The dynamics of the oesophageal squamous epithelium 'normalisation' process in patients with gastro‐oesophageal reflux disease treated with long‐term acid suppression or anti‐reflux surgery. Issue 10 (21st March 2017) - Mastracci, L.
Summary: Background: Proton pump inhibitors and laparoscopic anti‐reflux surgery (LARS) offer long‐term symptom control to patients with gastro‐oesophageal reflux disease (GERD). Aim: To evaluate the process of 'normalisation' of the squamous epithelium morphology of the distal oesophagus on these therapies. Methods: In the LOTUS trial, 554 patients with chronic GERD were randomised to receive either esomeprazole (20–40 mg daily) or LARS. After 5 years, 372 patients remained in the study (esomeprazole, 192; LARS, 180). Biopsies were taken at the Z‐line and 2 cm above, at baseline, 1, 3 and 5 years. A severity score was calculated based on: papillae elongation, basal cell hyperplasia, intercellular space dilatations and eosinophilic infiltration. The epithelial proliferative activity was assessed by Ki‐67 immunohistochemistry. Results: A gradual improvement in all variables over 5 years was noted in both groups, at both the Z‐line and 2 cm above. The severity score decreased from baseline at each subsequent time point in both groups ( P < 0.001, all comparisons), attaining a normal level by 5 years. Corresponding decreases in Ki‐67 expression were observed ( P < 0.001, all comparisons). No significant differences were found between esomeprazole treatment and LARS. Neither baseline severity score nor Ki‐67 expression predicted the risk of treatment failure. Conclusions: Five years of treatment is generally required before squamous epithelial cell morphology and proliferation are 'normalised' in patients with chronic GERD, despite endoscopic and symptomatic disease control. Control of the acid component of the refluxate seems to play the predominant role in restoring tissue morphology. Abstract : Linked Content This article is linked to Mastracci et al and Genta papers. To view these articles visithttps://doi.org/10.1111/apt.14097 andhttps://doi.org/10.1111/apt.14118 .