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首页> 外文期刊>Journal of Clinical Microbiology >Evaluation of the performance of commercial test kits for detection of Helicobacter pylori antibodies in serum.
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Evaluation of the performance of commercial test kits for detection of Helicobacter pylori antibodies in serum.

机译:评估用于检测血清中幽门螺杆菌抗体的商业测试试剂盒的性能。

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We have compared the sensitivities, specificities, and predictive values of three commercial serological assays for the diagnosis of Helicobacter pylori infection. A qualitative latex method (Pyloriset; Orion Diagnostics), a semiquantitative enzyme-linked immunosorbent assay (ELISA) (GAP test IgG; Bio-Rad), and a quantiative ELISA (Helico-G; Porton Cambridge) were used in 109 untreated dyspeptic patients. The presence of H. pylori was established when the results of culture and/or histology of the gastric biopsies taken were positive. The prevalence of H. pylori infection was 62% (52% in 42 patients younger than 45 years of age and 69% in 67 patients older than 45 years of age). Sensitivities and specificities were 68 and 76% for Pyloriset, 89 and 77% for GAP test IgG, and 82 and 83% for Helico-G. The positive predictive values for all three tests were between 85 and 90%. The predictive values for the absence of disease with a negative result were 62, 82, and 74% for Pyloriset, the GAP test, and Helico-G, respectively. With Helico-G in the younger group (less than 45 years), sensitivity significantly lower (71 versus 87%) and a positive predictive value lower than those for the older group (greater than 45 years) were found. Either the sensitivities and specificities of commercial methods for the measurement of antibodies to H. pylori in serum must be improved or the relationship between the presence of antibodies and the presence of bacteria in the stomach at the time of investigation is too weak to allow the use of serological techniques instead of culture and histological investigation of gastric biopsy material.
机译:我们已经比较了三种商业血清学检测对幽门螺杆菌感染的诊断的敏感性,特异性和预测价值。在109例未经治疗的消化不良患者中使用了定性乳胶法(Pyloriset; Orion Diagnostics),半定量酶联免疫吸附测定(ELISA)(GAP测试IgG; Bio-Rad)和定量ELISA(Helico-G; Porton Cambridge) 。当所采集的胃活检的培养和/或组织学结果为阳性时,便确定了幽门螺杆菌的存在。幽门螺杆菌感染的患病率为62%(42岁以下,45岁以下的患者为52%,而67岁以上,45岁以上的患者为69%)。幽门螺杆菌的敏感性和特异性分别为68%和76%,GAP测试IgG的敏感性和特异性为89%和77%,Helico-G的敏感性和特异性为82%和83%。所有三个测试的阳性预测值在85%至90%之间。幽门螺杆菌,GAP试验和Helico-G的无疾病阴性结果的预测值分别为62%,82%和74%。在较年轻的组(少于45岁)中使用Helico-G,发现敏感性显着降低(分别为71%和87%),并且比较年长的组(大于45岁)的阳性预测值低。必须提高用于测量血清中幽门螺杆菌抗体的商业方法的敏感性和特异性,或者在研究时抗体的存在与胃中细菌的存在之间的关系太弱而无法使用血清学技术代替胃活检材料的培养和组织学研究。

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