Prevalence of Extensive and Limited Gastric Intestinal Metaplasia and Progression to Dysplasia and Gastric Cancer
Background and Aims Guidelines cite extensive gastric intestinal metaplasia (GIM) as a bigger risk factor for gastric cancer (GC) than limited GIM and an indication for endoscopic surveillance. Data on progression of extensive GIM to GC in the USA are limited. This study aimed to estimate the preval...
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description | Background and Aims
Guidelines cite extensive gastric intestinal metaplasia (GIM) as a bigger risk factor for gastric cancer (GC) than limited GIM and an indication for endoscopic surveillance. Data on progression of extensive GIM to GC in the USA are limited. This study aimed to estimate the prevalence and progression rates of extensive GIM in a US cohort.
Methods
This retrospective study assessed the prevalence of extensive GIM between 1/1/1990 and 8/1/2019 at a large academic medical center. Multivariable regression was used to identify predictors of extensive GIM. Incidence of GC on follow-up was calculated as number of new diagnoses divided by person-years of follow-up. Presence of GIM on subsequent follow-up endoscopy was assessed.
Results
Of 1256 individuals with GIM, 352 (28%) had extensive GIM and 904 (72%) had limited GIM. On multivariable analysis, older age (OR 1.01, 95% CI 1.00–1.02) and Hispanic ethnicity (OR 1.55, 95% CI 1.11–2.16) were predictive of extensive GIM. The annual incidence of GC for GIM overall was 0.09%. There was no difference in progression to GC between extensive or limited GIM (IRR 0, 95% CI 0–2.6), or to advanced lesions overall (IRR 0.37, 95% CI 0.04–1.62). 70% of individuals had persistent GIM on follow-up biopsy, and 22% with limited GIM had extensive GIM on follow-up biopsy.
Conclusions
28% of individuals with GIM have the extensive subtype, and are more likely to be older and of Hispanic ethnicity. There was no difference in progression to GC between extensive and limited GIM. Further research is needed to better assess risk of GIM in the US context. |
doi_str_mv | 10.1007/s10620-021-07276-9 |
format | Article |
fullrecord | <record><control><sourceid>gale_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_9013391</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A710409161</galeid><sourcerecordid>A710409161</sourcerecordid><originalsourceid>FETCH-LOGICAL-c607t-b3b72781b624f82d042a3bac506e528cd26ba78ad603faabbdc34b01925783123</originalsourceid><addsrcrecordid>eNp9kk1v1DAQhi0EotvCH-CAInHhkjK2E39ckKqlLZUW0QOcLceZLK6y9tbOrui_x9vtJ0LIh1ieZ97JO3oJeUfhmALIT5mCYFADozVIJkWtX5AZbSWvWSvUSzIDKsqdUnFADnO-AgAtqXhNDngjWkk1m5Hry4RbO2JwWMWhOv09Ych-i5UNfbXwKz9hX53bPCXvqoswYZ58sGP1DSe7Hm329pa8THGZMGcfQzXF6stNflK8b5_bMiW9Ia8GO2Z8e_c9Ij_PTn_Mv9aL7-cX85NF7QTIqe54Vzwp2gnWDIr10DDLO-taENgy5XomOiuV7QXwwdqu6x1vOiimWqk4ZfyIfN7rrjfdCnuHYUp2NOvkVzbdmGi9eV4J_pdZxq3RQDnXtAh8vBNI8XpTjJuVzw7H0QaMm2xYqzinkmlV0A9_oVdxk8qeCiWU1kqKRj9Sy7Jw48MQy1y3EzUnkkIDmord2ON_UOX0uPIuBhx8eX_WwPYNLsWcEw4PHimYXVDMPiimBMXcBsXs_uX90-08tNwnowB8D-RSCktMj5b-I_sHZprInQ</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2689987649</pqid></control><display><type>article</type><title>Prevalence of Extensive and Limited Gastric Intestinal Metaplasia and Progression to Dysplasia and Gastric Cancer</title><source>MEDLINE</source><source>SpringerNature Journals</source><creator>Laszkowska, Monika ; Truong, Han ; Faye, Adam S. ; Kim, Judith ; Tan, Sarah Xinhui ; Lim, Francesca ; Abrams, Julian A. ; Hur, Chin</creator><creatorcontrib>Laszkowska, Monika ; Truong, Han ; Faye, Adam S. ; Kim, Judith ; Tan, Sarah Xinhui ; Lim, Francesca ; Abrams, Julian A. ; Hur, Chin</creatorcontrib><description>Background and Aims
Guidelines cite extensive gastric intestinal metaplasia (GIM) as a bigger risk factor for gastric cancer (GC) than limited GIM and an indication for endoscopic surveillance. Data on progression of extensive GIM to GC in the USA are limited. This study aimed to estimate the prevalence and progression rates of extensive GIM in a US cohort.
Methods
This retrospective study assessed the prevalence of extensive GIM between 1/1/1990 and 8/1/2019 at a large academic medical center. Multivariable regression was used to identify predictors of extensive GIM. Incidence of GC on follow-up was calculated as number of new diagnoses divided by person-years of follow-up. Presence of GIM on subsequent follow-up endoscopy was assessed.
Results
Of 1256 individuals with GIM, 352 (28%) had extensive GIM and 904 (72%) had limited GIM. On multivariable analysis, older age (OR 1.01, 95% CI 1.00–1.02) and Hispanic ethnicity (OR 1.55, 95% CI 1.11–2.16) were predictive of extensive GIM. The annual incidence of GC for GIM overall was 0.09%. There was no difference in progression to GC between extensive or limited GIM (IRR 0, 95% CI 0–2.6), or to advanced lesions overall (IRR 0.37, 95% CI 0.04–1.62). 70% of individuals had persistent GIM on follow-up biopsy, and 22% with limited GIM had extensive GIM on follow-up biopsy.
Conclusions
28% of individuals with GIM have the extensive subtype, and are more likely to be older and of Hispanic ethnicity. There was no difference in progression to GC between extensive and limited GIM. Further research is needed to better assess risk of GIM in the US context.</description><identifier>ISSN: 0163-2116</identifier><identifier>EISSN: 1573-2568</identifier><identifier>DOI: 10.1007/s10620-021-07276-9</identifier><identifier>PMID: 34657192</identifier><language>eng</language><publisher>New York: Springer US</publisher><subject>Analysis ; Biochemistry ; Biopsy ; Cancer ; Development and progression ; Dysplasia ; Endoscopy ; Endoscopy, Gastrointestinal ; Ethnicity ; Gastric cancer ; Gastroenterology ; Health aspects ; Hepatology ; Humans ; Hyperplasia ; Medical centers ; Medical colleges ; Medicine ; Medicine & Public Health ; Metaplasia - epidemiology ; Oncology ; Original Article ; Precancerous Conditions - pathology ; Prevalence ; Retrospective Studies ; Stomach cancer ; Stomach Neoplasms - pathology ; Transplant Surgery</subject><ispartof>Digestive diseases and sciences, 2022-08, Vol.67 (8), p.3693-3701</ispartof><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021</rights><rights>2021. The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature.</rights><rights>COPYRIGHT 2022 Springer</rights><rights>The Author(s), under exclusive licence to Springer Science+Business Media, LLC, part of Springer Nature 2021.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c607t-b3b72781b624f82d042a3bac506e528cd26ba78ad603faabbdc34b01925783123</citedby><cites>FETCH-LOGICAL-c607t-b3b72781b624f82d042a3bac506e528cd26ba78ad603faabbdc34b01925783123</cites><orcidid>0000-0001-6816-3293</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://link.springer.com/content/pdf/10.1007/s10620-021-07276-9$$EPDF$$P50$$Gspringer$$H</linktopdf><linktohtml>$$Uhttps://link.springer.com/10.1007/s10620-021-07276-9$$EHTML$$P50$$Gspringer$$H</linktohtml><link.rule.ids>230,314,780,784,885,27924,27925,41488,42557,51319</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/34657192$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Laszkowska, Monika</creatorcontrib><creatorcontrib>Truong, Han</creatorcontrib><creatorcontrib>Faye, Adam S.</creatorcontrib><creatorcontrib>Kim, Judith</creatorcontrib><creatorcontrib>Tan, Sarah Xinhui</creatorcontrib><creatorcontrib>Lim, Francesca</creatorcontrib><creatorcontrib>Abrams, Julian A.</creatorcontrib><creatorcontrib>Hur, Chin</creatorcontrib><title>Prevalence of Extensive and Limited Gastric Intestinal Metaplasia and Progression to Dysplasia and Gastric Cancer</title><title>Digestive diseases and sciences</title><addtitle>Dig Dis Sci</addtitle><addtitle>Dig Dis Sci</addtitle><description>Background and Aims
Guidelines cite extensive gastric intestinal metaplasia (GIM) as a bigger risk factor for gastric cancer (GC) than limited GIM and an indication for endoscopic surveillance. Data on progression of extensive GIM to GC in the USA are limited. This study aimed to estimate the prevalence and progression rates of extensive GIM in a US cohort.
Methods
This retrospective study assessed the prevalence of extensive GIM between 1/1/1990 and 8/1/2019 at a large academic medical center. Multivariable regression was used to identify predictors of extensive GIM. Incidence of GC on follow-up was calculated as number of new diagnoses divided by person-years of follow-up. Presence of GIM on subsequent follow-up endoscopy was assessed.
Results
Of 1256 individuals with GIM, 352 (28%) had extensive GIM and 904 (72%) had limited GIM. On multivariable analysis, older age (OR 1.01, 95% CI 1.00–1.02) and Hispanic ethnicity (OR 1.55, 95% CI 1.11–2.16) were predictive of extensive GIM. The annual incidence of GC for GIM overall was 0.09%. There was no difference in progression to GC between extensive or limited GIM (IRR 0, 95% CI 0–2.6), or to advanced lesions overall (IRR 0.37, 95% CI 0.04–1.62). 70% of individuals had persistent GIM on follow-up biopsy, and 22% with limited GIM had extensive GIM on follow-up biopsy.
Conclusions
28% of individuals with GIM have the extensive subtype, and are more likely to be older and of Hispanic ethnicity. There was no difference in progression to GC between extensive and limited GIM. Further research is needed to better assess risk of GIM in the US context.</description><subject>Analysis</subject><subject>Biochemistry</subject><subject>Biopsy</subject><subject>Cancer</subject><subject>Development and progression</subject><subject>Dysplasia</subject><subject>Endoscopy</subject><subject>Endoscopy, Gastrointestinal</subject><subject>Ethnicity</subject><subject>Gastric cancer</subject><subject>Gastroenterology</subject><subject>Health aspects</subject><subject>Hepatology</subject><subject>Humans</subject><subject>Hyperplasia</subject><subject>Medical centers</subject><subject>Medical colleges</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Metaplasia - epidemiology</subject><subject>Oncology</subject><subject>Original Article</subject><subject>Precancerous Conditions - pathology</subject><subject>Prevalence</subject><subject>Retrospective Studies</subject><subject>Stomach cancer</subject><subject>Stomach Neoplasms - pathology</subject><subject>Transplant Surgery</subject><issn>0163-2116</issn><issn>1573-2568</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2022</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>AZQEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNp9kk1v1DAQhi0EotvCH-CAInHhkjK2E39ckKqlLZUW0QOcLceZLK6y9tbOrui_x9vtJ0LIh1ieZ97JO3oJeUfhmALIT5mCYFADozVIJkWtX5AZbSWvWSvUSzIDKsqdUnFADnO-AgAtqXhNDngjWkk1m5Hry4RbO2JwWMWhOv09Ych-i5UNfbXwKz9hX53bPCXvqoswYZ58sGP1DSe7Hm329pa8THGZMGcfQzXF6stNflK8b5_bMiW9Ia8GO2Z8e_c9Ij_PTn_Mv9aL7-cX85NF7QTIqe54Vzwp2gnWDIr10DDLO-taENgy5XomOiuV7QXwwdqu6x1vOiimWqk4ZfyIfN7rrjfdCnuHYUp2NOvkVzbdmGi9eV4J_pdZxq3RQDnXtAh8vBNI8XpTjJuVzw7H0QaMm2xYqzinkmlV0A9_oVdxk8qeCiWU1kqKRj9Sy7Jw48MQy1y3EzUnkkIDmord2ON_UOX0uPIuBhx8eX_WwPYNLsWcEw4PHimYXVDMPiimBMXcBsXs_uX90-08tNwnowB8D-RSCktMj5b-I_sHZprInQ</recordid><startdate>20220801</startdate><enddate>20220801</enddate><creator>Laszkowska, Monika</creator><creator>Truong, Han</creator><creator>Faye, Adam S.</creator><creator>Kim, Judith</creator><creator>Tan, Sarah Xinhui</creator><creator>Lim, Francesca</creator><creator>Abrams, Julian A.</creator><creator>Hur, Chin</creator><general>Springer US</general><general>Springer</general><general>Springer Nature B.V</general><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>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9-</scope><scope>K9.</scope><scope>KB0</scope><scope>M0R</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-6816-3293</orcidid></search><sort><creationdate>20220801</creationdate><title>Prevalence of Extensive and Limited Gastric Intestinal Metaplasia and Progression to Dysplasia and Gastric Cancer</title><author>Laszkowska, Monika ; Truong, Han ; Faye, Adam S. ; Kim, Judith ; Tan, Sarah Xinhui ; Lim, Francesca ; Abrams, Julian A. ; Hur, Chin</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c607t-b3b72781b624f82d042a3bac506e528cd26ba78ad603faabbdc34b01925783123</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Analysis</topic><topic>Biochemistry</topic><topic>Biopsy</topic><topic>Cancer</topic><topic>Development and progression</topic><topic>Dysplasia</topic><topic>Endoscopy</topic><topic>Endoscopy, Gastrointestinal</topic><topic>Ethnicity</topic><topic>Gastric cancer</topic><topic>Gastroenterology</topic><topic>Health aspects</topic><topic>Hepatology</topic><topic>Humans</topic><topic>Hyperplasia</topic><topic>Medical centers</topic><topic>Medical colleges</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Metaplasia - epidemiology</topic><topic>Oncology</topic><topic>Original Article</topic><topic>Precancerous Conditions - pathology</topic><topic>Prevalence</topic><topic>Retrospective Studies</topic><topic>Stomach cancer</topic><topic>Stomach Neoplasms - pathology</topic><topic>Transplant Surgery</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Laszkowska, Monika</creatorcontrib><creatorcontrib>Truong, Han</creatorcontrib><creatorcontrib>Faye, Adam S.</creatorcontrib><creatorcontrib>Kim, Judith</creatorcontrib><creatorcontrib>Tan, Sarah Xinhui</creatorcontrib><creatorcontrib>Lim, Francesca</creatorcontrib><creatorcontrib>Abrams, Julian A.</creatorcontrib><creatorcontrib>Hur, Chin</creatorcontrib><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>Consumer Health Database (Alumni Edition)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Consumer Health Database</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><jtitle>Digestive diseases and sciences</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Laszkowska, Monika</au><au>Truong, Han</au><au>Faye, Adam S.</au><au>Kim, Judith</au><au>Tan, Sarah Xinhui</au><au>Lim, Francesca</au><au>Abrams, Julian A.</au><au>Hur, Chin</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Prevalence of Extensive and Limited Gastric Intestinal Metaplasia and Progression to Dysplasia and Gastric Cancer</atitle><jtitle>Digestive diseases and sciences</jtitle><stitle>Dig Dis Sci</stitle><addtitle>Dig Dis Sci</addtitle><date>2022-08-01</date><risdate>2022</risdate><volume>67</volume><issue>8</issue><spage>3693</spage><epage>3701</epage><pages>3693-3701</pages><issn>0163-2116</issn><eissn>1573-2568</eissn><abstract>Background and Aims
Guidelines cite extensive gastric intestinal metaplasia (GIM) as a bigger risk factor for gastric cancer (GC) than limited GIM and an indication for endoscopic surveillance. Data on progression of extensive GIM to GC in the USA are limited. This study aimed to estimate the prevalence and progression rates of extensive GIM in a US cohort.
Methods
This retrospective study assessed the prevalence of extensive GIM between 1/1/1990 and 8/1/2019 at a large academic medical center. Multivariable regression was used to identify predictors of extensive GIM. Incidence of GC on follow-up was calculated as number of new diagnoses divided by person-years of follow-up. Presence of GIM on subsequent follow-up endoscopy was assessed.
Results
Of 1256 individuals with GIM, 352 (28%) had extensive GIM and 904 (72%) had limited GIM. On multivariable analysis, older age (OR 1.01, 95% CI 1.00–1.02) and Hispanic ethnicity (OR 1.55, 95% CI 1.11–2.16) were predictive of extensive GIM. The annual incidence of GC for GIM overall was 0.09%. There was no difference in progression to GC between extensive or limited GIM (IRR 0, 95% CI 0–2.6), or to advanced lesions overall (IRR 0.37, 95% CI 0.04–1.62). 70% of individuals had persistent GIM on follow-up biopsy, and 22% with limited GIM had extensive GIM on follow-up biopsy.
Conclusions
28% of individuals with GIM have the extensive subtype, and are more likely to be older and of Hispanic ethnicity. There was no difference in progression to GC between extensive and limited GIM. Further research is needed to better assess risk of GIM in the US context.</abstract><cop>New York</cop><pub>Springer US</pub><pmid>34657192</pmid><doi>10.1007/s10620-021-07276-9</doi><tpages>9</tpages><orcidid>https://orcid.org/0000-0001-6816-3293</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Analysis Biochemistry Biopsy Cancer Development and progression Dysplasia Endoscopy Endoscopy, Gastrointestinal Ethnicity Gastric cancer Gastroenterology Health aspects Hepatology Humans Hyperplasia Medical centers Medical colleges Medicine Medicine & Public Health Metaplasia - epidemiology Oncology Original Article Precancerous Conditions - pathology Prevalence Retrospective Studies Stomach cancer Stomach Neoplasms - pathology Transplant Surgery |
title | Prevalence of Extensive and Limited Gastric Intestinal Metaplasia and Progression to Dysplasia and Gastric Cancer |
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