首页> 外文期刊>Japanese journal of infectious diseases >Accuracy of a Stick-Type Kit and Enzyme-Linked Immunosorbent Assay in Detecting Helicobacter pylori Antibodies in Urine of People Living in the Japan Sea Region of Northern Japan
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Accuracy of a Stick-Type Kit and Enzyme-Linked Immunosorbent Assay in Detecting Helicobacter pylori Antibodies in Urine of People Living in the Japan Sea Region of Northern Japan

机译:棒型试剂盒和酶联免疫吸附法在居住于日本北部日本海域的人的尿液中检测幽门螺杆菌抗体的准确性

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摘要

In Japan, both a stick-type kit and an enzyme-linked immunosorbent assay (ELISA) kit are available for the detection of antibodies to Helicobacter pylori in urine. However, the accuracy of these tests has not been fully examined in northern Japanese populations. Urine samples from 359 subjects were tested using a stick-type H. pylori-antibody detection kit (RAPIRUN), and urine samples from 201 subjects were tested using an ELISA-based test (URINELISA). The prevalence of H. pylori infection was determined by the 13C-urea breath test (UBT) and a monoclonal antibody-based stool antigen test (TPAg). Subjects were considered to have the infection if either the UBT or rapid TPAg results were positive. The percentage of positive test results for RAPIRUN and URINELISA was 54.0% and 40.8%, respectively. Sensitivity and specificity were 83.3% and 67.0%, respectively, for RAPIRUN and 86.5% and 85.8% for URINELISA. Nineteen subjects had cut-off index values of between 0.4 and 0.9 by URINELISA, and 4 of these subjects (21.1%) were found to be infected with H. pylori. The urine-based ELISA was more accurate than the rapid stick-type kit in these patients. If negative ELISA results are near the cut-off value, subjects should receive an additional test to determine whether they are infected with H. pylori.
机译:在日本,棒型试剂盒和酶联免疫吸附测定(ELISA)试剂盒都可用于检测尿液中的幽门螺杆菌抗体。但是,这些测试的准确性尚未在日本北部人口中得到充分检验。使用棒型幽门螺杆菌抗体检测试剂盒(RAPIRUN)测试了359位受试者的尿液样本,并使用了基于ELISA的测试(URINELISA)测试了201位受试者的尿液样本。幽门螺杆菌感染的患病率通过13C尿素呼气试验(UBT)和基于单克隆抗体的粪便抗原试验(TPAg)确定。如果UBT或快速TPAg结果呈阳性,则认为受试者已感染。 RAPIRUN和URINELISA阳性检测结果的百分比分别为54.0%和40.8%。 RAPIRUN的敏感性和特异性分别为83.3%和67.0%,URINELISA的敏感性和特异性分别为86.5%和85.8%。通过URINELISA,有19位受试者的截断指数值介于0.4到0.9之间,其中4位受试者(21.1%)被发现感染了幽门螺杆菌。在这些患者中,基于尿液的ELISA比快速棒式试剂盒更准确。如果ELISA阴性结果接近临界值,则受试者应接受另一项测试以确定他们是否感染了幽门螺杆菌。

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