Objective: This study aims to investigate the clinical, endoscopic, biologic and histopathological differences between Helicobacter pylori-associated and autoimmune gastric atrophy.
Methods: A retrospective analysis was conducted on 95 patients diagnosed with either H. pylori-related corporal and antral atrophy (43 patients) or autoimmune corporal atrophic gastritis (52 patients).
Results: A significant male predisposition for H. pylori-associated atrophic changes in both the antrum and corpus regions (p=0.007, OR=3.24) was observed in comparison with autoimmune etiology of atrophy. While comorbidities and lifestyle factors showed similar distributions across groups, only unintentional self-reported weight loss demonstrated a significant association with H. pylori atrophy (p=0.0177, OR=3.94). Corporal erosions were strongly associated with antral and corporeal atrophic gastritis (p=0.04, OR=8.27), but the rest of mucosal lesions are comparable among groups. Interestingly, patients with H. pylori-related pangastric atrophy exhibited lower frequencies of altered triglyceride (p=0.018) and cholesterol (p=0.029) levels compared to the autoimmune group. Linear regression analysis identified low triglyceride levels as an independent predictor for H. pylori-associated antral and corporal atrophic gastritis (p=0.04) in endoscopic population with atrophy, but no hematological or clinical parameters were predictive for these changes.
Conclusions: Male patients are more likely to present with corpus atrophic gastritis associated with H. pylori infection than with an autoimmune etiology. Patients with atrophic gastritis tend to have similar clinical characteristics, except for dyslipidemia, which is more prevalent in those with H. pylori pangastritis. Corporal erosions are associated with active H. pylori infection in atrophic mucosa.
Tag Archives: atrophic gastritis
Chromoendoscopy and Magnification for the Evaluation of the Intragastric Extent of Atrophic Gastritis and Intestinal Metaplasia
Introduction: The detection of intragastric extent and progression of atrophic gastritis and intestinal metaplasia are mandatory in order to quantify the risk of development of the gastric cancer. The aim of the study is to assess the clinical value of magnifying endoscopy and chromoendoscopy in the evaluation of the intragastric extent of atrophic gastritis and intestinal metaplasia.
Material and methods: We performed magnifying chromoendoscopy with methylene blue and we identified modified patterns corresponding to premalignant gastric lesions. We studied the intragastric extent of these lesions. Biopsy specimens were taken from modified areas in order to confirm the presence of atrophic gastritis and intestinal metaplasia.
Results: We identified specific pit patterns for atrophic gastritis and intestinal metaplasia. In 21 patients (30%) these lesions were confined to gastric antrum. In 7 cases (17.5%), lesions were extended in gastric corpus. These patients were selected for further endoscopic surveillance.
Conclusions: Magnifying endoscopy and chromoendoscopy allow the detection of intragastric extent of intestinal metaplasia and atrophic gastritis. This could help to a better selection of patients for surveillance endoscopy.