Serological markers for coeliac disease: changes with time and relationship to enteropathy
Antigliadin antibodies (AGA) may be present in healthy adults. One previous study has reported that IgA-AGA detected by population screening may become negative after a 6-year follow-up period. OBJECTIVESTo determine the variability of coeliac disease-associated antibodies with time and to ascertain...
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Veröffentlicht in: | European journal of gastroenterology & hepatology 1998-03, Vol.10 (3), p.259-264 |
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creator | Johnston, Simon D Peter Watson, R G McMillan, Stanley A Evans, Alun E Love, Andrew H.G |
description | Antigliadin antibodies (AGA) may be present in healthy adults. One previous study has reported that IgA-AGA detected by population screening may become negative after a 6-year follow-up period.
OBJECTIVESTo determine the variability of coeliac disease-associated antibodies with time and to ascertain which antibodies are predictive of the presence of enteropathy.
DESIGNA clinical follow-up study of subjects with positive serological markers detected by screening at the time of the Belfast MONICA Project.
METHODSJejunal biopsies were carried out endoscopically by means of a Crosby capsule. IgA-antigliadin was detected by a commercial ELISA; IgA-antiendomysial and antireticulin antibodies were determined by indirect immunofluorescence.
RESULTSOf 48 subjects followed up after 4 years, 28 (58%) had developed negative serology and 20 (42%) had persistently positive serology. Thirteen of 20 subjects with persistent serology had villous atrophy. Of 68 subjects followed up after 13 years, 32 (47%) had developed negative serology and 36 (53%) had persistent serology. Of 10 subjects with persistent serology who were biopsied, four had villous atrophy. None of the subjects who developed negative serology were found to have coeliac disease.
CONCLUSIONSPersistence of serological markers as a follow-up to a population screening programme may predict enteropathy in some subjects, whereas subjects who develop negative serology may be reassured. Subjects with persistent serology and normal histology require follow-up to determine if these markers are indicative of latent coeliac disease. |
doi_str_mv | 10.1097/00042737-199803000-00013 |
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OBJECTIVESTo determine the variability of coeliac disease-associated antibodies with time and to ascertain which antibodies are predictive of the presence of enteropathy.
DESIGNA clinical follow-up study of subjects with positive serological markers detected by screening at the time of the Belfast MONICA Project.
METHODSJejunal biopsies were carried out endoscopically by means of a Crosby capsule. IgA-antigliadin was detected by a commercial ELISA; IgA-antiendomysial and antireticulin antibodies were determined by indirect immunofluorescence.
RESULTSOf 48 subjects followed up after 4 years, 28 (58%) had developed negative serology and 20 (42%) had persistently positive serology. Thirteen of 20 subjects with persistent serology had villous atrophy. Of 68 subjects followed up after 13 years, 32 (47%) had developed negative serology and 36 (53%) had persistent serology. Of 10 subjects with persistent serology who were biopsied, four had villous atrophy. None of the subjects who developed negative serology were found to have coeliac disease.
CONCLUSIONSPersistence of serological markers as a follow-up to a population screening programme may predict enteropathy in some subjects, whereas subjects who develop negative serology may be reassured. Subjects with persistent serology and normal histology require follow-up to determine if these markers are indicative of latent coeliac disease.</description><identifier>ISSN: 0954-691X</identifier><identifier>EISSN: 1473-5687</identifier><identifier>DOI: 10.1097/00042737-199803000-00013</identifier><identifier>PMID: 9585032</identifier><language>eng</language><publisher>Hagerstown, MD: Lippincott-Raven Publishers</publisher><subject>Biological and medical sciences ; Biomarkers - blood ; Biopsy ; Celiac Disease - blood ; Female ; Follow-Up Studies ; Gastroenterology. Liver. Pancreas. Abdomen ; Gliadin - immunology ; Humans ; Immunoglobulin A - blood ; Jejunum - pathology ; Male ; Medical sciences ; Middle Aged ; Muscles - immunology ; Other diseases. Semiology ; Predictive Value of Tests ; Reticulin - immunology ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Time Factors</subject><ispartof>European journal of gastroenterology & hepatology, 1998-03, Vol.10 (3), p.259-264</ispartof><rights>Lippincott-Raven Publishers.</rights><rights>1998 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>314,780,784,27924,27925</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=2208200$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/9585032$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Johnston, Simon D</creatorcontrib><creatorcontrib>Peter Watson, R G</creatorcontrib><creatorcontrib>McMillan, Stanley A</creatorcontrib><creatorcontrib>Evans, Alun E</creatorcontrib><creatorcontrib>Love, Andrew H.G</creatorcontrib><title>Serological markers for coeliac disease: changes with time and relationship to enteropathy</title><title>European journal of gastroenterology & hepatology</title><addtitle>Eur J Gastroenterol Hepatol</addtitle><description>Antigliadin antibodies (AGA) may be present in healthy adults. One previous study has reported that IgA-AGA detected by population screening may become negative after a 6-year follow-up period.
OBJECTIVESTo determine the variability of coeliac disease-associated antibodies with time and to ascertain which antibodies are predictive of the presence of enteropathy.
DESIGNA clinical follow-up study of subjects with positive serological markers detected by screening at the time of the Belfast MONICA Project.
METHODSJejunal biopsies were carried out endoscopically by means of a Crosby capsule. IgA-antigliadin was detected by a commercial ELISA; IgA-antiendomysial and antireticulin antibodies were determined by indirect immunofluorescence.
RESULTSOf 48 subjects followed up after 4 years, 28 (58%) had developed negative serology and 20 (42%) had persistently positive serology. Thirteen of 20 subjects with persistent serology had villous atrophy. Of 68 subjects followed up after 13 years, 32 (47%) had developed negative serology and 36 (53%) had persistent serology. Of 10 subjects with persistent serology who were biopsied, four had villous atrophy. None of the subjects who developed negative serology were found to have coeliac disease.
CONCLUSIONSPersistence of serological markers as a follow-up to a population screening programme may predict enteropathy in some subjects, whereas subjects who develop negative serology may be reassured. Subjects with persistent serology and normal histology require follow-up to determine if these markers are indicative of latent coeliac disease.</description><subject>Biological and medical sciences</subject><subject>Biomarkers - blood</subject><subject>Biopsy</subject><subject>Celiac Disease - blood</subject><subject>Female</subject><subject>Follow-Up Studies</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Gliadin - immunology</subject><subject>Humans</subject><subject>Immunoglobulin A - blood</subject><subject>Jejunum - pathology</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Muscles - immunology</subject><subject>Other diseases. Semiology</subject><subject>Predictive Value of Tests</subject><subject>Reticulin - immunology</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Time Factors</subject><issn>0954-691X</issn><issn>1473-5687</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>1998</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp1kU1vEzEQhi0EKmnLT0DyAXFb8MdubHNDFR-VKvXQHlAv1tg77po662BvFPXfY0jIjYNlWe8zM5rHhFDOPnBm1EfGWC-UVB03RjPZnl07XL4gK94r2Q1rrV6SFTND360N__GanNf6sxFKcnVGzsygBybFijzcYckpP0YPiW6gPGGpNORCfcYUwdMxVoSKn6ifYH7ESvdxmegSN0hhHmnBBEvMc53ili6Z4ry0hltYpudL8ipAqvjmeF-Q-69f7q--dze3366vPt90XgojO_AY9AgwaMcdOtE7DMozIQMYPoY1G5QbXS_Qe-VAsyBHL4fROWdgMEFekPeHttuSf-2wLnYTq8eUYMa8q1YZvVa9lg3UB9CXXGvBYLcltpWfLWf2j1X7z6o9WbV_rbbSt8cZO7fB8VR41Njyd8ccahMZCsw-1hMmBNOCsYb1B2yfU9NUn9Juj8VOCGmZ7P_-VP4G6eaRvw</recordid><startdate>199803</startdate><enddate>199803</enddate><creator>Johnston, Simon D</creator><creator>Peter Watson, R G</creator><creator>McMillan, Stanley A</creator><creator>Evans, Alun E</creator><creator>Love, Andrew H.G</creator><general>Lippincott-Raven Publishers</general><general>Lippincott Williams & Wilkins</general><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>199803</creationdate><title>Serological markers for coeliac disease: changes with time and relationship to enteropathy</title><author>Johnston, Simon D ; Peter Watson, R G ; McMillan, Stanley A ; Evans, Alun E ; Love, Andrew H.G</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c3293-acef8daa58b1beb24bef7c023fa91df6057bdb42ecc7ba80f3dc35dbbb9a59f3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>1998</creationdate><topic>Biological and medical sciences</topic><topic>Biomarkers - blood</topic><topic>Biopsy</topic><topic>Celiac Disease - blood</topic><topic>Female</topic><topic>Follow-Up Studies</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Gliadin - immunology</topic><topic>Humans</topic><topic>Immunoglobulin A - blood</topic><topic>Jejunum - pathology</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Muscles - immunology</topic><topic>Other diseases. Semiology</topic><topic>Predictive Value of Tests</topic><topic>Reticulin - immunology</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Time Factors</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Johnston, Simon D</creatorcontrib><creatorcontrib>Peter Watson, R G</creatorcontrib><creatorcontrib>McMillan, Stanley A</creatorcontrib><creatorcontrib>Evans, Alun E</creatorcontrib><creatorcontrib>Love, Andrew H.G</creatorcontrib><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>European journal of gastroenterology & hepatology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Johnston, Simon D</au><au>Peter Watson, R G</au><au>McMillan, Stanley A</au><au>Evans, Alun E</au><au>Love, Andrew H.G</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serological markers for coeliac disease: changes with time and relationship to enteropathy</atitle><jtitle>European journal of gastroenterology & hepatology</jtitle><addtitle>Eur J Gastroenterol Hepatol</addtitle><date>1998-03</date><risdate>1998</risdate><volume>10</volume><issue>3</issue><spage>259</spage><epage>264</epage><pages>259-264</pages><issn>0954-691X</issn><eissn>1473-5687</eissn><abstract>Antigliadin antibodies (AGA) may be present in healthy adults. One previous study has reported that IgA-AGA detected by population screening may become negative after a 6-year follow-up period.
OBJECTIVESTo determine the variability of coeliac disease-associated antibodies with time and to ascertain which antibodies are predictive of the presence of enteropathy.
DESIGNA clinical follow-up study of subjects with positive serological markers detected by screening at the time of the Belfast MONICA Project.
METHODSJejunal biopsies were carried out endoscopically by means of a Crosby capsule. IgA-antigliadin was detected by a commercial ELISA; IgA-antiendomysial and antireticulin antibodies were determined by indirect immunofluorescence.
RESULTSOf 48 subjects followed up after 4 years, 28 (58%) had developed negative serology and 20 (42%) had persistently positive serology. Thirteen of 20 subjects with persistent serology had villous atrophy. Of 68 subjects followed up after 13 years, 32 (47%) had developed negative serology and 36 (53%) had persistent serology. Of 10 subjects with persistent serology who were biopsied, four had villous atrophy. None of the subjects who developed negative serology were found to have coeliac disease.
CONCLUSIONSPersistence of serological markers as a follow-up to a population screening programme may predict enteropathy in some subjects, whereas subjects who develop negative serology may be reassured. Subjects with persistent serology and normal histology require follow-up to determine if these markers are indicative of latent coeliac disease.</abstract><cop>Hagerstown, MD</cop><pub>Lippincott-Raven Publishers</pub><pmid>9585032</pmid><doi>10.1097/00042737-199803000-00013</doi><tpages>6</tpages></addata></record> |
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subjects | Biological and medical sciences Biomarkers - blood Biopsy Celiac Disease - blood Female Follow-Up Studies Gastroenterology. Liver. Pancreas. Abdomen Gliadin - immunology Humans Immunoglobulin A - blood Jejunum - pathology Male Medical sciences Middle Aged Muscles - immunology Other diseases. Semiology Predictive Value of Tests Reticulin - immunology Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Time Factors |
title | Serological markers for coeliac disease: changes with time and relationship to enteropathy |
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