Risk factors associated with Barrett’s epithelial dysplasia
AIM:To elucidate risk factors associated with dysplasia of short-segment Barrett’s esophagus(BE).METHODS:A total of 151 BE patients who underwent endoscopic examination from 2004 to 2008 in Aoyama Hospital,Tokyo Women’s Medical University,Japan and whose diagnosis was confirmed from biopsy specimens...
Gespeichert in:
Veröffentlicht in: | World journal of gastroenterology : WJG 2014-04, Vol.20 (15), p.4353-4361 |
---|---|
Hauptverfasser: | , , , , , |
Format: | Artikel |
Sprache: | eng |
Schlagworte: | |
Online-Zugang: | Volltext |
Tags: |
Tag hinzufügen
Keine Tags, Fügen Sie den ersten Tag hinzu!
|
container_end_page | 4361 |
---|---|
container_issue | 15 |
container_start_page | 4353 |
container_title | World journal of gastroenterology : WJG |
container_volume | 20 |
creator | Fujita, Mikiko Nakamura, Yuri Kasashima, Saeko Furukawa, Maiko Misaka, Ryoichi Nagahara, Hikaru |
description | AIM:To elucidate risk factors associated with dysplasia of short-segment Barrett’s esophagus(BE).METHODS:A total of 151 BE patients who underwent endoscopic examination from 2004 to 2008 in Aoyama Hospital,Tokyo Women’s Medical University,Japan and whose diagnosis was confirmed from biopsy specimens were enrolled in the study.BE was diagnosed based on endoscopic findings of gastric-appearing mucosa or apparent columnar-lined esophagus proximal to the esophagogastric junction.Dysplasia was classified into three grades-mild,moderate and severe-according to the guidelines of the Vienna Classification System for gastrointestinal epithelial neoplasia.Anthropometric and biochemical data were analyzed to identify risk factors for BE dysplasia.The prevalence of Helicobacter pylori(H.pylori)infection and the expression of p53 by immunohistological staining were also investigated.RESULTS:Histological examination classified patients into three types:specialized columnar epithelium(SCE)(n=65);junctional(n=38);and gastric fundic(n =48).The incidence of dysplasia or adenocarcinoma from BE of the SCE type was significantly higher than that of the other two types(P<0.01).The univariate analysis revealed that sex,H.pylori infection,body weight,p53 overexpression,and low diastolic blood pressure(BP)were associated with BE dysplasia.In contrast,body mass index,waist circumference,metabolic syndrome complications,and variables related to glucose or lipid metabolism were not associated with dysplasia.Multivariate logistic analysis showed that overexpression of p53[odds ratio(OR)=13.1,P=0.004],H.pylori infection(OR=0.19,P=0.066),and diastolic BP(OR=0.87,P=0.021)were independent risk factors for epithelial dysplasia in BE patients with the SCE type.CONCLUSION:Overexpression of p53 is a risk factor for dysplasia of BE,however,H.pylori infection and diastolic BP inversely associated with BE dysplasia might be protective. |
doi_str_mv | 10.3748/wjg.v20.i15.4353 |
format | Article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3989971</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><cqvip_id>90888889504849524953485053</cqvip_id><sourcerecordid>1519263069</sourcerecordid><originalsourceid>FETCH-LOGICAL-c440t-1cc3380a74fbd01f556ea65bbc423587243236094b31810c3373acb5afadccb13</originalsourceid><addsrcrecordid>eNpVkM9q3DAQh0VpabZp7z0VH3vxdqSRLOnQQhv6DwKBkJ7FWJZ3lXrtjeRNyK2v0dfrk0RLtksrGASab34jPsZec1iilubd3fVqeStgGblaSlT4hC2E4LYWRsJTtuAAurYo9Al7kfM1gEBU4jk7EVI3stG4YO8vY_5Z9eTnKeWKcp58pDl01V2c19UnSinM859fv3MVtuUlDJGGqrvP24FypJfsWU9DDq8O9yn78eXz1dm3-vzi6_ezj-e1lxLmmnuPaIC07NsOeK9UE6hRbeulQGW0kCiwAStb5IZDgTWSbxX11HnfcjxlHx5zt7t2EzofxjnR4LYpbijdu4mi-78zxrVbTbcOrbFW7wPeHgLSdLMLeXabmH0YBhrDtMuOK25Fg9DYgsIj6tOUcwr9cQ0Ht7fuinVXrLti3e2tl5E3_37vOPBXcwHwkLmextVNHFdHxoLZH6tAGmmVKIXSKCixDyF5kBs</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1519263069</pqid></control><display><type>article</type><title>Risk factors associated with Barrett’s epithelial dysplasia</title><source>MEDLINE</source><source>Baishideng "World Journal of" online journals</source><source>EZB-FREE-00999 freely available EZB journals</source><source>PubMed Central</source><source>Alma/SFX Local Collection</source><creator>Fujita, Mikiko ; Nakamura, Yuri ; Kasashima, Saeko ; Furukawa, Maiko ; Misaka, Ryoichi ; Nagahara, Hikaru</creator><creatorcontrib>Fujita, Mikiko ; Nakamura, Yuri ; Kasashima, Saeko ; Furukawa, Maiko ; Misaka, Ryoichi ; Nagahara, Hikaru</creatorcontrib><description>AIM:To elucidate risk factors associated with dysplasia of short-segment Barrett’s esophagus(BE).METHODS:A total of 151 BE patients who underwent endoscopic examination from 2004 to 2008 in Aoyama Hospital,Tokyo Women’s Medical University,Japan and whose diagnosis was confirmed from biopsy specimens were enrolled in the study.BE was diagnosed based on endoscopic findings of gastric-appearing mucosa or apparent columnar-lined esophagus proximal to the esophagogastric junction.Dysplasia was classified into three grades-mild,moderate and severe-according to the guidelines of the Vienna Classification System for gastrointestinal epithelial neoplasia.Anthropometric and biochemical data were analyzed to identify risk factors for BE dysplasia.The prevalence of Helicobacter pylori(H.pylori)infection and the expression of p53 by immunohistological staining were also investigated.RESULTS:Histological examination classified patients into three types:specialized columnar epithelium(SCE)(n=65);junctional(n=38);and gastric fundic(n =48).The incidence of dysplasia or adenocarcinoma from BE of the SCE type was significantly higher than that of the other two types(P&lt;0.01).The univariate analysis revealed that sex,H.pylori infection,body weight,p53 overexpression,and low diastolic blood pressure(BP)were associated with BE dysplasia.In contrast,body mass index,waist circumference,metabolic syndrome complications,and variables related to glucose or lipid metabolism were not associated with dysplasia.Multivariate logistic analysis showed that overexpression of p53[odds ratio(OR)=13.1,P=0.004],H.pylori infection(OR=0.19,P=0.066),and diastolic BP(OR=0.87,P=0.021)were independent risk factors for epithelial dysplasia in BE patients with the SCE type.CONCLUSION:Overexpression of p53 is a risk factor for dysplasia of BE,however,H.pylori infection and diastolic BP inversely associated with BE dysplasia might be protective.</description><identifier>ISSN: 1007-9327</identifier><identifier>EISSN: 2219-2840</identifier><identifier>DOI: 10.3748/wjg.v20.i15.4353</identifier><identifier>PMID: 24764673</identifier><language>eng</language><publisher>United States: Baishideng Publishing Group Co., Limited</publisher><subject>Aged ; Anthropometry ; Barrett Esophagus - complications ; Barrett Esophagus - pathology ; Barrett’s ; Biopsy ; Blood Pressure ; Body Mass Index ; Body Weight ; dysplasia ; Endoscopy ; Esophageal Diseases - complications ; Esophageal Diseases - pathology ; esophagus ; Female ; Gastric Mucosa - pathology ; Helicobacter ; Helicobacter Infections - complications ; Humans ; Japan ; Lipid Metabolism ; Male ; Metabolic Syndrome - complications ; Middle Aged ; Odds Ratio ; Prevalence ; pylori ; Research Report ; Risk Factors ; Tumor Suppressor Protein p53 - metabolism</subject><ispartof>World journal of gastroenterology : WJG, 2014-04, Vol.20 (15), p.4353-4361</ispartof><rights>2014 Baishideng Publishing Group Co., Limited. All rights reserved. 2014</rights><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c440t-1cc3380a74fbd01f556ea65bbc423587243236094b31810c3373acb5afadccb13</citedby></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Uhttp://image.cqvip.com/vip1000/qk/84123X/84123X.jpg</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989971/pdf/$$EPDF$$P50$$Gpubmedcentral$$H</linktopdf><linktohtml>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC3989971/$$EHTML$$P50$$Gpubmedcentral$$H</linktohtml><link.rule.ids>230,314,727,780,784,885,27924,27925,53791,53793</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/24764673$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Fujita, Mikiko</creatorcontrib><creatorcontrib>Nakamura, Yuri</creatorcontrib><creatorcontrib>Kasashima, Saeko</creatorcontrib><creatorcontrib>Furukawa, Maiko</creatorcontrib><creatorcontrib>Misaka, Ryoichi</creatorcontrib><creatorcontrib>Nagahara, Hikaru</creatorcontrib><title>Risk factors associated with Barrett’s epithelial dysplasia</title><title>World journal of gastroenterology : WJG</title><addtitle>World Journal of Gastroenterology</addtitle><description>AIM:To elucidate risk factors associated with dysplasia of short-segment Barrett’s esophagus(BE).METHODS:A total of 151 BE patients who underwent endoscopic examination from 2004 to 2008 in Aoyama Hospital,Tokyo Women’s Medical University,Japan and whose diagnosis was confirmed from biopsy specimens were enrolled in the study.BE was diagnosed based on endoscopic findings of gastric-appearing mucosa or apparent columnar-lined esophagus proximal to the esophagogastric junction.Dysplasia was classified into three grades-mild,moderate and severe-according to the guidelines of the Vienna Classification System for gastrointestinal epithelial neoplasia.Anthropometric and biochemical data were analyzed to identify risk factors for BE dysplasia.The prevalence of Helicobacter pylori(H.pylori)infection and the expression of p53 by immunohistological staining were also investigated.RESULTS:Histological examination classified patients into three types:specialized columnar epithelium(SCE)(n=65);junctional(n=38);and gastric fundic(n =48).The incidence of dysplasia or adenocarcinoma from BE of the SCE type was significantly higher than that of the other two types(P&lt;0.01).The univariate analysis revealed that sex,H.pylori infection,body weight,p53 overexpression,and low diastolic blood pressure(BP)were associated with BE dysplasia.In contrast,body mass index,waist circumference,metabolic syndrome complications,and variables related to glucose or lipid metabolism were not associated with dysplasia.Multivariate logistic analysis showed that overexpression of p53[odds ratio(OR)=13.1,P=0.004],H.pylori infection(OR=0.19,P=0.066),and diastolic BP(OR=0.87,P=0.021)were independent risk factors for epithelial dysplasia in BE patients with the SCE type.CONCLUSION:Overexpression of p53 is a risk factor for dysplasia of BE,however,H.pylori infection and diastolic BP inversely associated with BE dysplasia might be protective.</description><subject>Aged</subject><subject>Anthropometry</subject><subject>Barrett Esophagus - complications</subject><subject>Barrett Esophagus - pathology</subject><subject>Barrett’s</subject><subject>Biopsy</subject><subject>Blood Pressure</subject><subject>Body Mass Index</subject><subject>Body Weight</subject><subject>dysplasia</subject><subject>Endoscopy</subject><subject>Esophageal Diseases - complications</subject><subject>Esophageal Diseases - pathology</subject><subject>esophagus</subject><subject>Female</subject><subject>Gastric Mucosa - pathology</subject><subject>Helicobacter</subject><subject>Helicobacter Infections - complications</subject><subject>Humans</subject><subject>Japan</subject><subject>Lipid Metabolism</subject><subject>Male</subject><subject>Metabolic Syndrome - complications</subject><subject>Middle Aged</subject><subject>Odds Ratio</subject><subject>Prevalence</subject><subject>pylori</subject><subject>Research Report</subject><subject>Risk Factors</subject><subject>Tumor Suppressor Protein p53 - metabolism</subject><issn>1007-9327</issn><issn>2219-2840</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2014</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNpVkM9q3DAQh0VpabZp7z0VH3vxdqSRLOnQQhv6DwKBkJ7FWJZ3lXrtjeRNyK2v0dfrk0RLtksrGASab34jPsZec1iilubd3fVqeStgGblaSlT4hC2E4LYWRsJTtuAAurYo9Al7kfM1gEBU4jk7EVI3stG4YO8vY_5Z9eTnKeWKcp58pDl01V2c19UnSinM859fv3MVtuUlDJGGqrvP24FypJfsWU9DDq8O9yn78eXz1dm3-vzi6_ezj-e1lxLmmnuPaIC07NsOeK9UE6hRbeulQGW0kCiwAStb5IZDgTWSbxX11HnfcjxlHx5zt7t2EzofxjnR4LYpbijdu4mi-78zxrVbTbcOrbFW7wPeHgLSdLMLeXabmH0YBhrDtMuOK25Fg9DYgsIj6tOUcwr9cQ0Ht7fuinVXrLti3e2tl5E3_37vOPBXcwHwkLmextVNHFdHxoLZH6tAGmmVKIXSKCixDyF5kBs</recordid><startdate>20140421</startdate><enddate>20140421</enddate><creator>Fujita, Mikiko</creator><creator>Nakamura, Yuri</creator><creator>Kasashima, Saeko</creator><creator>Furukawa, Maiko</creator><creator>Misaka, Ryoichi</creator><creator>Nagahara, Hikaru</creator><general>Baishideng Publishing Group Co., Limited</general><scope>2RA</scope><scope>92L</scope><scope>CQIGP</scope><scope>W91</scope><scope>~WA</scope><scope>CGR</scope><scope>CUY</scope><scope>CVF</scope><scope>ECM</scope><scope>EIF</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>7X8</scope><scope>5PM</scope></search><sort><creationdate>20140421</creationdate><title>Risk factors associated with Barrett’s epithelial dysplasia</title><author>Fujita, Mikiko ; Nakamura, Yuri ; Kasashima, Saeko ; Furukawa, Maiko ; Misaka, Ryoichi ; Nagahara, Hikaru</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c440t-1cc3380a74fbd01f556ea65bbc423587243236094b31810c3373acb5afadccb13</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2014</creationdate><topic>Aged</topic><topic>Anthropometry</topic><topic>Barrett Esophagus - complications</topic><topic>Barrett Esophagus - pathology</topic><topic>Barrett’s</topic><topic>Biopsy</topic><topic>Blood Pressure</topic><topic>Body Mass Index</topic><topic>Body Weight</topic><topic>dysplasia</topic><topic>Endoscopy</topic><topic>Esophageal Diseases - complications</topic><topic>Esophageal Diseases - pathology</topic><topic>esophagus</topic><topic>Female</topic><topic>Gastric Mucosa - pathology</topic><topic>Helicobacter</topic><topic>Helicobacter Infections - complications</topic><topic>Humans</topic><topic>Japan</topic><topic>Lipid Metabolism</topic><topic>Male</topic><topic>Metabolic Syndrome - complications</topic><topic>Middle Aged</topic><topic>Odds Ratio</topic><topic>Prevalence</topic><topic>pylori</topic><topic>Research Report</topic><topic>Risk Factors</topic><topic>Tumor Suppressor Protein p53 - metabolism</topic><toplevel>online_resources</toplevel><creatorcontrib>Fujita, Mikiko</creatorcontrib><creatorcontrib>Nakamura, Yuri</creatorcontrib><creatorcontrib>Kasashima, Saeko</creatorcontrib><creatorcontrib>Furukawa, Maiko</creatorcontrib><creatorcontrib>Misaka, Ryoichi</creatorcontrib><creatorcontrib>Nagahara, Hikaru</creatorcontrib><collection>中文科技期刊数据库</collection><collection>中文科技期刊数据库-CALIS站点</collection><collection>中文科技期刊数据库-7.0平台</collection><collection>中文科技期刊数据库-医药卫生</collection><collection>中文科技期刊数据库- 镜像站点</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>World journal of gastroenterology : WJG</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Fujita, Mikiko</au><au>Nakamura, Yuri</au><au>Kasashima, Saeko</au><au>Furukawa, Maiko</au><au>Misaka, Ryoichi</au><au>Nagahara, Hikaru</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Risk factors associated with Barrett’s epithelial dysplasia</atitle><jtitle>World journal of gastroenterology : WJG</jtitle><addtitle>World Journal of Gastroenterology</addtitle><date>2014-04-21</date><risdate>2014</risdate><volume>20</volume><issue>15</issue><spage>4353</spage><epage>4361</epage><pages>4353-4361</pages><issn>1007-9327</issn><eissn>2219-2840</eissn><abstract>AIM:To elucidate risk factors associated with dysplasia of short-segment Barrett’s esophagus(BE).METHODS:A total of 151 BE patients who underwent endoscopic examination from 2004 to 2008 in Aoyama Hospital,Tokyo Women’s Medical University,Japan and whose diagnosis was confirmed from biopsy specimens were enrolled in the study.BE was diagnosed based on endoscopic findings of gastric-appearing mucosa or apparent columnar-lined esophagus proximal to the esophagogastric junction.Dysplasia was classified into three grades-mild,moderate and severe-according to the guidelines of the Vienna Classification System for gastrointestinal epithelial neoplasia.Anthropometric and biochemical data were analyzed to identify risk factors for BE dysplasia.The prevalence of Helicobacter pylori(H.pylori)infection and the expression of p53 by immunohistological staining were also investigated.RESULTS:Histological examination classified patients into three types:specialized columnar epithelium(SCE)(n=65);junctional(n=38);and gastric fundic(n =48).The incidence of dysplasia or adenocarcinoma from BE of the SCE type was significantly higher than that of the other two types(P&lt;0.01).The univariate analysis revealed that sex,H.pylori infection,body weight,p53 overexpression,and low diastolic blood pressure(BP)were associated with BE dysplasia.In contrast,body mass index,waist circumference,metabolic syndrome complications,and variables related to glucose or lipid metabolism were not associated with dysplasia.Multivariate logistic analysis showed that overexpression of p53[odds ratio(OR)=13.1,P=0.004],H.pylori infection(OR=0.19,P=0.066),and diastolic BP(OR=0.87,P=0.021)were independent risk factors for epithelial dysplasia in BE patients with the SCE type.CONCLUSION:Overexpression of p53 is a risk factor for dysplasia of BE,however,H.pylori infection and diastolic BP inversely associated with BE dysplasia might be protective.</abstract><cop>United States</cop><pub>Baishideng Publishing Group Co., Limited</pub><pmid>24764673</pmid><doi>10.3748/wjg.v20.i15.4353</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record> |
fulltext | fulltext |
identifier | ISSN: 1007-9327 |
ispartof | World journal of gastroenterology : WJG, 2014-04, Vol.20 (15), p.4353-4361 |
issn | 1007-9327 2219-2840 |
language | eng |
recordid | cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_3989971 |
source | MEDLINE; Baishideng "World Journal of" online journals; EZB-FREE-00999 freely available EZB journals; PubMed Central; Alma/SFX Local Collection |
subjects | Aged Anthropometry Barrett Esophagus - complications Barrett Esophagus - pathology Barrett’s Biopsy Blood Pressure Body Mass Index Body Weight dysplasia Endoscopy Esophageal Diseases - complications Esophageal Diseases - pathology esophagus Female Gastric Mucosa - pathology Helicobacter Helicobacter Infections - complications Humans Japan Lipid Metabolism Male Metabolic Syndrome - complications Middle Aged Odds Ratio Prevalence pylori Research Report Risk Factors Tumor Suppressor Protein p53 - metabolism |
title | Risk factors associated with Barrett’s epithelial dysplasia |
url | https://sfx.bib-bvb.de/sfx_tum?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-01T15%3A32%3A24IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-proquest_pubme&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Risk%20factors%20associated%20with%20Barrett%E2%80%99s%20epithelial%20dysplasia&rft.jtitle=World%20journal%20of%20gastroenterology%20:%20WJG&rft.au=Fujita,%20Mikiko&rft.date=2014-04-21&rft.volume=20&rft.issue=15&rft.spage=4353&rft.epage=4361&rft.pages=4353-4361&rft.issn=1007-9327&rft.eissn=2219-2840&rft_id=info:doi/10.3748/wjg.v20.i15.4353&rft_dat=%3Cproquest_pubme%3E1519263069%3C/proquest_pubme%3E%3Curl%3E%3C/url%3E&disable_directlink=true&sfx.directlink=off&sfx.report_link=0&rft_id=info:oai/&rft_pqid=1519263069&rft_id=info:pmid/24764673&rft_cqvip_id=90888889504849524953485053&rfr_iscdi=true |