界值,我们在人群1中获得了60.9%的敏感性和98.7%的特异性。接收器工作特征曲线分析无法检测到AhFibA ELISA和抗CCP2分析之间的诊断性能有显着差异。对人群2中的五种不同ACPA分析进行分层最近邻聚类分析,我们确定了两个聚类:抗pepA,抗pepB和抗CCP1聚类以及AhFibA和抗CCP2聚类。总之,我们发现AhFibA和抗CCP2抗体具有相似的诊断性能。但是,ACPA测试之间可能会出现分歧。

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