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Increased Prevalence of Autoimmune Gastritis in Patients with a Gastric Precancerous Lesion

Background: Autoimmune gastritis (AIG), characterized with the presence of anti-parietal-cell antibodies (APCA), is a risk factor for gastric cancer. However, AIG may go underdiagnosed, especially in the case of H. pylori infection and the presence of gastric precancerous lesions (GPL), due to the a...

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Autores principales: Guo, Xiaopei, Schreurs, Marco W. J., Marijnissen, Fleur E., Mommersteeg, Michiel C., Nieuwenburg, Stella A. V., Doukas, Michail, Erler, Nicole S., Capelle, Lisette G., Bruno, Marco J., Peppelenbosch, Maikel P., Spaander, Manon C. W., Fuhler, Gwenny M.
Formato: Online Artículo Texto
Lenguaje:English
Publicado: MDPI 2023
Materias:
Acceso en línea:https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573100/
https://www.ncbi.nlm.nih.gov/pubmed/37834796
http://dx.doi.org/10.3390/jcm12196152
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author Guo, Xiaopei
Schreurs, Marco W. J.
Marijnissen, Fleur E.
Mommersteeg, Michiel C.
Nieuwenburg, Stella A. V.
Doukas, Michail
Erler, Nicole S.
Capelle, Lisette G.
Bruno, Marco J.
Peppelenbosch, Maikel P.
Spaander, Manon C. W.
Fuhler, Gwenny M.
author_facet Guo, Xiaopei
Schreurs, Marco W. J.
Marijnissen, Fleur E.
Mommersteeg, Michiel C.
Nieuwenburg, Stella A. V.
Doukas, Michail
Erler, Nicole S.
Capelle, Lisette G.
Bruno, Marco J.
Peppelenbosch, Maikel P.
Spaander, Manon C. W.
Fuhler, Gwenny M.
author_sort Guo, Xiaopei
collection PubMed
description Background: Autoimmune gastritis (AIG), characterized with the presence of anti-parietal-cell antibodies (APCA), is a risk factor for gastric cancer. However, AIG may go underdiagnosed, especially in the case of H. pylori infection and the presence of gastric precancerous lesions (GPL), due to the ambiguous pathology and delayed symptom onset. Aim: Investigate the prevalence and characteristics of AIG in GPL patients. Methods: Prevalence of AIG was determined with the presence of APCA in patients with GPL (n = 256) and the control group (n = 70). Pathological characteristics and levels of gastrin 17 (G17), pepsinogen (PG) I and II and anti-Helicobacter pylori IgG were assessed in GPL cases, and the severity of intestinal metaplasia and gastric atrophy was scored by expert pathologists. Results: APCA positivity was observed in 18% of cases vs. 7% of controls (p = 0.033). Only 3/256 patients were previously diagnosed with AIG. The presence of APCA was associated with corpus-limited and extended GPL. A receiver operating curve analysis demonstrated that the G17 and PGI/II ratio could identify APCA-positive patients within GPL cases (AUC: 0.884). Conclusions: The prevalence of AIG is higher in patients with GPL but goes undiagnosed. Using G17 and PG I/II as diagnostic markers can help to identify patients with AIG and improve surveillance programs for patients with GPL.
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spelling pubmed-105731002023-10-14 Increased Prevalence of Autoimmune Gastritis in Patients with a Gastric Precancerous Lesion Guo, Xiaopei Schreurs, Marco W. J. Marijnissen, Fleur E. Mommersteeg, Michiel C. Nieuwenburg, Stella A. V. Doukas, Michail Erler, Nicole S. Capelle, Lisette G. Bruno, Marco J. Peppelenbosch, Maikel P. Spaander, Manon C. W. Fuhler, Gwenny M. J Clin Med Article Background: Autoimmune gastritis (AIG), characterized with the presence of anti-parietal-cell antibodies (APCA), is a risk factor for gastric cancer. However, AIG may go underdiagnosed, especially in the case of H. pylori infection and the presence of gastric precancerous lesions (GPL), due to the ambiguous pathology and delayed symptom onset. Aim: Investigate the prevalence and characteristics of AIG in GPL patients. Methods: Prevalence of AIG was determined with the presence of APCA in patients with GPL (n = 256) and the control group (n = 70). Pathological characteristics and levels of gastrin 17 (G17), pepsinogen (PG) I and II and anti-Helicobacter pylori IgG were assessed in GPL cases, and the severity of intestinal metaplasia and gastric atrophy was scored by expert pathologists. Results: APCA positivity was observed in 18% of cases vs. 7% of controls (p = 0.033). Only 3/256 patients were previously diagnosed with AIG. The presence of APCA was associated with corpus-limited and extended GPL. A receiver operating curve analysis demonstrated that the G17 and PGI/II ratio could identify APCA-positive patients within GPL cases (AUC: 0.884). Conclusions: The prevalence of AIG is higher in patients with GPL but goes undiagnosed. Using G17 and PG I/II as diagnostic markers can help to identify patients with AIG and improve surveillance programs for patients with GPL. MDPI 2023-09-23 /pmc/articles/PMC10573100/ /pubmed/37834796 http://dx.doi.org/10.3390/jcm12196152 Text en © 2023 by the authors. https://creativecommons.org/licenses/by/4.0/Licensee MDPI, Basel, Switzerland. This article is an open access article distributed under the terms and conditions of the Creative Commons Attribution (CC BY) license (https://creativecommons.org/licenses/by/4.0/).
spellingShingle Article
Guo, Xiaopei
Schreurs, Marco W. J.
Marijnissen, Fleur E.
Mommersteeg, Michiel C.
Nieuwenburg, Stella A. V.
Doukas, Michail
Erler, Nicole S.
Capelle, Lisette G.
Bruno, Marco J.
Peppelenbosch, Maikel P.
Spaander, Manon C. W.
Fuhler, Gwenny M.
Increased Prevalence of Autoimmune Gastritis in Patients with a Gastric Precancerous Lesion
title Increased Prevalence of Autoimmune Gastritis in Patients with a Gastric Precancerous Lesion
title_full Increased Prevalence of Autoimmune Gastritis in Patients with a Gastric Precancerous Lesion
title_fullStr Increased Prevalence of Autoimmune Gastritis in Patients with a Gastric Precancerous Lesion
title_full_unstemmed Increased Prevalence of Autoimmune Gastritis in Patients with a Gastric Precancerous Lesion
title_short Increased Prevalence of Autoimmune Gastritis in Patients with a Gastric Precancerous Lesion
title_sort increased prevalence of autoimmune gastritis in patients with a gastric precancerous lesion
topic Article
url https://www.ncbi.nlm.nih.gov/pmc/articles/PMC10573100/
https://www.ncbi.nlm.nih.gov/pubmed/37834796
http://dx.doi.org/10.3390/jcm12196152
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