Association between serrated epithelial changes and colorectal dysplasia in inflammatory bowel disease
Background and Aims Serrated epithelial change (SEC) is a histologic finding in longstanding colitis that may be associated with dysplasia. Our primary aim was to determine the incidence of dysplasia and colorectal cancer (CRC) in inflammatory bowel disease (IBD) patients with SEC. Secondary aims we...
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creator | Parian, Alyssa, MD Koh, Joyce, MD Limketkai, Berkeley N., MD Eluri, Swathi, MD Rubin, David T., MD Brant, Steven R., MD Ha, Christina Y., MD Bayless, Theodore M., MD Giardiello, Francis, MD Hart, John, MD Montgomery, Elizabeth, MD Lazarev, Mark G., MD |
description | Background and Aims Serrated epithelial change (SEC) is a histologic finding in longstanding colitis that may be associated with dysplasia. Our primary aim was to determine the incidence of dysplasia and colorectal cancer (CRC) in inflammatory bowel disease (IBD) patients with SEC. Secondary aims were to determine the rate of location concordance between SEC and dysplasia/CRC and to identify other risk factors associated with dysplasia in IBD patients with SEC. Methods A retrospective, descriptive, observational study was performed by searching the Pathology Data System at a single tertiary referral center for a histologic finding of “serrated epithelial change.” The patient’s first pathology specimen with SEC was designated the index SEC. All subsequent pathology reports were evaluated for the occurrence and location of dysplasia or CRC. Univariable and multivariable logistic regression were performed to identify predictors of dysplasia. Results There were 187 patients with confirmed IBD and 1 or more histologic findings of SEC without prior dysplasia. Mean IBD duration was 16 years, and median follow-up time was 28 months. The rate of high-grade dysplasia or CRC was 17 per 1000 patient-years. Thirty-nine of 187 patients (21%) had synchronous or metachronous dysplasia or CRC. Location concordance was 68%. Multivariable analysis found SEC on follow-up examinations, older age at IBD diagnosis, male gender, and a first-degree relative with CRC were associated with dysplasia in IBD patients with SEC. Conclusions This uncontrolled study describes a high frequency of dysplasia in patients with a histologic finding of SEC. SEC seen on successive endoscopic examinations further increased the risk of dysplasia. Further controlled studies are needed to determine if SEC is a precancerous lesion in IBD patients and if SEC can be endoscopically identified. |
doi_str_mv | 10.1016/j.gie.2015.12.010 |
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fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmedcentral_primary_oai_pubmedcentral_nih_gov_5555397</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><els_id>S0016510715032046</els_id><sourcerecordid>1797869925</sourcerecordid><originalsourceid>FETCH-LOGICAL-c506t-30969c4c23e34784d121d05fa67ebb7468d8c286fcad11c7b8bd2e94cca04c03</originalsourceid><addsrcrecordid>eNp9UtFqFDEUDaLYtfoBvsg8-jJjbmYmmSAUSlFbKPhg30MmubObNZusyWzL_n0zbC3qg-FCIPeck8s5l5D3QBugwD9tm7XDhlHoG2ANBfqCrIBKUXMh5EuyogVU90DFGXmT85ZSOrAWXpMzxgWVAGxFpsuco3F6djFUI84PiKHKmJKe0Va4d_MGvdO-Mhsd1pgrHWxloo8JzVye7THvvc5OVy6Umrze7fQc07Ea4wOWvsuoM74lrybtM757us_J3dcvd1fX9e33bzdXl7e16Smf65ZKLk1nWIttJ4bOAgNL-0lzgeMoOj7YwbCBT0ZbACPGYbQMZWeMpp2h7Tm5OMnuD-MOrcEwJ-3VPrmdTkcVtVN_d4LbqHW8V305rRRF4OOTQIq_DphntXPZoPc6YDxkBUKKgUvJ-gKFE9SkmHPC6fkboGqJR21ViUct8ShgqsRTOB_-nO-Z8TuPAvh8AmAx6d5hUtk4DAatWwxXNrr_yl_8wzbeBWe0_4lHzNt4SKG4r0DlQlA_lv1Y1gN62jLa8fYRdnq4Yg</addsrcrecordid><sourcetype>Open Access Repository</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>1797869925</pqid></control><display><type>article</type><title>Association between serrated epithelial changes and colorectal dysplasia in inflammatory bowel disease</title><source>MEDLINE</source><source>Elsevier ScienceDirect Journals</source><creator>Parian, Alyssa, MD ; Koh, Joyce, MD ; Limketkai, Berkeley N., MD ; Eluri, Swathi, MD ; Rubin, David T., MD ; Brant, Steven R., MD ; Ha, Christina Y., MD ; Bayless, Theodore M., MD ; Giardiello, Francis, MD ; Hart, John, MD ; Montgomery, Elizabeth, MD ; Lazarev, Mark G., MD</creator><creatorcontrib>Parian, Alyssa, MD ; Koh, Joyce, MD ; Limketkai, Berkeley N., MD ; Eluri, Swathi, MD ; Rubin, David T., MD ; Brant, Steven R., MD ; Ha, Christina Y., MD ; Bayless, Theodore M., MD ; Giardiello, Francis, MD ; Hart, John, MD ; Montgomery, Elizabeth, MD ; Lazarev, Mark G., MD</creatorcontrib><description>Background and Aims Serrated epithelial change (SEC) is a histologic finding in longstanding colitis that may be associated with dysplasia. Our primary aim was to determine the incidence of dysplasia and colorectal cancer (CRC) in inflammatory bowel disease (IBD) patients with SEC. Secondary aims were to determine the rate of location concordance between SEC and dysplasia/CRC and to identify other risk factors associated with dysplasia in IBD patients with SEC. Methods A retrospective, descriptive, observational study was performed by searching the Pathology Data System at a single tertiary referral center for a histologic finding of “serrated epithelial change.” The patient’s first pathology specimen with SEC was designated the index SEC. All subsequent pathology reports were evaluated for the occurrence and location of dysplasia or CRC. Univariable and multivariable logistic regression were performed to identify predictors of dysplasia. Results There were 187 patients with confirmed IBD and 1 or more histologic findings of SEC without prior dysplasia. Mean IBD duration was 16 years, and median follow-up time was 28 months. The rate of high-grade dysplasia or CRC was 17 per 1000 patient-years. Thirty-nine of 187 patients (21%) had synchronous or metachronous dysplasia or CRC. Location concordance was 68%. Multivariable analysis found SEC on follow-up examinations, older age at IBD diagnosis, male gender, and a first-degree relative with CRC were associated with dysplasia in IBD patients with SEC. Conclusions This uncontrolled study describes a high frequency of dysplasia in patients with a histologic finding of SEC. SEC seen on successive endoscopic examinations further increased the risk of dysplasia. Further controlled studies are needed to determine if SEC is a precancerous lesion in IBD patients and if SEC can be endoscopically identified.</description><identifier>ISSN: 0016-5107</identifier><identifier>EISSN: 1097-6779</identifier><identifier>DOI: 10.1016/j.gie.2015.12.010</identifier><identifier>PMID: 26709112</identifier><language>eng</language><publisher>United States: Elsevier Inc</publisher><subject>Adenocarcinoma - epidemiology ; Adenocarcinoma - pathology ; Adenoma - epidemiology ; Adenoma - pathology ; Adult ; Aged ; Colon - pathology ; Colorectal Neoplasms - epidemiology ; Colorectal Neoplasms - pathology ; Female ; Gastroenterology and Hepatology ; Humans ; Incidence ; Inflammatory Bowel Diseases - epidemiology ; Logistic Models ; Male ; Middle Aged ; Multivariate Analysis ; Neoplasm Grading ; Odds Ratio ; Precancerous Conditions - epidemiology ; Precancerous Conditions - pathology ; Retrospective Studies ; Risk Factors ; Sex Factors ; United States</subject><ispartof>Gastrointestinal endoscopy, 2016-07, Vol.84 (1), p.87-95.e1</ispartof><rights>American Society for Gastrointestinal Endoscopy</rights><rights>2016 American Society for Gastrointestinal Endoscopy</rights><rights>Copyright © 2016 American Society for Gastrointestinal Endoscopy. Published by Elsevier Inc. All rights reserved.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c506t-30969c4c23e34784d121d05fa67ebb7468d8c286fcad11c7b8bd2e94cca04c03</citedby><cites>FETCH-LOGICAL-c506t-30969c4c23e34784d121d05fa67ebb7468d8c286fcad11c7b8bd2e94cca04c03</cites><orcidid>0000-0001-9995-7942</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktohtml>$$Uhttps://www.sciencedirect.com/science/article/pii/S0016510715032046$$EHTML$$P50$$Gelsevier$$H</linktohtml><link.rule.ids>230,314,776,780,881,3537,27901,27902,65306</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/26709112$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Parian, Alyssa, MD</creatorcontrib><creatorcontrib>Koh, Joyce, MD</creatorcontrib><creatorcontrib>Limketkai, Berkeley N., MD</creatorcontrib><creatorcontrib>Eluri, Swathi, MD</creatorcontrib><creatorcontrib>Rubin, David T., MD</creatorcontrib><creatorcontrib>Brant, Steven R., MD</creatorcontrib><creatorcontrib>Ha, Christina Y., MD</creatorcontrib><creatorcontrib>Bayless, Theodore M., MD</creatorcontrib><creatorcontrib>Giardiello, Francis, MD</creatorcontrib><creatorcontrib>Hart, John, MD</creatorcontrib><creatorcontrib>Montgomery, Elizabeth, MD</creatorcontrib><creatorcontrib>Lazarev, Mark G., MD</creatorcontrib><title>Association between serrated epithelial changes and colorectal dysplasia in inflammatory bowel disease</title><title>Gastrointestinal endoscopy</title><addtitle>Gastrointest Endosc</addtitle><description>Background and Aims Serrated epithelial change (SEC) is a histologic finding in longstanding colitis that may be associated with dysplasia. Our primary aim was to determine the incidence of dysplasia and colorectal cancer (CRC) in inflammatory bowel disease (IBD) patients with SEC. Secondary aims were to determine the rate of location concordance between SEC and dysplasia/CRC and to identify other risk factors associated with dysplasia in IBD patients with SEC. Methods A retrospective, descriptive, observational study was performed by searching the Pathology Data System at a single tertiary referral center for a histologic finding of “serrated epithelial change.” The patient’s first pathology specimen with SEC was designated the index SEC. All subsequent pathology reports were evaluated for the occurrence and location of dysplasia or CRC. Univariable and multivariable logistic regression were performed to identify predictors of dysplasia. Results There were 187 patients with confirmed IBD and 1 or more histologic findings of SEC without prior dysplasia. Mean IBD duration was 16 years, and median follow-up time was 28 months. The rate of high-grade dysplasia or CRC was 17 per 1000 patient-years. Thirty-nine of 187 patients (21%) had synchronous or metachronous dysplasia or CRC. Location concordance was 68%. Multivariable analysis found SEC on follow-up examinations, older age at IBD diagnosis, male gender, and a first-degree relative with CRC were associated with dysplasia in IBD patients with SEC. Conclusions This uncontrolled study describes a high frequency of dysplasia in patients with a histologic finding of SEC. SEC seen on successive endoscopic examinations further increased the risk of dysplasia. Further controlled studies are needed to determine if SEC is a precancerous lesion in IBD patients and if SEC can be endoscopically identified.</description><subject>Adenocarcinoma - epidemiology</subject><subject>Adenocarcinoma - pathology</subject><subject>Adenoma - epidemiology</subject><subject>Adenoma - pathology</subject><subject>Adult</subject><subject>Aged</subject><subject>Colon - pathology</subject><subject>Colorectal Neoplasms - epidemiology</subject><subject>Colorectal Neoplasms - pathology</subject><subject>Female</subject><subject>Gastroenterology and Hepatology</subject><subject>Humans</subject><subject>Incidence</subject><subject>Inflammatory Bowel Diseases - epidemiology</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Middle Aged</subject><subject>Multivariate Analysis</subject><subject>Neoplasm Grading</subject><subject>Odds Ratio</subject><subject>Precancerous Conditions - epidemiology</subject><subject>Precancerous Conditions - pathology</subject><subject>Retrospective Studies</subject><subject>Risk Factors</subject><subject>Sex Factors</subject><subject>United States</subject><issn>0016-5107</issn><issn>1097-6779</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2016</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9UtFqFDEUDaLYtfoBvsg8-jJjbmYmmSAUSlFbKPhg30MmubObNZusyWzL_n0zbC3qg-FCIPeck8s5l5D3QBugwD9tm7XDhlHoG2ANBfqCrIBKUXMh5EuyogVU90DFGXmT85ZSOrAWXpMzxgWVAGxFpsuco3F6djFUI84PiKHKmJKe0Va4d_MGvdO-Mhsd1pgrHWxloo8JzVye7THvvc5OVy6Umrze7fQc07Ea4wOWvsuoM74lrybtM757us_J3dcvd1fX9e33bzdXl7e16Smf65ZKLk1nWIttJ4bOAgNL-0lzgeMoOj7YwbCBT0ZbACPGYbQMZWeMpp2h7Tm5OMnuD-MOrcEwJ-3VPrmdTkcVtVN_d4LbqHW8V305rRRF4OOTQIq_DphntXPZoPc6YDxkBUKKgUvJ-gKFE9SkmHPC6fkboGqJR21ViUct8ShgqsRTOB_-nO-Z8TuPAvh8AmAx6d5hUtk4DAatWwxXNrr_yl_8wzbeBWe0_4lHzNt4SKG4r0DlQlA_lv1Y1gN62jLa8fYRdnq4Yg</recordid><startdate>20160701</startdate><enddate>20160701</enddate><creator>Parian, Alyssa, MD</creator><creator>Koh, Joyce, MD</creator><creator>Limketkai, Berkeley N., MD</creator><creator>Eluri, Swathi, MD</creator><creator>Rubin, David T., MD</creator><creator>Brant, Steven R., MD</creator><creator>Ha, Christina Y., MD</creator><creator>Bayless, Theodore M., MD</creator><creator>Giardiello, Francis, MD</creator><creator>Hart, John, MD</creator><creator>Montgomery, Elizabeth, MD</creator><creator>Lazarev, Mark G., MD</creator><general>Elsevier Inc</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>7X8</scope><scope>5PM</scope><orcidid>https://orcid.org/0000-0001-9995-7942</orcidid></search><sort><creationdate>20160701</creationdate><title>Association between serrated epithelial changes and colorectal dysplasia in inflammatory bowel disease</title><author>Parian, Alyssa, MD ; Koh, Joyce, MD ; Limketkai, Berkeley N., MD ; Eluri, Swathi, MD ; Rubin, David T., MD ; Brant, Steven R., MD ; Ha, Christina Y., MD ; Bayless, Theodore M., MD ; Giardiello, Francis, MD ; Hart, John, MD ; Montgomery, Elizabeth, MD ; Lazarev, Mark G., MD</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c506t-30969c4c23e34784d121d05fa67ebb7468d8c286fcad11c7b8bd2e94cca04c03</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2016</creationdate><topic>Adenocarcinoma - epidemiology</topic><topic>Adenocarcinoma - pathology</topic><topic>Adenoma - epidemiology</topic><topic>Adenoma - pathology</topic><topic>Adult</topic><topic>Aged</topic><topic>Colon - pathology</topic><topic>Colorectal Neoplasms - epidemiology</topic><topic>Colorectal Neoplasms - pathology</topic><topic>Female</topic><topic>Gastroenterology and Hepatology</topic><topic>Humans</topic><topic>Incidence</topic><topic>Inflammatory Bowel Diseases - epidemiology</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Middle Aged</topic><topic>Multivariate Analysis</topic><topic>Neoplasm Grading</topic><topic>Odds Ratio</topic><topic>Precancerous Conditions - epidemiology</topic><topic>Precancerous Conditions - pathology</topic><topic>Retrospective Studies</topic><topic>Risk Factors</topic><topic>Sex Factors</topic><topic>United States</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Parian, Alyssa, MD</creatorcontrib><creatorcontrib>Koh, Joyce, MD</creatorcontrib><creatorcontrib>Limketkai, Berkeley N., MD</creatorcontrib><creatorcontrib>Eluri, Swathi, MD</creatorcontrib><creatorcontrib>Rubin, David T., MD</creatorcontrib><creatorcontrib>Brant, Steven R., MD</creatorcontrib><creatorcontrib>Ha, Christina Y., MD</creatorcontrib><creatorcontrib>Bayless, Theodore M., MD</creatorcontrib><creatorcontrib>Giardiello, Francis, MD</creatorcontrib><creatorcontrib>Hart, John, MD</creatorcontrib><creatorcontrib>Montgomery, Elizabeth, MD</creatorcontrib><creatorcontrib>Lazarev, Mark G., MD</creatorcontrib><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>Gastrointestinal endoscopy</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Parian, Alyssa, MD</au><au>Koh, Joyce, MD</au><au>Limketkai, Berkeley N., MD</au><au>Eluri, Swathi, MD</au><au>Rubin, David T., MD</au><au>Brant, Steven R., MD</au><au>Ha, Christina Y., MD</au><au>Bayless, Theodore M., MD</au><au>Giardiello, Francis, MD</au><au>Hart, John, MD</au><au>Montgomery, Elizabeth, MD</au><au>Lazarev, Mark G., MD</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Association between serrated epithelial changes and colorectal dysplasia in inflammatory bowel disease</atitle><jtitle>Gastrointestinal endoscopy</jtitle><addtitle>Gastrointest Endosc</addtitle><date>2016-07-01</date><risdate>2016</risdate><volume>84</volume><issue>1</issue><spage>87</spage><epage>95.e1</epage><pages>87-95.e1</pages><issn>0016-5107</issn><eissn>1097-6779</eissn><abstract>Background and Aims Serrated epithelial change (SEC) is a histologic finding in longstanding colitis that may be associated with dysplasia. Our primary aim was to determine the incidence of dysplasia and colorectal cancer (CRC) in inflammatory bowel disease (IBD) patients with SEC. Secondary aims were to determine the rate of location concordance between SEC and dysplasia/CRC and to identify other risk factors associated with dysplasia in IBD patients with SEC. Methods A retrospective, descriptive, observational study was performed by searching the Pathology Data System at a single tertiary referral center for a histologic finding of “serrated epithelial change.” The patient’s first pathology specimen with SEC was designated the index SEC. All subsequent pathology reports were evaluated for the occurrence and location of dysplasia or CRC. Univariable and multivariable logistic regression were performed to identify predictors of dysplasia. Results There were 187 patients with confirmed IBD and 1 or more histologic findings of SEC without prior dysplasia. Mean IBD duration was 16 years, and median follow-up time was 28 months. The rate of high-grade dysplasia or CRC was 17 per 1000 patient-years. Thirty-nine of 187 patients (21%) had synchronous or metachronous dysplasia or CRC. Location concordance was 68%. Multivariable analysis found SEC on follow-up examinations, older age at IBD diagnosis, male gender, and a first-degree relative with CRC were associated with dysplasia in IBD patients with SEC. Conclusions This uncontrolled study describes a high frequency of dysplasia in patients with a histologic finding of SEC. SEC seen on successive endoscopic examinations further increased the risk of dysplasia. Further controlled studies are needed to determine if SEC is a precancerous lesion in IBD patients and if SEC can be endoscopically identified.</abstract><cop>United States</cop><pub>Elsevier Inc</pub><pmid>26709112</pmid><doi>10.1016/j.gie.2015.12.010</doi><orcidid>https://orcid.org/0000-0001-9995-7942</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Adenocarcinoma - epidemiology Adenocarcinoma - pathology Adenoma - epidemiology Adenoma - pathology Adult Aged Colon - pathology Colorectal Neoplasms - epidemiology Colorectal Neoplasms - pathology Female Gastroenterology and Hepatology Humans Incidence Inflammatory Bowel Diseases - epidemiology Logistic Models Male Middle Aged Multivariate Analysis Neoplasm Grading Odds Ratio Precancerous Conditions - epidemiology Precancerous Conditions - pathology Retrospective Studies Risk Factors Sex Factors United States |
title | Association between serrated epithelial changes and colorectal dysplasia in inflammatory bowel disease |
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