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

Author:

Guo Xiaopei1,Schreurs Marco W. J.2,Marijnissen Fleur E.1,Mommersteeg Michiel C.1,Nieuwenburg Stella A. V.1,Doukas Michail3,Erler Nicole S.45,Capelle Lisette G.6,Bruno Marco J.1,Peppelenbosch Maikel P.1ORCID,Spaander Manon C. W.1ORCID,Fuhler Gwenny M.1ORCID

Affiliation:

1. Department of Gastroenterology and Hepatology, Erasmus MC, 3015 GD Rotterdam, The Netherlands

2. Department of Immunology, Erasmus MC, 3015 GD Rotterdam, The Netherlands

3. Department of Pathology, Erasmus MC, 3015 GD Rotterdam, The Netherlands

4. Department of Biostatistics, Erasmus MC, 3015 GD Rotterdam, The Netherlands

5. Department of Epidemiology, Erasmus MC, 3015 GD Rotterdam, The Netherlands

6. Department of Gastroenterology and Hepatology, Meander Medical Center, 3813 TZ Amersfoort, The Netherlands

Abstract

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.

Publisher

MDPI AG

Subject

General Medicine

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