Increased risk of fundic gland polyps during long-term proton pump inhibitor therapyJalving, M., Koornstra, J. J., Wesseling, J., Boezen, H. M., De Jong, S. & Kleibeuker, J. H., 1-Nov-2006, In : Alimentary Pharmacology & Therapeutics. 24, 9, p. 1341-1348 8 p.
Research output: Contribution to journal › Article › Academic › peer-review
Background It is controversial whether proton pump inhibitor use leads to fundic gland polyp development.
Aim To determine whether fundic gland polyp development is due to proton pump inhibitor use and to investigate mechanisms involved.
Methods Proton pump inhibitor use and the presence of fundic gland polyps were assessed in consecutive patients undergoing oesophagogastroduodenoscopy. Biopsies from fundic gland polyps and gastric mucosa were taken. Dysplasia was graded as negative, low or high grade. Prevalence of parietal cell hyperplasia and parietal cell protrusions and the proportional cystic area were assessed.
Results 599 patients participated, 322 used proton pump inhibitors, 107 had fundic gland polyps. Long-term proton pump inhibitor use was associated with an increased risk of fundic gland polyps (1-4.9 years use: OR 2.2, 95% CI: 1.3-3.8; >= 5 years: OR 3.8, 95% CI: 2.2-6.7) while short-term therapy (<1 year) was not (OR 1.0, 95% CI: 0.5-1.8). Low-grade dysplasia was found in one fundic gland polyp. Fundic gland polyps associated with long-term proton pump inhibitor use had a larger proportional cystic area and higher frequency of parietal cell hyperplasia and parietal cell protrusion.
Conclusions Long-term proton pump inhibitor use is associated with an up to fourfold increase in the risk of fundic gland polyps. Risk of dysplasia is negligible. Aetiologically, these polyps seem to arise because of parietal cell hyperplasia and parietal cell protrusions resulting from acid suppression.
|Number of pages||8|
|Journal||Alimentary Pharmacology & Therapeutics|
|Publication status||Published - 1-Nov-2006|
- FAMILIAL ADENOMATOUS POLYPOSIS, PARIETAL-CELL PROTRUSIONS, GASTRIC POLYPS, EPITHELIAL DYSPLASIA, OMEPRAZOLE THERAPY, COLI GENE, STOMACH, MUTATIONS, FREQUENCY, ARTICLE