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Affiliations
Olga Sjomina
Institute of Clinical and Preventive Medicine, University of Latvia; Faculty of Medicine, University of Latvia
Jelizaveta Pavlova
Institute of Clinical and Preventive Medicine, University of Latvia; Faculty of Medicine, University of Latvia
Ilva Daugule
Institute of Clinical and Preventive Medicine, University of Latvia; Faculty of Medicine, University of Latvia
Pavel Janovic
Faculty of Medicine, University of Latvia
Ilze Kikuste
Institute of Clinical and Preventive Medicine, University of Latvia; Department of Research, Riga East University Hospital
Aigars Vanags
Department of Research, Riga East University Hospital
Ivars Tolmanis
Department of Research, Riga East University Hospital
Dace Rudzite
Institute of Clinical and Preventive Medicine, University of Latvia; Faculty of Medicine, University of Latvia
Inese Polaka
Institute of Clinical and Preventive Medicine, University of Latvia; Institute of Information Technology, Riga Technical University
Ilona Kojalo
Institute of Clinical and Preventive Medicine, University of Latvia; Faculty of Medicine, University of Latvia
Inta Liepniece-Karele
Institute of Clinical and Preventive Medicine, University of Latvia; Faculty of Medicine, University of Latvia; Academic Histology Laboratory
Sergejs Isajevs
Institute of Clinical and Preventive Medicine, University of Latvia; Faculty of Medicine, University of Latvia; Academic Histology Laboratory
Daiga Santare
Institute of Clinical and Preventive Medicine, University of Latvia; Faculty of Medicine, University of Latvia
Valdis Pirags
Institute of Clinical and Preventive Medicine, University of Latvia; Institute of Information Technology, Riga Technical University
Jelena Pahomova
Institute of Information Technology, Riga Technical University; P. Stradins Clinical Hospital
Vilnis Dzerve
Institute of Information Technology, Riga Technical University; P. Stradins Clinical Hospital
Lilian Tzivian
Institute of Clinical and Preventive Medicine, University of Latvia
Andrejs Erglis
Institute of Clinical and Preventive Medicine, University of Latvia; Institute of Information Technology, Riga Technical University; P. Stradins Clinical Hospital
Marcis Leja
Institute of Clinical and Preventive Medicine, University of Latvia; Faculty of Medicine, University of Latvia; Department of Research, Riga East University Hospital; Digestive Diseases Centre Gastro
How to Cite
Pepsinogen Test for the Evaluation of Precancerous Changes in Gastric Mucosa: a Population-Based Study
- Olga Sjomina ,
- Jelizaveta Pavlova ,
- Ilva Daugule ,
- Pavel Janovic ,
- Ilze Kikuste ,
- Aigars Vanags ,
- Ivars Tolmanis ,
- Dace Rudzite ,
- Inese Polaka ,
- Ilona Kojalo ,
- Inta Liepniece-Karele ,
- Sergejs Isajevs ,
- Daiga Santare ,
- Valdis Pirags ,
- Jelena Pahomova ,
- Vilnis Dzerve ,
- Lilian Tzivian ,
- Andrejs Erglis ,
- Marcis Leja
Abstract
Aims: The aim of the study was to evaluate the rationale of blood pepsinogen (PG) testing in population based screening settings.
Methods: Participants from a cross-sectional population-based study of cardiovascular risk factors in Latvia were invited to participate in the current study. Pepsinogen I and II were measured in blood samples taken during the initial study and at follow-up; upper gastrointestinal endoscopy was performed. There were three groups of patients: with moderately decreased (PG I< 70 ng/ml and PG I/PG II ratio < 3), with strongly decreased (PG I< 30 ng/ml and PG I/PG II ratio < 2), and with normal PG level. Biopsy with H. pylori detection was performed (updated Sydney system).
Results: Results from 259 patients were analyzed. Pepsinogens were decreased in 133 (51.4%), H. pylori was positive in 177 (66.0%) cases. Mean age was significantly lower in patients with normal compared to strongly decreased PG level group (52.8 vs. 64.1 years, p<0.001). Prevalence of severe corpus atrophy was higher in the strongly decreased compared to the normal PG test group: 7.0% vs. 0%; the same tendency was noted in the distribution of OLGA stages III-IV – 10.5% and 0.0%, OLGIM stages III-IV – 3.5% and 0%, and low-grade dysplasia – 15.8% and 2.4% (p<0.05). Two cases of gastric cancer were found; both presented decreased PG levels. A strong association between H. pylori eradication and PG ratio dynamics was found (p<0.05).
Conclusions: All high-risk lesions were found in the decreased PG test groups; two cancer cases were revealed.
However, PG demonstrated low specificity and low value of repeated testing. The value of PG as a sole test for gastric cancer risk is limited.