Abstract
BACKGROUND: Barrett's esophagus (BE), a significant complication of gastro-esophageal reflux disease (GERD), is the single most important risk factor for esophageal adenocarcinoma. The strong association between BE and chronic GERD suggests that abnormal esophageal acid exposure plays a vital role in this condition. METHODS: Review on PPI treatment for Barrett's esophagus. RESULTS: The progression of BE from specialized intestinal metaplasia to dysplasia and finally invasive carcinoma is incompletely understood, but increased and disordered proliferation is a key cellular event. In both ex vivo experiments and clinical trials in humans, effective acid suppression scales down the proliferative activity of Barrett's metaplasia and the likelihood of dysplasia as well. Today, proton pump inhibitors (PPIs) are almost universally used for the management of reflux symptoms in patients with BE while they may offer many other benefits when used as single agents or in conjunction with pharmacologic or endoscopic therapies. Yet, acid suppression with these drugs may be suboptimal in many patients and their ultimate role in preventing cancer formation has not yet been proven. Because PPIs are life-long therapy for patients with BE, their potential drawbacks need to be reviewed and their relative value need to be balanced when compared to laparoscopic fundoplication. CONCLUSIONS: The ability of PPIs to suppress acid profoundly and consistently may be crucial in the long-term management of BE and esophageal cancer chemoprevention.
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