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首页> 外文期刊>Annals of the New York Academy of Sciences >Clinical Evaluation of a New Quantitative Enzyme-Linked Immunosorbent Assay for Detection of Double-Stranded DNA Autoantibodies
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Clinical Evaluation of a New Quantitative Enzyme-Linked Immunosorbent Assay for Detection of Double-Stranded DNA Autoantibodies

机译:一种新型定量酶联免疫吸附法检测双链DNA自身抗体的临床评价

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The measurement of autoantibodies specific for doublestranded DNA (anti-dsDNA) is a useful tool for the diagnosis and the prognosis of systemic lupus erythematosus (SLE). A new quantitative enzyme-linked immunosorbent assay (ELISA), ORG anti-dsDNA, is recently available for the determination of anti-dsDNA antibodies. The aim of this study was to evaluate the clinical performance of this new assay in a cohort of SLE patients. Seventy-five sera from SLE patients were tested by two methods for anti-dsDNA determination, ORG anti-dsDNA, and EliA anti-dsDNA. Normal controls were 60 sera from healthy subjects. Moreover, 37 sera from patients with non-SLE connective tissue diseases were tested in parallel. The levels of complement components (C3, C4, CH50) were measured by nephelometry. From SLE patients, 91% were positive against 9% in non-SLE patients and 2% in healthy subjects. The sensitivity, specificity, and Youden test for SLE were 90%, 98%, and 88%, respectively. The Yule test (1%) indicated a close association with the disease. The comparison with EliA anti-dsDNA showed a moderate concordance between the two tests in the group of SLE (k = 0.51) and a good concordance in the non-SLE group (k = 0.89). A significant inverse correlation was found with complement components levels, biological markers associated with disease activity. Our results show this new assay as sensitive and specific for the diagnosis of SLE. Moreover, the correlation with markers associated with disease activity makes it promising for clinical use.
机译:对双链DNA(anti-dsDNA)特异的自身抗体的测量是诊断和预测系统性红斑狼疮(SLE)的有用工具。一种新的定量酶联免疫吸附测定(ELISA),即ORG抗dsDNA,最近可用于测定抗dsDNA抗体。这项研究的目的是评估这一新方法在一组SLE患者中的临床表现。通过两种抗dsDNA测定方法检测了SLE患者的75份血清,即ORG抗dsDNA和EliA抗dsDNA。正常对照是来自健康受试者的60份血清。此外,平行检测了非SLE结缔组织病患者的37份血清。补体成分(C3,C4,CH50)的水平通过浊度法测量。在SLE患者中,有91%的患者为阳性,而非SLE患者为9%,健康受试者为2%。 SLE的敏感性,特异性和Youden检验分别为90%,98%和88%。 Yule测试(1%)表明与疾病密切相关。与EliA抗dsDNA的比较显示,在SLE组中两次检测之间的适度一致性(k = 0.51),在非SLE组中良好的一致性(k = 0.89)。发现与补体成分水平,与疾病活动相关的生物学标志物显着负相关。我们的结果表明,这种新方法对SLE的诊断具有敏感性和特异性。而且,与疾病活动相关的标志物的相关性使其有望用于临床。

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