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Helicobacter pylori KatA and AhpC antibodies as novel biomarkers for gastric cancer

机译:幽门螺杆菌KatA和AhpC抗体作为胃癌的新型生物标志物

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AIM : To investigate catalase (KatA) and alkyl hydroperoxide reductase (AhpC) antibodies of Helicobacter pylori as biomarkers for gastric cancer (GC). METHODS : This study included 232 cases and 264 controls. Recombinant KatA and AhpC proteins were constructed and the levels of antibodies were tested by indirect enzyme-linked immunosorbent assay (ELISA). Logistic regression was applied to analyze the relationships between KatA, AhpC and GC. The χ2 trend test was used to evaluate the dose-response relationships between serum KatA and AhpC antibody levels and GC. Receiver operating characteristic (ROC) curve was used to evaluate the screening accuracy of KatA and AhpC as biomarkers. Combined analysis was used to observe screening accuracy of predictors for GC. RESULTS : In all subjects, the association between KatA and AhpC and GC risk was significant ( P < 0.001) with odds ratio (OR) = 12.84 (95%CI: 7.79-21.15) and OR = 2.4 (95%CI: 1.55-3.73), respectively. KatA and AhpC antibody levels were strongly related to GC risk with a dose-dependent effect ( P for trend < 0.001). The area under the ROC (AUC) for KatA was 0.806, providing a sensitivity of 66.81% and specificity of 86.36%; and the AUC for AhpC was 0.615, with a sensitivity of 75.65% and specificity of 45.49%. The AUC was 0.906 for KatA and flagella protein A (FlaA) combined analysis. CONCLUSION : Serum KatA and AhpC antibodies are associated with GC risk and KatA may serve as a biomarker for GC. KatA/FlaA combined analysis improved screening accuracy.
机译:目的:研究幽门螺杆菌的过氧化氢酶(KatA)和烷基氢过氧化物还原酶(AhpC)抗体作为胃癌(GC)的生物标志物。方法:本研究包括232例和264例对照。构建了重组的KatA和AhpC蛋白,并通过间接酶联免疫吸附测定(ELISA)测试了抗体的水平。应用逻辑回归分析KatA,AhpC和GC之间的关系。采用χ 2 趋势测试来评估血清KatA和AhpC抗体水平与GC之间的剂量反应关系。接收者操作特征(ROC)曲线用于评估KatA和AhpC作为生物标志物的筛选准确性。组合分析用于观察GC预测因子的筛选准确性。结果:在所有受试者中,KatA和AhpC与GC风险之间的关联均显着(P <0.001),优势比(OR)= 12.84(95%CI:7.79-21.15)和OR = 2.4(95%CI:1.55- 3.73)。 KatA和AhpC抗体水平与GC风险密切相关,并具有剂量依赖性效应(趋势<0.001,P)。 KatA的ROC(AUC)下面积为0.806,灵敏度为66.81%,特异性为86.36%; AhpC的AUC为0.615,灵敏度为75.65%,特异性为45.49%。 KatA和鞭毛蛋白A(FlaA)组合分析的AUC为0.906。结论:血清KatA和AhpC抗体与GC风险有关,KatA可作为GC的生物标志物。 KatA / FlaA组合分析提高了筛选准确性。

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