Shirin H, Bruck R, Kenet G, Krepel Z, Wardi J, Reif S, Zaidel L, Geva D, Avni Y, Halpern Z
Department of Gastroenterology, The E. Wolfson Medical Center, Holon, Israel.
J Gastroenterol. 1999 Feb;34(1):7-10. doi: 10.1007/s005350050209.
To determine the diagnostic value of a new serum and whole blood serological IgG antibody test, FlexPack HP, for the diagnosis of Helicobacter pylori in elderly symptomatic patients.
94 consecutive symptomatic patients who underwent upper endoscopy were studied (mean age, 62.6 years). On endoscopy, the presence of H. pylori infection was examined by biopsies from gastric antrum and body for rapid urease test and histologic examination. Blood was drawn prior to endoscopy and both blood and serum were immediately analyzed for human IgG antibodies to H. pylori by a new commercially available qualitative immunochromatographic method, FlexPack HP. This test incorporates high-molecular weight cell-associated proteins (HM-CAP), which are highly specific for H. pylori IgG antibodies.
Overall agreement for FlexPack HP whole blood vs FlexPack HP serum was 100%, and agreement with biopsy results was 71%. The gold standard (detection of H. pylori by histology or urease test) identified H. pylori in 61 patients (65%). Complete agreement was observed between the gold standard test and the serology kit in 72% (68/94) of sera (51 positive and 17 negative). Disagreement was found in sera of 26 patients; 16 sera were negative by the gold standard and positive by FlexPack HP and 10 patients were found negative by serology. The sensitivity of FlexPack HP was 84% and the specificity 52% when compared with the gold standard.
FlexPack HP serum and whole blood test is a simple and reliable method for the detection of H. pylori antibodies, with 100% agreement between the serum and blood results. In the elderly symptomatic patients the sensitivity of FlexPack HP was similar to that of other serologic tests, but the specificity was relatively low, limiting its use in this population.
确定一种新的血清和全血血清学IgG抗体检测方法FlexPack HP对老年有症状患者幽门螺杆菌诊断的价值。
对94例连续接受上消化道内镜检查的有症状患者(平均年龄62.6岁)进行研究。在内镜检查时,从胃窦和胃体取活检组织进行快速尿素酶试验和组织学检查,以检测幽门螺杆菌感染情况。在内镜检查前采集血液,采用一种新的商业化定性免疫层析方法FlexPack HP立即对血液和血清进行人抗幽门螺杆菌IgG抗体分析。该检测方法包含对幽门螺杆菌IgG抗体具有高度特异性的高分子量细胞相关蛋白(HM-CAP)。
FlexPack HP全血检测与FlexPack HP血清检测的总体一致性为100%,与活检结果的一致性为71%。金标准(通过组织学或尿素酶试验检测幽门螺杆菌)在61例患者(65%)中检测到幽门螺杆菌。在72%(68/94)的血清中(51份阳性和17份阴性),金标准检测与血清学试剂盒之间观察到完全一致。在26例患者的血清中发现不一致;16份血清金标准检测为阴性而FlexPack HP检测为阳性,10例患者血清学检测为阴性。与金标准相比,FlexPack HP的敏感性为84%,特异性为52%。
FlexPack HP血清和全血检测是一种简单可靠的检测幽门螺杆菌抗体的方法,血清和血液结果之间的一致性为100%。在老年有症状患者中,FlexPack HP的敏感性与其他血清学检测相似,但特异性相对较低,限制了其在该人群中的应用。