Bile Reflux Gastropathy and Functional Dyspepsia

The pathoetiology of functional dyspepsia remains unclear; one mechanism could be chemical gastropathy from chronic bile reflux. We aim to examine the association of bile reflux gastropathy with functional dyspepsia and identify predisposing factors. In a retrospective study, patients with functiona...

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Veröffentlicht in:Journal of neurogastroenterology and motility 2021, 27(3), , pp.400-407
Hauptverfasser: Lake, Andrew, Rao, Satish S C, Larion, Sebastian, Spartz, Helena, Kavuri, Sravan
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Sprache:eng
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Zusammenfassung:The pathoetiology of functional dyspepsia remains unclear; one mechanism could be chemical gastropathy from chronic bile reflux. We aim to examine the association of bile reflux gastropathy with functional dyspepsia and identify predisposing factors. In a retrospective study, patients with functional dyspepsia (Rome III) who completed symptom assessment, esophagogastroduodenoscopy, and biopsies were categorized into 3 groups; bile gastropathy (BG), non-bile gastropathy (NBG), and no gastropathy (NG). Demographics, symptoms, endoscopy, and motility data were compared between groups. Multivariate analysis identified clinical factors associated with BG. Of 262 patients (77.5% female), 90 had BG, 121 had NBG, and 51 had NG. Baseline demographics were similar, however, patients with BG reported significantly more severe abdominal pain than NBG or NG groups ( = 0.018). Gastric erythema was significantly more common in BG vs NBG groups ( < 0.001). Cholecystectomy was significantly associated (OR, 6.6; = 0.003) with the presence of gastropathy in BG compared to NBG or NG group. Patients with cholecystectomy had significantly more severe abdominal pain ( < 0.05), gastric erythema ( < 0.03), and gastritis ( < 0.05), and were more likely to be prescribed narcotic medications ( < 0.004) than patients without cholecystectomy. s Bile reflux gastropathy is associated with functional dyspepsia and causes more severe symptoms. Cholecystectomy predisposes to BG and abnormal pain, and could contribute to the pathogenesis of functional dyspepsia.
ISSN:2093-0879
2093-0887
DOI:10.5056/jnm20102