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
Hauptverfasser: Johnston, Simon D, Peter Watson, R G, McMillan, Stanley A, Evans, Alun E, Love, Andrew H.G
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container_issue 3
container_start_page 259
container_title European journal of gastroenterology & hepatology
container_volume 10
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.
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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><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. 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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. 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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 &amp; 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 &amp; 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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