Effects of refluxate pH values on duodenogastroesophageal reflux-induced esophageal adenocarcinoma
Effects of refluxate pH values on duodenogastroesophageal reflux-induced esophageal adenocarcinoma作者机构:Department of Gastroenterology First Hospitalof Zhengzhou University Zhengzhou 450052 Henan ProvinceChina Department of Gastroenterology Second Hospitalof Xi'an Jiao Tong University Xi'an 450052 Shanxi ProvinceChina
出 版 物:《World Journal of Gastroenterology》 (世界胃肠病学杂志(英文版))
年 卷 期:2011年第17卷第25期
页 面:3060-3065页
核心收录:
学科分类:090502[农学-动物营养与饲料科学] 0905[农学-畜牧学] 08[工学] 09[农学] 0815[工学-水利工程]
基 金:Supported by the Key Project of Clinical Medicine Ministry of Health No. 20012130
主 题:Esophageal reflux Esophageal adenocar-cinoma pH-metry Pathogenesis
摘 要:AIM: To determine the effects of duodenogastric juice pH on the development of esophageal adenocarcinoma (EAC). METHODS: An animal model of duodenogastroesophageal reflux was established using Sprague-Dawley (SD) rats undergoing esophagoduodenostomy (ED). The development of EAC was investigated in rats exposed to duodenogastric juice of different pH. The rats were di- vided into three groups: Iow-pH group (group A), high- pH group (group B) and a sham-operated group as a control (group C) (n = 30 rats in each group). The inci- dence of esophagitis, Barrett's esophagus (BE), intestinal metaplasia with dysplasia and EAC was observed 40 wk after the treatment. RESULTS: The incidence rate of esophagitis, BE, intestinal metaplasia with dysplasia and EAC was higher in groups A and B compared with the control group after 40 wk (P 〈 0.01), being 96% and 100% (P 〉 0.05), 88% and 82.4% (P 〉 0.05), 20% and 52.1% (P 〈 0.05), and 8% and 39% (P 〈 0.05), respectively. CONCLUSION: Non-acidic refluxate increases the occurrence of intestinal metaplasia with dysplasia and EAC while the Iow-pH gastric juice exerts a protective effect in the presence of duodenal juice. The non-acid reflux is particularly important in the progression from BE to cancer. Therefore, control of duodenal reflux may be an important prophylaxis for EAC.