Analyzing serological screening of the functional state of gastric mucosa in clinical practice
https://doi.org/10.20538/1682-0363-2024-2-21-27
Abstract
Aim. To analyze the results of the GastroPanel and GastroScreen-3 tests over a 15-year follow-up and determine the incidence of autoimmune gastritis (AIG) in clinical practice and in a random sample of Novosibirsk residents.
Materials and methods. Biomarkers were analyzed in two groups: 1,742 people, average age of 50.0 ± 13.53 years (GastroPanel test, Biohit Oy, Finland), and 170 people, average age of 53.8 ± 12.89 years (GastroScreen-3 test, Vector-Best, Russia), from 2007 to 2022. The AIG incidence was calculated in current clinical practice and in a random sample of Novosibirsk residents aged 45–69 years. The PGI level of 160 µg / l was taken as the upper limit of normal, PGI of 31–50 µg / l indicated moderate atrophy, PGI < 30 µg / l and the PGI / PGII ratio ≤ 3 indicated severe gastric fundus atrophy. AIG was considered at PGI ≤ 10.1 μg / l, the PGI / PGI ratio ≤ 1.3, and gastrin-17 ≥ 42.4 pmol / l (GastroPanel) and at PGI ≤ 16.8 μg / l and the PGI / PGII ratio ≤ 1.5 (GastroScreen-3). The H. pylori IgG level > 42 EIU was considered to be positive. Antibodies to CagA protein were determined using the HelicoBest Antibody test (Vector-Best, Novosibirsk).
Results. Serological signs of severe and moderate gastric fundus atrophy were detected in 10 and 9.4% (GastroPanel test) and in 13.3 and 7% (GastroScreen-3 test) of those examined, respectively. Signs of multifocal atrophy were found in 0.7% of cases. Antibodies to H. pylori were detected in 57.7%, CagA+ strain – in 56.1% of cases. Peptic ulcer disease (PGI ≥160 µg / l) was found in 15.3% (GastroPanel test) and 10% (GastroScreen-3 test) of the examined. According to the GastroPanel and GastroScreen-3 tests, the incidence of AIG was 1.6% in a random sample and 2.6 and 3.5% in current clinical practice, respectively.
Conclusion. Twenty percent of the examined persons were at risk of developing gastric cancer and 10–15% had peptic ulcer disease, which requires further examination. The incidence of AIG in different study groups based on serological screening was 1.6–3.5%.
Keywords
About the Authors
A. V. BelkovetsRussian Federation
175/1, B. Bogatkova Str., Novosibirsk, 630089;
52, Krasny Prospect, Novosibirsk, 630091
Competing Interests:
The authors declare the absence of obvious or potential conflict of interest related to the publication of this article
N. V. Ozhiganova
Russian Federation
175/1, B. Bogatkova Str., Novosibirsk, 630089
Competing Interests:
The authors declare the absence of obvious or potential conflict of interest related to the publication of this article
M. V. Kruchinina
Russian Federation
175/1, B. Bogatkova Str., Novosibirsk, 630089;
52, Krasny Prospect, Novosibirsk, 630091
Competing Interests:
The authors declare the absence of obvious or potential conflict of interest related to the publication of this article
Ya. V. Polonskaya
Russian Federation
175/1, B. Bogatkova Str., Novosibirsk, 630089
Competing Interests:
The authors declare the absence of obvious or potential conflict of interest related to the publication of this article
L. V. Shcherbakova
Russian Federation
175/1, B. Bogatkova Str., Novosibirsk, 630089
Competing Interests:
The authors declare the absence of obvious or potential conflict of interest related to the publication of this article
References
1. Tu H., Sun L., Dong X., Gong Y., Xu Q., Jing J. et al. Serological Biopsy Using Five Stomach-Specific Circulating Biomarkers for Gastric Cancer Risk Assessment: A Multi-Phase Study. Am. J. Gastroenterol. 2017;112(5):704–715. DOI: 10.1038/ajg.2017.55.
2. Syrjänen K. Accuracy of Serum Biomarker Panel (GastroPanel®) in the Diagnosis of Atrophic Gastritis of the Corpus. Systematic Review and Meta-analysis. Anticancer Res. 2022;42(4):1679–1696. DOI: 10.21873/anticanres.15645.
3. Di Mario F., Cavallaro L.G., Moussa A.M., Caruana P., Merli R., Maini A. et al. Usefulness of serum pepsinogens in Helicobacter pylori chronic gastritis: relationship with inflammation, activity, and density of the bacterium. Dig. Dis. Sci. 2006;51(10):1791–1795. DOI: 10.1007/s10620-006-9206-1.
4. Agréus L., Kuipers E.J., Kupcinskas L., Malfertheiner P., Di Mario F., Leja M. et al. Rationale in diagnosis and screening of atrophic gastritis with stomach-specific plasma biomarkers. Scand. J. Gastroenterol. 2012;47(2):136–147. DOI: 10.3109/00365521.2011.645501.
5. Di Mario F., Franzoni L., Franceschi M., Rodriguez-Castro K.I., Russo M., Crafa P. Low levels of G17 and Barrett esophagus: a clinical relationship. Clin. Chem. Lab. Med. 2022;28:60(7):e165-e167. DOI: 10.1515/cclm-2022-0362.
6. Malfertheiner P., Megraud F., Rokkas T., Gisbert J.P., Liou J.M., Schulz C. et al. European Helicobacter and Microbiota Study group. Management of Helicobacter pylori infection: the Maastricht VI/Florence consensus report. Gut. 2022;2022:327745. DOI: 10.1136/gutjnl-2022-327745.
7. Kurilovich S., Belkovets A., Reshetnikov O., Openko T., Malyutina S., Ragino Y. et al. Stomach-specific Biomarkers (GastroPanel) Can Predict the Development of Gastric Cancer in a Caucasian Population: A Longitudinal Nested Case-Control Study in Siberia. Anticancer Res. 2016;36(1):247–253.
8. Пюрвеева К.В., Лапина Т.Л., Ивашкин В.Т., Коньков М.Ю., Склянская О.А., Серова А.Г., Васильева Н.Ю. Значение сывороточных показателей пепсиногена I, пепсиногена II и гастрина-17 в диагностике атрофического гастрита. Российский журнал гастроэнтерологии, гепатологии, колопроктологии. 2005;15(3):48–51.
9. Storskrubb T., Aro P., Ronkainen J., Sipponen P., Nyhlin H., Talley N.J. et al. Serum biomarkers provide an accurate method for diagnosis of atrophic gastritis in a general population: The Kalixanda study. Scand. J. Gastroenterol. 2008;43(12):1448–1455. DOI: 10.1080/00365520802273025. PMID: 18663663.
10. Biohit HealthCare. GastroPanel. URL: https://www.gastropanel.com/healthcare-professionals-and-laboratories/forms-and-instructions
11. Белковец А.В., Кручинина М.В., Ожиганова Н.В., Щербакова Л.В. Клинико-лабораторные особенности аутоиммунного гастрита в Сибири. Современная наука: актуальные проблемы теории и практики. Серия: Естественные и технические науки. 2022;(12):116–121. DOI: 10.37882/2223-2966.2022.12.03.
12. International Agency for Research on Cancer, World Health Organization. Schistosomiasis, liver flukes and Helicobacter pylori. IARC working group on the evaluation of carcinogenic risks to human. Monogr. Eval. Carcinog. Risks Hum. 1994;61:218–220.
13. El Hafa F., Wang T., Ndifor V.M., Jin G. Association between Helicobacter pylori antibodies determined by multiplex serology and gastric cancer risk: A meta-analysis. Helicobacter. 2022;27(3):e12881. DOI: 10.1111/hel.12881.
14. Kishikawa H., Ojiro K., Nakamura K., Katayama T., Arahata K., Takarabe S. et al. Previous Helicobacter pylori infection-induced atrophic gastritis: A distinct disease entity in an understudied population without a history of eradication. Helicobacter. 2020;25(1):e12669. DOI: 10.1111/hel.12669.
15. Kokkola A., Kosunen T.U., Puolakkainen P., Sipponen P., Harkonen M., Laxen F. et al. Spontaneous disappearance of Helicobacter pylori antibodies in patients with advanced atrophic corpus gastritis. APMIS. 2003;111(6):619–624. DOI: 10.1034/j.1600-0463.2003.1110604.x.
16. Magris R., De Re V., Maiero S., Fornasarig M., Guarnieri G., Caggiari L. et al. Low pepsinogen I/II ratio and high gastrin-17 levels typify chronic atrophic autoimmune gastritis patients with gastric neuroendocrine tumors. Clin. Transl. Gastroenterol. 2020;11(9):e00238. DOI: 10.14309/ctg.0000000000000238.
17. Ogutmen Koc D., Bektas S. Serum pepsinogen levels and OLGA/OLGIM staging in the assessment of atrophic gastritis types. Postgrad. Med. J. 2022;98(1160):441–445. DOI: 10.1136/postgradmedj-2020-139183.
18. Sugano K., Tack J., Kuipers E.J., Graham D.Y., El-Omar E.M., Miura S. et al. Kyoto global consensus report on Helicobacter pylori gastritis. Gut. 2015;64(9):1353–1367. DOI: 10.1136/gutjnl-2015-309252
19. Ивашкин В.Т., Маев И.В., Лапина Т.Л., Федоров Е.Д., Шептулин А.А., Трухманов А.С. и др. Клинические рекомендации Российской гастроэнтерологической ассоциации и ассоциации «Эндоскопическое общество РЭНДО» по диагностике и лечению гастрита, дуоденита. Российский журнал гастроэнтерологии, гепатологии, колопроктологии. 2021;31(4):70–99. DOI: 10.22416/1382-4376-2021-31-4-70-99.
20. Fernandez-Botran R., Wellmann I.A., Une C., Méndez-Chacón E., Hernández de Rodas E., Bhandari B. et al. Seroprevalence of Helicobacter pylori/CagA antibodies in guatemalan gastric cancer patients: association of seropositivity with increased plasma levels of pepsinogens but not soluble urokinase plasminogen activator receptor. Am. J. Trop. Med. Hyg. 2020;103(1):260–265. DOI: 10.4269/ajtmh.19-0934.
21. Rugge M., Savarino E., Sbaraglia M., Bricca L., Malfertheiner P. Gastritis: The clinico-pathological spectrum. Dig. Liver Dis. 2021;53(10):1237–1246. DOI: 10.1016/j.dld.2021.03.007.
22. Bakulina N., Tikhonov S., Malkov V., Vorobyev S., Belyakov I., Peshkova N. et al. Non-invasive screening of autoimmune atrophic gastritis in asymptomatic subjects by serological biomarker test (GastroPanel®). Anticancer Res. 2022;42(3):1517–1526. DOI: 10.21873/anticanres.15624.
23. Notsu T., Adachi K., Mishiro T., Fujihara H., Toda T., Takaki S. et al. Prevalence of autoimmune gastritis in individuals undergoing medical checkups in Japan. Intern. Med. 2019;58(13):1817–1823. DOI: 10.2169/internalmedicine.2292-18.
Review
For citations:
Belkovets A.V., Ozhiganova N.V., Kruchinina M.V., Polonskaya Ya.V., Shcherbakova L.V. Analyzing serological screening of the functional state of gastric mucosa in clinical practice. Bulletin of Siberian Medicine. 2024;23(2):21-27. https://doi.org/10.20538/1682-0363-2024-2-21-27