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The Use of an Oral Fluid Immunoglobulin G ELISA for the Detection of Helicobacter pylori Infection in Children

机译:口服液免疫球蛋白G ELISA在检测儿童幽门螺杆菌感染中的应用

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Background. Enzyme linked immunosorbent assay (ELISA) evaluation of oral fluid immunoglobulin G (IgG) antibodies to Helicobacter pylori is a unique approach for both epidemiological studies and the diagnosis of infection, especially in children. The use of oral fluid sampling to evaluate specific H. pylori IgG antibodies has advantages over serum, including reduced biohazard risk and noninvasive collection. Oral fluid sampling is fast and involves minimal patient discomfort. Since children facilitate transmission of H. pylori infection, a simple, accurate, noninvasive diagnostic test is necessary for large epidemiologic studies. The aim of our study was to evaluate a new oral fluid ELISA for detection of IgG antibodies to H. pylori in children. Materials and methods. We compared this new oral fluid ELISA with the HM-CAP~(TM) serum ELISA and gastric biopsy histology using 779 oral fluid samples from children collected at 11 clinical sites across the United States. This cohort included 315 children symptomatic for abdominal pain and 464 asymptomatic. All samples were evaluated in a double blind manner. The oral fluid ELISA demonstrated a sensitivity of 76.2% and a specificity of 94.0% in children 2 months old to 20 1/2 years, as compared with the HM-CAP~(TM) serologic assay. The assay's sensitivity improved to 81.3% in children aged 5 or greater and the specificity remained at 94.0%. When compared with gastric biopsy histology in the same age group, the oral fluid ELISA demonstrated a sensitivity of 71.7% and a specificity of 90.4%. Results. This new oral fluid ELISA is moderately sensitive and offers a very specific method for detecting H. pylori infection in older children, but it is of little value in children under the age of 5 years. Conclusions. Overall, we conclude that this oral fluid ELISA does not appear to be a helpful clinical tool for the diagnosis of H. pylori infection in children.
机译:背景。酶联免疫吸附法(ELISA)评估针对幽门螺杆菌的口服液免疫球蛋白G(IgG)抗体是流行病学研究和感染诊断(尤其是儿童)的独特方法。使用口服液采样评估特异性幽门螺杆菌IgG抗体具有优于血清的优势,包括降低的生物危害风险和无创收集。口服液采样速度快,并且患者不适感最小。由于儿童促进了幽门螺杆菌感染的传播,因此对于大型流行病学研究,必须进行简单,准确,无创的诊断测试。我们研究的目的是评估一种新的口服液ELISA,以检测儿童幽门螺杆菌IgG抗体。材料和方法。我们比较了这种新的口服液ELISA与HM-CAP〜(TM)血清ELISA和胃活检组织学,使用了来自美国11个临床地点的儿童的779份口服液样品。该队列包括315名有症状的腹痛儿童和464名无症状的儿童。以双盲方式评估所有样品。与HM-CAP〜(TM)血清学检测相比,口服液ELISA在2个月至20 1/2岁的儿童中显示出76.2%的敏感性和94.0%的特异性。 5岁或以上儿童的测定灵敏度提高到81.3%,特异性保持在94.0%。与同一年龄组的胃活检组织学相比,口服液ELISA的敏感性为71.7%,特异性为90.4%。结果。这项新的口服液ELISA具有中等敏感性,为检测大龄儿童的幽门螺杆菌感染提供了一种非常特定的方法,但对于5岁以下的儿童却没有什么价值。结论。总的来说,我们得出的结论是,这种口服液ELISA似乎不是诊断儿童幽门螺杆菌感染的有用临床工具。

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