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Diagnostic Accuracy of the E-Plate Serum Antibody Test Kit in Detecting Helicobacter pylori Infection Among Japanese Children

机译:E-板血清抗体检测试剂盒对日本儿童幽门螺杆菌感染的诊断准确性

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Background: A number of noninvasive diagnostic tests are available to detect Helicobacter pylori infection. Data on serologic testing of children are lacking, however, and thus it remains unclear whether the serology cutoff points used for adults are appropriate for children. Methods: Serum and stool samples were obtained from 73 children who visited 5 hospitals in Japan between March 1993 and December 2009. Analysis of stool samples was carried out using an H pylori stool antigen enzyme-linked immunosorbent assay (HpSA ELISA), and serum antibodies to H pylori were examined using an antibody determination kit (E-Plate Eiken H pylori antibody). The validity of the serologic test was evaluated based on its sensitivity, specificity, and receiver operating characteristics curve. Results: Of the 73 children included in this study, 34 were HpSA-positive and 39 were negative. Among the 34 HpSA-positive patients, 32 were IgG-positive and 2 were IgG-negative. Of the 39 patients who were HpSA-negative, 38 were IgG-negative and 1 was IgG-positive. The sensitivity, specificity, and positive likelihood ratio for IgG antibody testing were 91.2%, 97.4%, and 35.6, respectively, based on the recommended adult cutoff point of 10 U/ml. Among children, use of cutoff points in the range of 7 to 9 U/ml yielded optimal values for sensitivity and specificity, as well as a positive likelihood ratio. Conclusions: The performance of the E-plate anti-H pylori IgG antibody test was comparable to that of the stool antigen test and is therefore suitable for epidemiologic studies of H pylori infection in large samples.
机译:背景:许多非侵入性诊断测试可用于检测幽门螺杆菌感染。然而,缺乏关于儿童血清学检测的数据,因此,尚不清楚用于成人的血清学分界点是否适合儿童。方法:从1993年3月至2009年12月在日本5家医院就诊的73名儿童的血清和粪便样本中进行分析。粪便样本的分析采用幽门螺杆菌粪便抗原酶联免疫吸附试验(HpSA ELISA)和血清抗体进行。使用抗体测定试剂盒(E-Plate Eiken H幽门螺杆菌抗体)检查抗幽门螺杆菌的抗体。根据血清学检测的敏感性,特异性和受体工作特性曲线评估其有效性。结果:本研究纳入的73名儿童中,HpSA阳性34例,阴性39例。在34例HpSA阳性患者中,32例IgG阳性,2例IgG阴性。在39例HpSA阴性患者中,38例IgG阴性,1例IgG阳性。基于建议的成人临界值10 U / ml,IgG抗体检测的灵敏度,特异性和阳性可能性比分别为91.2%,97.4%和35.6。在儿童中,使用临界点在7至9 U / ml的范围内可获得灵敏度和特异性的最佳值,以及正似然比。结论:E板抗H幽门IgG抗体测试的性能与粪便抗原测试相当,因此适合于大样本H幽门感染的流行病学研究。

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