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Cited 37 time in webofscience Cited 39 time in scopus
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Distinct metaplastic and inflammatory phenotypes in autoimmune and adenocarcinoma-associated chronic atrophic gastritisopen access

Authors
Jeong, S.Choi, E.Petersen, C.P.Roland, J.T.Federico, A.Ippolito, R.D'Armiento, F.P.Nardone, G.Nagano, O.Saya, H.Romano, M.Goldenring, J.R.
Issue Date
Feb-2017
Publisher
SAGE Publications Ltd
Keywords
CD44 variant 9; DMBT1; gastritis; intestinal metaplasia; macrophage; neutrophil; Spasmolytic polypeptide-expressing metaplasia
Citation
United European Gastroenterology Journal, v.5, no.1, pp 37 - 44
Pages
8
Indexed
SCIE
SCOPUS
Journal Title
United European Gastroenterology Journal
Volume
5
Number
1
Start Page
37
End Page
44
URI
https://scholarworks.gnu.ac.kr/handle/sw.gnu/77789
DOI
10.1177/2050640616644142
ISSN
2050-6406
2050-6414
Abstract
Background: Autoimmune gastritis (AIG) and adenocarcinoma-associated chronic atrophic gastritis (CAG) are both associated with oxyntic atrophy, but AIG patients demonstrate an increased risk of carcinoid tumors rather than the elevated risk of adenocarcinoma observed with CAG. We therefore sought to compare the characteristics of the metaplastic mucosa in AIG and CAG patients. Methods: We examined markers for metaplasia (spasmolytic polypeptide expressing metaplasia (SPEM) and intestinal metaplasia) as well as proliferation (Ki67) and immune cell populations (neutrophils, macrophages, and eosinophils) in gastric sections from 16 female patients with autoimmune thyroiditis and AIG and 17 patients with CAG associated with gastric adenocarcinoma. Results: Both AIG and CAG patients demonstrated prominent SPEM and intestinal metaplasia. However, AIG patients displayed significantly lower numbers of infiltrating macrophages and significantly reduced mucosal cell proliferation as compared to CAG patients. Conclusions: These findings indicate that, while both AIG and CAG patients display prominent oxyntic atrophy and metaplasia, the AIG patients do not show proliferative metaplastic lineages that would predispose to adenocarcinoma. © 2016, © Author(s) 2016.
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