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荧光偏振分析法与目前用于诊断人类布鲁氏菌病的三种血清学检测方法的评估与比较

Evaluation and comparison of fluorescence polarization assay with three of the currently used serological tests in diagnosis of human brucellosis.

作者信息

Konstantinidis A, Minas A, Pournaras S, Kansouzidou A, Papastergiou P, Maniatis A, Stathakis N, Hadjichristodoulou C

机构信息

Department of Hygiene and Epidemiology, Medical School, University of Thessaly, 22 Papakiriazi Str., PC 41222, Larissa.

出版信息

Eur J Clin Microbiol Infect Dis. 2007 Oct;26(10):715-21. doi: 10.1007/s10096-007-0363-8.

Abstract

Fluorescence polarization assay (FPA) is a method that has been used for the diagnosis of brucellosis in animals for many years. To test its possible usefulness for the diagnosis of human brucellosis, 230 sera from patients with clinical signs of brucellosis and positive serological tests (Rose Bengal, Standard Agglutination Test, iELISA), and 305 sera from a healthy population with no clinical/epidemiological/serological evidence were examined with FPA. By using ROC analysis, the cut-off value was estimated at 99 mP, with 93.5% sensitivity (95% CI 89.5-96.3) and 96.1% specificity (95% CI 93.2-97.9). The pairwise comparison of ROC curves between FPA and iELISA and between FPA and RBT revealed no significant statistic difference (P < 0.05). On the contrary it revealed a significant statistic difference between FPA and SAT (P > 0.05). SAT also had the lowest sensitivity (81.7%) among the three tests used in case definition while iELISA had a sensitivity of 90.8% and RBT a sensitivity of 88.7%. The Kappa analysis showed that FPA has a very good agreement (0.92) with the "status of the disease" and with iELISA (0.837). According to our results, FPA seems to be a valuable method for the diagnosis of brucellosis in humans. Taking into consideration the advantages of the method such as the speed of results obtaining, the objectivity of results interpretation, as well as the cost, FPA could be considered as a replacement for other established methods. However, further studies are needed to assess the reproducibility of FPA.

摘要

荧光偏振分析(FPA)是一种多年来一直用于动物布鲁氏菌病诊断的方法。为了测试其在人类布鲁氏菌病诊断中的潜在用途,对230份来自有布鲁氏菌病临床症状且血清学检测呈阳性(虎红平板凝集试验、标准凝集试验、间接ELISA)的患者血清,以及305份来自无临床/流行病学/血清学证据的健康人群的血清进行了FPA检测。通过ROC分析,估计临界值为99 mP,灵敏度为93.5%(95%可信区间89.5 - 96.3),特异性为96.1%(95%可信区间93.2 - 97.9)。FPA与间接ELISA以及FPA与虎红平板凝集试验之间的ROC曲线两两比较未显示出显著的统计学差异(P < 0.05)。相反,FPA与标准凝集试验之间显示出显著的统计学差异(P > 0.05)。在病例定义中使用的三项检测中,标准凝集试验的灵敏度也最低(81.7%),而间接ELISA的灵敏度为90.8%,虎红平板凝集试验的灵敏度为88.7%。Kappa分析表明,FPA与“疾病状态”以及与间接ELISA具有非常好的一致性(0.92)和(0.837)。根据我们的结果,FPA似乎是一种用于人类布鲁氏菌病诊断的有价值的方法。考虑到该方法的优点,如结果获取速度、结果解释的客观性以及成本,FPA可被视为其他既定方法的替代方法。然而,需要进一步研究来评估FPA的可重复性。

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