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10.18632/oncotarget.7981

http://scihub22266oqcxt.onion/10.18632/oncotarget.7981
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C5008368!5008368!26968951
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suck abstract from ncbi


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pmid26968951      Oncotarget 2016 ; 7 (16): 22397-408
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  • Serum Helicobacter pylori FliD antibody and the risk of gastric cancer #MMPMID26968951
  • Li H; Zhang B; Hu X; Dong Y; Fan Q; Guo F; Ren X; Zhou H; Tian W; Zhao Y
  • Oncotarget 2016[Apr]; 7 (16): 22397-408 PMID26968951show ga
  • FliD and CagA are important virulence factors of H. pylori. We aimed to evaluate the screening values of FliD and CagA for gastric cancer (GC). Serum samples were obtained from 232 cases and 266 controls in a case-control study. Unconditional multivariate logistic regression with odds ratios (ORs) and 95% confidence intervals (CIs) was used to analyze the relationships between FliD, CagA and GC. The sensitivities, specificities and receiver operating characteristic (ROC) curves were calculated. Finally, the combined screening values of FliD, FlaA, NapA and CagA were assessed based on discriminant analysis. In all subjects, the associations of FliD and CagA with GC were evident with ORs (95% CIs) of 7.6 (4.7-12.3) and 2.5 (1.6-3.8), respectively (*p<0.001). The areas under ROC curves (AUCs) for FliD and CagA were 0.800 and 0.653, respectively. The AUC for the combination of FliD, FlaA and NapA was 0.915, which represented an increase of 0.115 over that of FliD alone (*p<0.001). These findings indicate that the FliD antibody is associated with GC and could exhibit high validity as a biomarker in screening for GC patients. The combination of FliD, FlaA and NapA improved the screening validity.
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