H.pylori peptic ulcer disease pathophysiology: Difference between revisions
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*The patients with higher gastric acid secretion have increased risk of developing duodenal ulcers compared to normal, healthy individuals. | *The patients with higher gastric acid secretion have increased risk of developing duodenal ulcers compared to normal, healthy individuals. | ||
*The most important requirements for the development of duodenal ulceration are: | *The most important requirements for the development of duodenal ulceration are: | ||
:*Gastric metaplasia in the proximal duodenum | |||
:*Gastric metaplasia in the proximal duodenum | :*Active chronic duodenitis | ||
====Pathogenesis==== | ====Pathogenesis==== | ||
'''Gastric metaplasia''' | '''Gastric metaplasia''' |
Revision as of 16:44, 12 January 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Yamuna Kondapally, M.B.B.S[2]
Overview
Pathophysiology
- H.pylori is closely associated with both duodenal and gastric ulcers.[1]
- The estimated lifetime risk for the development of peptic ulcer disease is 10-20%, in patients with H.pylori infection.
- H.pylori can be diagnosed in 60-100% of gastric ulcer patients and 90-100% in duodenal ulcer patients.
Duodenal Ulceration
- The patients with higher gastric acid secretion have increased risk of developing duodenal ulcers compared to normal, healthy individuals.
- The most important requirements for the development of duodenal ulceration are:
- Gastric metaplasia in the proximal duodenum
- Active chronic duodenitis
Pathogenesis
Gastric metaplasia
- H.pylori causes hypergastrinemia and increased sensitivity to gastrin.
- Gastric metaplasia (the presence of gastric-type mucus secreting cells in the surface epithelium of the duodenum) occurs as a part of host defence mechanism to protect against the repeated injury caused by arrival of unneutralized acid in the first part of duodenum.
References
- ↑ Kuipers EJ, Thijs JC, Festen HP (1995). "The prevalence of Helicobacter pylori in peptic ulcer disease". Aliment Pharmacol Ther. 9 Suppl 2: 59–69. PMID 8547530.