First-degree relatives of patients with early-onset gastric carcinoma show even at young ages a high prevalence of advanced OLGA/OLGIM stages and dysplasia

Summary Background First‐degree relatives (FDRs) of early‐onset gastric carcinoma (EOGC) patients are at increased risk of cancer development. OLGA/OLGIM (Operative Link on Gastritis/Intestinal Metaplasia Assessment) classifications have been proposed for the identification of individuals at high ri...

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Veröffentlicht in:Alimentary pharmacology & therapeutics 2012-06, Vol.35 (12), p.1451-1459
Hauptverfasser: Marcos-Pinto, R., Carneiro, F., Dinis-Ribeiro, M., Wen, X., Lopes, C., Figueiredo, C., Machado, J. C., Ferreira, R. M., Reis, C. A., Ferreira, J., Pedroto, I., Areias, J.
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container_issue 12
container_start_page 1451
container_title Alimentary pharmacology & therapeutics
container_volume 35
creator Marcos-Pinto, R.
Carneiro, F.
Dinis-Ribeiro, M.
Wen, X.
Lopes, C.
Figueiredo, C.
Machado, J. C.
Ferreira, R. M.
Reis, C. A.
Ferreira, J.
Pedroto, I.
Areias, J.
description Summary Background First‐degree relatives (FDRs) of early‐onset gastric carcinoma (EOGC) patients are at increased risk of cancer development. OLGA/OLGIM (Operative Link on Gastritis/Intestinal Metaplasia Assessment) classifications have been proposed for the identification of individuals at high risk of gastric cancer development. Aim To estimate the prevalence and severity of premalignant conditions and lesions in FDRs of EOGC patients. Methods A case–control study was conducted encompassing 103 FDRs of EOGC patients (cases) and 101 age‐ and gender‐matched controls, all submitted to upper GI endoscopy and OLGA and OLGIM used for staging as well as modified versions with exclusion of the biopsies from incisura angularis in the analysis. Results Helicobacter pylori infection was present in 82% of cases (P = 0.001). Atrophy was present in 70% of cases (OLGA stages I–IV). High‐risk stages (III–IV) were identified only in cases (19%) (P 
doi_str_mv 10.1111/j.1365-2036.2012.05111.x
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C. ; Ferreira, R. M. ; Reis, C. A. ; Ferreira, J. ; Pedroto, I. ; Areias, J.</creator><creatorcontrib>Marcos-Pinto, R. ; Carneiro, F. ; Dinis-Ribeiro, M. ; Wen, X. ; Lopes, C. ; Figueiredo, C. ; Machado, J. C. ; Ferreira, R. M. ; Reis, C. A. ; Ferreira, J. ; Pedroto, I. ; Areias, J.</creatorcontrib><description>Summary Background First‐degree relatives (FDRs) of early‐onset gastric carcinoma (EOGC) patients are at increased risk of cancer development. OLGA/OLGIM (Operative Link on Gastritis/Intestinal Metaplasia Assessment) classifications have been proposed for the identification of individuals at high risk of gastric cancer development. Aim To estimate the prevalence and severity of premalignant conditions and lesions in FDRs of EOGC patients. Methods A case–control study was conducted encompassing 103 FDRs of EOGC patients (cases) and 101 age‐ and gender‐matched controls, all submitted to upper GI endoscopy and OLGA and OLGIM used for staging as well as modified versions with exclusion of the biopsies from incisura angularis in the analysis. Results Helicobacter pylori infection was present in 82% of cases (P = 0.001). Atrophy was present in 70% of cases (OLGA stages I–IV). High‐risk stages (III–IV) were identified only in cases (19%) (P &lt; 0.001). Dysplasia was diagnosed only in cases (n = 7, P = 0.007). The application of OLGIM, modified OLGA and modified OLGIM classifications led to downgrade of stages in comparison with the original OLGA classification (27%, 15% and 30% respectively). In all classification systems, dysplastic lesions clustered (86%) in high‐risk stages. Conclusions FDRs of EOGC patients have, even at young ages, a high prevalence of H. pylori infection, high‐risk OLGA and OLGIM stages and dysplasia. These patients should undergo accurate endoscopic observation with at least four biopsies in antrum and corpus to allow adequate staging and follow‐up of premalignant conditions and lesions scored in high‐risk stages, in accordance with international guidelines recently proposed.</description><identifier>ISSN: 0269-2813</identifier><identifier>EISSN: 1365-2036</identifier><identifier>DOI: 10.1111/j.1365-2036.2012.05111.x</identifier><identifier>PMID: 22548492</identifier><language>eng</language><publisher>Oxford: Blackwell Publishing Ltd</publisher><subject>Adult ; Age Factors ; Biological and medical sciences ; Case-Control Studies ; Digestive system ; Endoscopy, Gastrointestinal - methods ; Female ; Gastritis - microbiology ; Gastritis - pathology ; Gastroenterology. Liver. Pancreas. Abdomen ; Helicobacter Infections - pathology ; Helicobacter pylori - isolation &amp; purification ; Humans ; Male ; Medical sciences ; Metaplasia - pathology ; Pedigree ; Pharmacology. Drug treatments ; Precancerous Conditions - chemically induced ; Precancerous Conditions - pathology ; Risk Factors ; Severity of Illness Index ; Statistics as Topic ; Stomach - pathology ; Stomach Neoplasms - pathology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Time Factors ; Tumors</subject><ispartof>Alimentary pharmacology &amp; therapeutics, 2012-06, Vol.35 (12), p.1451-1459</ispartof><rights>2012 Blackwell Publishing Ltd</rights><rights>2015 INIST-CNRS</rights><rights>2012 Blackwell Publishing Ltd.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4871-4560c132622c18cc45785fedbf0f76cbe67885321acb7b9e7aa303cc87ebb5723</citedby><cites>FETCH-LOGICAL-c4871-4560c132622c18cc45785fedbf0f76cbe67885321acb7b9e7aa303cc87ebb5723</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1111%2Fj.1365-2036.2012.05111.x$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1111%2Fj.1365-2036.2012.05111.x$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,780,784,1417,1433,27924,27925,45574,45575,46409,46833</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=25911683$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22548492$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Marcos-Pinto, R.</creatorcontrib><creatorcontrib>Carneiro, F.</creatorcontrib><creatorcontrib>Dinis-Ribeiro, M.</creatorcontrib><creatorcontrib>Wen, X.</creatorcontrib><creatorcontrib>Lopes, C.</creatorcontrib><creatorcontrib>Figueiredo, C.</creatorcontrib><creatorcontrib>Machado, J. C.</creatorcontrib><creatorcontrib>Ferreira, R. M.</creatorcontrib><creatorcontrib>Reis, C. A.</creatorcontrib><creatorcontrib>Ferreira, J.</creatorcontrib><creatorcontrib>Pedroto, I.</creatorcontrib><creatorcontrib>Areias, J.</creatorcontrib><title>First-degree relatives of patients with early-onset gastric carcinoma show even at young ages a high prevalence of advanced OLGA/OLGIM stages and dysplasia</title><title>Alimentary pharmacology &amp; therapeutics</title><addtitle>Aliment Pharmacol Ther</addtitle><description>Summary Background First‐degree relatives (FDRs) of early‐onset gastric carcinoma (EOGC) patients are at increased risk of cancer development. OLGA/OLGIM (Operative Link on Gastritis/Intestinal Metaplasia Assessment) classifications have been proposed for the identification of individuals at high risk of gastric cancer development. Aim To estimate the prevalence and severity of premalignant conditions and lesions in FDRs of EOGC patients. Methods A case–control study was conducted encompassing 103 FDRs of EOGC patients (cases) and 101 age‐ and gender‐matched controls, all submitted to upper GI endoscopy and OLGA and OLGIM used for staging as well as modified versions with exclusion of the biopsies from incisura angularis in the analysis. Results Helicobacter pylori infection was present in 82% of cases (P = 0.001). Atrophy was present in 70% of cases (OLGA stages I–IV). High‐risk stages (III–IV) were identified only in cases (19%) (P &lt; 0.001). Dysplasia was diagnosed only in cases (n = 7, P = 0.007). The application of OLGIM, modified OLGA and modified OLGIM classifications led to downgrade of stages in comparison with the original OLGA classification (27%, 15% and 30% respectively). In all classification systems, dysplastic lesions clustered (86%) in high‐risk stages. Conclusions FDRs of EOGC patients have, even at young ages, a high prevalence of H. pylori infection, high‐risk OLGA and OLGIM stages and dysplasia. These patients should undergo accurate endoscopic observation with at least four biopsies in antrum and corpus to allow adequate staging and follow‐up of premalignant conditions and lesions scored in high‐risk stages, in accordance with international guidelines recently proposed.</description><subject>Adult</subject><subject>Age Factors</subject><subject>Biological and medical sciences</subject><subject>Case-Control Studies</subject><subject>Digestive system</subject><subject>Endoscopy, Gastrointestinal - methods</subject><subject>Female</subject><subject>Gastritis - microbiology</subject><subject>Gastritis - pathology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Helicobacter Infections - pathology</subject><subject>Helicobacter pylori - isolation &amp; purification</subject><subject>Humans</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Metaplasia - pathology</subject><subject>Pedigree</subject><subject>Pharmacology. Drug treatments</subject><subject>Precancerous Conditions - chemically induced</subject><subject>Precancerous Conditions - pathology</subject><subject>Risk Factors</subject><subject>Severity of Illness Index</subject><subject>Statistics as Topic</subject><subject>Stomach - pathology</subject><subject>Stomach Neoplasms - pathology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. 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C.</creator><creator>Ferreira, R. M.</creator><creator>Reis, C. A.</creator><creator>Ferreira, J.</creator><creator>Pedroto, I.</creator><creator>Areias, J.</creator><general>Blackwell Publishing Ltd</general><general>Blackwell</general><scope>BSCLL</scope><scope>IQODW</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></search><sort><creationdate>201206</creationdate><title>First-degree relatives of patients with early-onset gastric carcinoma show even at young ages a high prevalence of advanced OLGA/OLGIM stages and dysplasia</title><author>Marcos-Pinto, R. ; Carneiro, F. ; Dinis-Ribeiro, M. ; Wen, X. ; Lopes, C. ; Figueiredo, C. ; Machado, J. C. ; Ferreira, R. M. ; Reis, C. 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Drug treatments</topic><topic>Precancerous Conditions - chemically induced</topic><topic>Precancerous Conditions - pathology</topic><topic>Risk Factors</topic><topic>Severity of Illness Index</topic><topic>Statistics as Topic</topic><topic>Stomach - pathology</topic><topic>Stomach Neoplasms - pathology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Time Factors</topic><topic>Tumors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Marcos-Pinto, R.</creatorcontrib><creatorcontrib>Carneiro, F.</creatorcontrib><creatorcontrib>Dinis-Ribeiro, M.</creatorcontrib><creatorcontrib>Wen, X.</creatorcontrib><creatorcontrib>Lopes, C.</creatorcontrib><creatorcontrib>Figueiredo, C.</creatorcontrib><creatorcontrib>Machado, J. C.</creatorcontrib><creatorcontrib>Ferreira, R. M.</creatorcontrib><creatorcontrib>Reis, C. A.</creatorcontrib><creatorcontrib>Ferreira, J.</creatorcontrib><creatorcontrib>Pedroto, I.</creatorcontrib><creatorcontrib>Areias, J.</creatorcontrib><collection>Istex</collection><collection>Pascal-Francis</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><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Marcos-Pinto, R.</au><au>Carneiro, F.</au><au>Dinis-Ribeiro, M.</au><au>Wen, X.</au><au>Lopes, C.</au><au>Figueiredo, C.</au><au>Machado, J. C.</au><au>Ferreira, R. M.</au><au>Reis, C. A.</au><au>Ferreira, J.</au><au>Pedroto, I.</au><au>Areias, J.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>First-degree relatives of patients with early-onset gastric carcinoma show even at young ages a high prevalence of advanced OLGA/OLGIM stages and dysplasia</atitle><jtitle>Alimentary pharmacology &amp; therapeutics</jtitle><addtitle>Aliment Pharmacol Ther</addtitle><date>2012-06</date><risdate>2012</risdate><volume>35</volume><issue>12</issue><spage>1451</spage><epage>1459</epage><pages>1451-1459</pages><issn>0269-2813</issn><eissn>1365-2036</eissn><abstract>Summary Background First‐degree relatives (FDRs) of early‐onset gastric carcinoma (EOGC) patients are at increased risk of cancer development. OLGA/OLGIM (Operative Link on Gastritis/Intestinal Metaplasia Assessment) classifications have been proposed for the identification of individuals at high risk of gastric cancer development. Aim To estimate the prevalence and severity of premalignant conditions and lesions in FDRs of EOGC patients. Methods A case–control study was conducted encompassing 103 FDRs of EOGC patients (cases) and 101 age‐ and gender‐matched controls, all submitted to upper GI endoscopy and OLGA and OLGIM used for staging as well as modified versions with exclusion of the biopsies from incisura angularis in the analysis. Results Helicobacter pylori infection was present in 82% of cases (P = 0.001). Atrophy was present in 70% of cases (OLGA stages I–IV). High‐risk stages (III–IV) were identified only in cases (19%) (P &lt; 0.001). Dysplasia was diagnosed only in cases (n = 7, P = 0.007). The application of OLGIM, modified OLGA and modified OLGIM classifications led to downgrade of stages in comparison with the original OLGA classification (27%, 15% and 30% respectively). In all classification systems, dysplastic lesions clustered (86%) in high‐risk stages. Conclusions FDRs of EOGC patients have, even at young ages, a high prevalence of H. pylori infection, high‐risk OLGA and OLGIM stages and dysplasia. These patients should undergo accurate endoscopic observation with at least four biopsies in antrum and corpus to allow adequate staging and follow‐up of premalignant conditions and lesions scored in high‐risk stages, in accordance with international guidelines recently proposed.</abstract><cop>Oxford</cop><pub>Blackwell Publishing Ltd</pub><pmid>22548492</pmid><doi>10.1111/j.1365-2036.2012.05111.x</doi><tpages>9</tpages><oa>free_for_read</oa></addata></record>
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subjects Adult
Age Factors
Biological and medical sciences
Case-Control Studies
Digestive system
Endoscopy, Gastrointestinal - methods
Female
Gastritis - microbiology
Gastritis - pathology
Gastroenterology. Liver. Pancreas. Abdomen
Helicobacter Infections - pathology
Helicobacter pylori - isolation & purification
Humans
Male
Medical sciences
Metaplasia - pathology
Pedigree
Pharmacology. Drug treatments
Precancerous Conditions - chemically induced
Precancerous Conditions - pathology
Risk Factors
Severity of Illness Index
Statistics as Topic
Stomach - pathology
Stomach Neoplasms - pathology
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Time Factors
Tumors
title First-degree relatives of patients with early-onset gastric carcinoma show even at young ages a high prevalence of advanced OLGA/OLGIM stages and dysplasia
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