The Impact of Duodenal Mucosal Vulnerability in the Development of Epigastric Pain Syndrome in Functional Dyspepsia

• Published in: International journal of molecular sciences Vol. 23; no. 22; p. 13947
• Main Authors: Okata, Tomoki, Asanuma, Kiyotaka, Nakagawa, Kenichiro, Hatta, Waku, Koike, Tomoyuki, Imatani, Akira, Masamune, Atsushi
• Format: Journal Article
• Language: English
• Published: Switzerland MDPI AG 12.11.2022; MDPI
• Subjects: Abdomen; acid; Acid resistance; Acids; Biopsy; Body mass index; duodenal mucosa; Duodenum; Dyspepsia; Electrical resistivity; epigastric pain syndrome; Humans; Immunoglobulins; Inflammation; Lymphocytes; Mast cells; Mucosa; mucosal vulnerability; Pain; Pathogenesis; Patients; Plasma cells; Postprandial Period; Potassium; Reagents; Small intestine; Syndrome; transepithelial electrical resistance; acid; duodenal mucosa; epigastric pain syndrome; transepithelial electrical resistance; mucosal vulnerability
• ISSN: 1422-0067; 1661-6596; 1422-0067
• DOI: 10.3390/ijms232213947

An unidentified cause of functional dyspepsia (FD) is closely associated with medication resistance. Acid suppression is a traditional and preferential method for the treatment of FD, but the efficacy of this treatment varies between epigastric pain syndrome (EPS) and postprandial syndrome (PDS): it is efficient in the former but not much in the latter. Transepithelial electrical resistance (TEER), a surrogate of mucosal barrier function, was measured under pH 3 and pH 5 acidic conditions using duodenal biopsy specimens obtained from the patients with EPS and PDS and asymptomatic healthy controls. The infiltration of inflammatory cells to the duodenal mucosa was accessed by immunohistochemical analysis. The duodenal mucosal TEER in EPS patients was decreased by exposure to the acidic solution compared to that of the controls and the PDS patients. The decrease in TEER of the EPS patients was observed even under pH 5 weak acidic condition and was correlated to degree of the epigastric pain. Moreover, the duodenal mucosa of EPS patients presented an increase in mast cells and plasma cells that expressed Ig-E. Duodenal mucosal vulnerability to acid is likely to develop EPS.