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Journal of Clinical Pathology logoLink to Journal of Clinical Pathology
. 1990 Dec;43(12):981–986. doi: 10.1136/jcp.43.12.981

Gastric epithelium in the duodenum: its association with Helicobacter pylori and inflammation.

J I Wyatt 1, B J Rathbone 1, G M Sobala 1, T Shallcross 1, R V Heatley 1, A T Axon 1, M F Dixon 1
PMCID: PMC502969  PMID: 2266184

Abstract

Duodenal biopsy specimens from 471 adults and 47 children were examined to determine the prevalence and distribution of gastric epithelium in the duodenal bulb in relation to age, gender, gastroduodenal inflammation, smoking, alcohol and consumption of nonsteroidal anti-inflammatory drugs (NSAID). Gastric metaplasia was present in the anterior wall duodenal biopsy specimen in 31%, was significantly less common in patients under 17 than in adults, and was more common in males than females. In sixty two adults who underwent multiple radial duodenal biopsy gastric metaplasia was randomly distributed around the duodenal circumference; sixty three per cent of the patients with gastric metaplasia found on multiple biopsy were detected by just the anterior biopsy. Gastric metaplasia was not obviously associated with alcohol, cigarette, or NSAID consumption. While the presence of gastric metaplasia was associated with adulthood, male sex, and low fasting gastric juice pH, its extent was associated with active duodenitis and Helicobacter-associated gastritis. On logistic regression, gastric metaplasia in the duodenum and gastric Helicobacter pylori were independent predictors of active duodenitis, but were not significantly associated with inactive duodenal inflammation. H pylori was observed in duodenal biopsy specimens from 32 patients, all with active duodenitis; bacteria were present only on foci of gastric metaplasia, and were more likely to be seen when the metaplasia was extensive. It is proposed that inflammatory injury to the duodenal mucosa by H pylori may stimulate the development of further gastric metaplasia, and that the area of duodenum susceptible to colonisation with H pylori may therefore increase progressively until mucosal integrity is compromised and ulceration supervenes.

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Selected References

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  1. Blaser M. J. Gastric Campylobacter-like organisms, gastritis, and peptic ulcer disease. Gastroenterology. 1987 Aug;93(2):371–383. doi: 10.1016/0016-5085(87)91028-6. [DOI] [PubMed] [Google Scholar]
  2. Bransom C. J., Boxer M. E., Palmer K. R., Clark J. C., Underwood J. C., Duthie H. L. Mucosal cell proliferation in duodenal ulcer and duodenitis. Gut. 1981 Apr;22(4):277–282. doi: 10.1136/gut.22.4.277. [DOI] [PMC free article] [PubMed] [Google Scholar]
  3. Carrick J., Lee A., Hazell S., Ralston M., Daskalopoulos G. Campylobacter pylori, duodenal ulcer, and gastric metaplasia: possible role of functional heterotopic tissue in ulcerogenesis. Gut. 1989 Jun;30(6):790–797. doi: 10.1136/gut.30.6.790. [DOI] [PMC free article] [PubMed] [Google Scholar]
  4. Frierson H. F., Jr, Caldwell S. H., Marshall B. J. Duodenal bulb biopsy findings for patients with non-ulcer dyspepsia with or without Campylobacter pylori gastritis. Mod Pathol. 1990 May;3(3):271–276. [PubMed] [Google Scholar]
  5. Gaskin R. J., Gad A., Barros D'sa A. A., Joffe S. N., Baron J. H. Natural history and morphology of secretagogue-induced duodenal ulcers in rats. Gastroenterology. 1975 Oct;69(4):903–910. [PubMed] [Google Scholar]
  6. Gastric spiral bacteria. Lancet. 1984 Jul 14;2(8394):100–101. [PubMed] [Google Scholar]
  7. Graham D. Y. Campylobacter pylori and peptic ulcer disease. Gastroenterology. 1989 Feb;96(2 Pt 2 Suppl):615–625. doi: 10.1016/s0016-5085(89)80057-5. [DOI] [PubMed] [Google Scholar]
  8. Gray S. F., Wyatt J. I., Rathbone B. J. Simplified techniques for identifying Campylobacter pyloridis. J Clin Pathol. 1986 Nov;39(11):1279–1279. doi: 10.1136/jcp.39.11.1279-a. [DOI] [PMC free article] [PubMed] [Google Scholar]
  9. Gregory M. A., Spitaels J. M. Variations in the morphology of villous epithelial cells within 8 mm of untreated duodenal ulcers. J Pathol. 1987 Oct;153(2):109–119. doi: 10.1002/path.1711530204. [DOI] [PubMed] [Google Scholar]
  10. Hara M., Harasawa S., Tani N., Miwa T., Tsutsumi Y. Gastric metaplasia in duodenal ulcer. Histochemical considerations of its pathophysiological significance. Acta Pathol Jpn. 1988 Aug;38(8):1011–1018. doi: 10.1111/j.1440-1827.1988.tb02373.x. [DOI] [PubMed] [Google Scholar]
  11. Jenkins D., Goodall A., Gillet F. R., Scott B. B. Defining duodenitis: quantitative histological study of mucosal responses and their correlations. J Clin Pathol. 1985 Oct;38(10):1119–1126. doi: 10.1136/jcp.38.10.1119. [DOI] [PMC free article] [PubMed] [Google Scholar]
  12. Joffe S. N., Lee F. D., Blumgart L. H. Duodenitis. Clin Gastroenterol. 1978 Sep;7(3):635–650. [PubMed] [Google Scholar]
  13. Lev R., Thomas E., Parl F. F., Pitchumoni C. S. Pathological and histomorphometric study of the effects of alcohol on the human duodenum. Digestion. 1980;20(3):207–213. doi: 10.1159/000198441. [DOI] [PubMed] [Google Scholar]
  14. Marshall B. J., Goodwin C. S., Warren J. R., Murray R., Blincow E. D., Blackbourn S. J., Phillips M., Waters T. E., Sanderson C. R. Prospective double-blind trial of duodenal ulcer relapse after eradication of Campylobacter pylori. Lancet. 1988 Dec 24;2(8626-8627):1437–1442. doi: 10.1016/s0140-6736(88)90929-4. [DOI] [PubMed] [Google Scholar]
  15. Marshall B. J., McGechie D. B., Rogers P. A., Glancy R. J. Pyloric Campylobacter infection and gastroduodenal disease. Med J Aust. 1985 Apr 15;142(8):439–444. doi: 10.5694/j.1326-5377.1985.tb113444.x. [DOI] [PubMed] [Google Scholar]
  16. Paoluzi P., Pallone F., Palazzesi P., Marcheggiano A., Iannoni C. Frequency and extent of bulbar duodenitis in duodenal ulcer, endoscopic and histological study. Endoscopy. 1982 Nov;14(6):193–195. doi: 10.1055/s-2007-1021619. [DOI] [PubMed] [Google Scholar]
  17. Parrish J. A., Rawlins D. C. Intestinal mucosa in the Zollinger-Ellison syndrome. Gut. 1965 Jun;6(3):286–289. doi: 10.1136/gut.6.3.286. [DOI] [PMC free article] [PubMed] [Google Scholar]
  18. Patrick W. J., Denham D., Forrest A. P. Mucous change in the human duodenum: a light and electron microscopic study and correlation with disease and gastric acid secretion. Gut. 1974 Oct;15(10):767–776. doi: 10.1136/gut.15.10.767. [DOI] [PMC free article] [PubMed] [Google Scholar]
  19. RHODES J. EXPERMENTAL PRODUCTION OF GASTRIC EPITHELIUM IN THE DUODENUM. Gut. 1964 Oct;5:454–458. doi: 10.1136/gut.5.5.454. [DOI] [PMC free article] [PubMed] [Google Scholar]
  20. Rathbone B. J., Wyatt J. I., Heatley R. V. Possible pathogenetic pathways of Campylobacter pylori in gastro-duodenal disease. Scand J Gastroenterol Suppl. 1988;142:40–43. [PubMed] [Google Scholar]
  21. Shousha S., Barrison I. G., El-Sayeed W., Khan S., Parkins R. A. A study of incidence and relationship of intestinal metaplasia of gastric antrum and gastric metaplasia of duodenum in patients with nonulcer dyspepsia. Dig Dis Sci. 1984 Apr;29(4):311–316. doi: 10.1007/BF01318515. [DOI] [PubMed] [Google Scholar]
  22. Shousha S., Spiller R. C., Parkins R. A. The endoscopically abnormal duodenum in patients with dyspepsia: biopsy findings in 60 cases. Histopathology. 1983 Jan;7(1):23–34. doi: 10.1111/j.1365-2559.1983.tb02213.x. [DOI] [PubMed] [Google Scholar]
  23. Tatsuta M., Iishi H., Yamamura H., Yamamoto R., Taniguchi H. Enhancement by tetragastrin of experimental induction of gastric epithelium in the duodenum. Gut. 1989 Mar;30(3):311–315. doi: 10.1136/gut.30.3.311. [DOI] [PMC free article] [PubMed] [Google Scholar]
  24. Wyatt J. I., Rathbone B. J., Dixon M. F., Heatley R. V., Axon A. T. Campylobacter pylori and development of duodenal ulcer. Lancet. 1988 Jan 16;1(8577):118–119. doi: 10.1016/s0140-6736(88)90315-7. [DOI] [PubMed] [Google Scholar]
  25. Wyatt J. I., Rathbone B. J., Dixon M. F., Heatley R. V. Campylobacter pyloridis and acid induced gastric metaplasia in the pathogenesis of duodenitis. J Clin Pathol. 1987 Aug;40(8):841–848. doi: 10.1136/jcp.40.8.841. [DOI] [PMC free article] [PubMed] [Google Scholar]

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