Background
We aimed to assess a serological biopsy using five stomach-specific circulating biomarkers pepsinogen I (PGI), PGII, PGI/II ratio, anti- Helicobacter pylori (H. pylori) antibody, and gastrin-17 (G-17) for identifying high-risk individuals and predicting risk of developing gastric cancer (GC).
Results
In the cross-sectional analysis, PGII, the PG ratio, G17, anti- H. pylori IgG were associated with the presence of CAG, and the five biomarkers combined prediction is more effective than single factor prediction (0.692 vs 0.54, 0.604, 0.616, 0.629).
Conclusion
The combination of pepsinogens, G17 and anti-H. pylori antibodies for serological analysis is helpful to screen CAG high-risk individuals from the general population and recommend that these people should carry out further endoscopy and biopsy.
Figure 1
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Posted 23 Mar, 2021
On 23 Mar, 2021
On 19 Mar, 2021
On 18 Mar, 2021
On 18 Mar, 2021
On 18 Mar, 2021
Posted 23 Mar, 2021
On 23 Mar, 2021
On 19 Mar, 2021
On 18 Mar, 2021
On 18 Mar, 2021
On 18 Mar, 2021
Background
We aimed to assess a serological biopsy using five stomach-specific circulating biomarkers pepsinogen I (PGI), PGII, PGI/II ratio, anti- Helicobacter pylori (H. pylori) antibody, and gastrin-17 (G-17) for identifying high-risk individuals and predicting risk of developing gastric cancer (GC).
Results
In the cross-sectional analysis, PGII, the PG ratio, G17, anti- H. pylori IgG were associated with the presence of CAG, and the five biomarkers combined prediction is more effective than single factor prediction (0.692 vs 0.54, 0.604, 0.616, 0.629).
Conclusion
The combination of pepsinogens, G17 and anti-H. pylori antibodies for serological analysis is helpful to screen CAG high-risk individuals from the general population and recommend that these people should carry out further endoscopy and biopsy.
Figure 1
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