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Detection of anti-Helicobacter py/oriantibodies in serum and duodenal fluid in peptic gastroduodenal disease

机译:消化性十二指肠疾病血清和十二指肠液中抗幽门螺杆菌/原抗体的检测

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AIM: To study the diagnosis of Helicobacter pylori (H pylori) infection through the determination of serum levels of anti-H pylori IgG and IgA antibodies, and the levels of anti-H pylori IgA antibodies in duodenal fluid. METHODS: Data were collected from 93 patients submitted to upper digestive endoscopy due to dyspeptic symptoms. The patients were either negative (group A) or positive (group B) to H pylori by means of both histological detection and urease tests. Before endoscopy, peripheral blood was collected for the investigation of anti-H pylori IgG and IgA antibodies. To perform the urease test, biopsies were obtained from the gastric antrum. For the histological evaluation, biopsies were collected from the gastric antrum (greater and lesser curvatures) and the gastric body. Following this, duodenal fluid was collected from the first and second portions of the duodenum. For the serological assaying of anti-H pylori IgG and IgA, and anti-H pylori IgA. in duodenal fluids, the ELISA method was utilized. RESULTS: The concentration of serum IgG showed sensitivity of 64.0%, specificity of 83.7%, positive predictive value of 82.0%, negative predictive value of 66.6% and accuracy of 73.1% for the diagnosis of H pylori infection. For the same purpose, serum IgA showed sensitivity of 72.0%, specificity of 65.9%, positive predictive value of 72.0%, negative predictive value of 67.4% and accuracy of 69.8%. If the serological tests were considered together, i.e. when both were positive or negative, the accuracy was 80.0%, sensitivity was 86.6%, specificity was 74.2%, positive predictive value was 74.2% and negative predictive value was 86.6%. When values obtained in the test for detecting IgA in the duodenal fluid were analyzed, no significant difference (P = 0.43) was observed between the values obtained from patients with or without H pylori infection. CONCLUSION: The results of serum IgG and IgA tests for H pylori detection when used simultaneously, are more efficient in accuracy, sensitivity and negative predictive value, than those when used alone. The concentration of IgA antibodies in duodenal fluid is not useful in identifying patients with or without H pylori.
机译:目的:通过测定血清中抗幽门螺杆菌IgG和IgA抗体的水平,以及十二指肠液中抗幽门螺杆菌IgA抗体的水平,来研究幽门螺杆菌感染的诊断。方法:收集了93例因消化不良症状而接受上消化内镜检查的患者的数据。通过组织学检测和脲酶测试,患者对幽门螺杆菌呈阴性(A组)或阳性(B组)。在内窥镜检查之前,收集外周血以研究抗幽门螺杆菌IgG和IgA抗体。为了进行尿素酶测试,从胃窦获得活组织检查。为了进行组织学评估,从胃窦(较大和较小的曲率)和胃体收集活检组织。此后,从十二指肠的第一和第二部分收集十二指肠液。用于抗H幽门IgG和IgA以及抗H幽门IgA的血清学检测。在十二指肠液中,采用了ELISA方法。结果:血清IgG检测对幽门螺杆菌感染的敏感性为64.0%,特异性为83.7%,阳性预测值为82.0%,阴性预测值为66.6%,准确度为73.1%。出于相同的目的,血清IgA的敏感性为72.0%,特异性为65.9%,阳性预测值为72.0%,阴性预测值为67.4%,准确度为69.8%。如果同时考虑血清学检测,即当两者均为阳性或阴性时,准确度为80.0%,敏感性为86.6%,特异性为74.2%,阳性预测值为74.2%,阴性预测值为86.6%。当分析在十二指肠液中检测IgA的测试中获得的值时,从有或没有幽门螺杆菌感染的患者获得的值之间未观察到显着差异(P = 0.43)。结论:与单独使用相比,血清IgG和IgA检测可同时检测H幽门螺旋杆菌,其准确性,敏感性和阴性预测值更为有效。十二指肠液中IgA抗体的浓度对鉴定是否患有幽门螺杆菌无效。

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