Low‐grade duodenal eosinophilia is associated with cagA in Helicobacter pylori‐related dyspepsia

Abstract Background and Aim Functional dyspepsia (FD) is a multifactorial disorder. Helicobacter pylori ( H. pylori )‐related dyspepsia (HpD) may be considered a separate entity. Duodenal eosinophilia is a potential pathogenic mechanism in FD. However, the impact of duodenal eosinophilia and H. pylori virulence genes in HpD was not explored. We aim to evaluate the association of H. pylori virulence genes and low‐grade duodenal eosinophilia in HpD. Methods A multi‐center cross‐sectional study was conducted. A total of 301 patients who meet Rome‐III criteria were selected before upper endoscopy, and 95 patients were included after normal endoscopy and positive H. pylori in gastric biopsies were assessed. Clinical parameters, H. pylori virulence genes ( cagA , oipA , and vacA ) and duodenal histology were evaluated. Results Sixty‐nine (72%) patients had epigastric pain syndrome (EPS), 17 (18%) post‐prandial distress syndrome (PDS) and 9 (10%) EPS/PDS overlap. FD syndromes were not associated with cagA or oipA strains. A significantly trend of vacA s1/m1 (78%) and s1/m2 (80%) positive strains in EPS was observed. Histological duodenal grading of chronic inflammation, low‐grade duodenal eosinophilia and intra‐epithelial lymphocytes showed no difference in oipA and vacA strains. Low‐grade duodenal eosinophilia was significant in cagA positive strain, and the OR for low‐grade duodenal eosinophilia with H. pylori cagA positive strain was 4.2 (95% CI, 1.78–9.93). Adjusting for age, gender, smoking, diabetes, alcohol, PPI, and NSAID, the OR was 5.44 (1.989–14.902). Conclusion Our findings suggest that low‐grade duodenal eosinophilia is significantly associated with cagA strain in HpD.