Serum biomarkers provide an accurate method for diagnosis of atrophic gastritis in a general population: The Kalixanda study
Objective. Serological biomarkers can be used for non-invasive diagnosis of gastritis and atrophic gastritis. The aim of this study was to compare the validity of serum levels of pepsinogen I (PGI) and II (PGII), gastrin-17 (G-17) and Helicobacter pylori antibodies (Hpab) with that of the gold stand...
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Veröffentlicht in: | Scandinavian journal of gastroenterology 2008, Vol.43 (12), p.1448-1455 |
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container_title | Scandinavian journal of gastroenterology |
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creator | Storskrubb, Tom Aro, Pertti Ronkainen, Jukka Sipponen, Pentti Nyhlin, Henry Talley, Nicholas J Engstrand, Lars Stolte, Manfred Vieth, Michael Walker, Marjorie Agréus, Lars |
description | Objective. Serological biomarkers can be used for non-invasive diagnosis of gastritis and atrophic gastritis. The aim of this study was to compare the validity of serum levels of pepsinogen I (PGI) and II (PGII), gastrin-17 (G-17) and Helicobacter pylori antibodies (Hpab) with that of the gold standard histology for diagnosis of atrophic gastritis in a population sample from Northern Sweden. Material and methods. In all, 1000 subjects underwent endoscopies with biopsies. Serum biomarkers were available in 976 subjects for independent diagnosis of gastric mucosal status using a predetermined diagnostic algorithm. Results. Overall agreement between histology and serological biomarkers in diagnosing corpus atrophy was 96% (CI 95%: 95-97%). Sensitivity and specificity of markers for atrophic gastritis were 71% (CI 68-74%) and 98% (CI 97-99%) respectively, corresponding to 69% (CI 95%: 66-72%) and 98% (95% CI 97-99%) positive and negative predictive values. The positive likelihood ratio was 35.5 (95% CI: 35.0-36.0%). In subgroups with normal stomachs, H. pylori non-atrophic gastritis and H. pylori-negative gastritis by histology, the prevalence of corpus atrophy diagnosed with the biomarkers was 0.8% and 4.9%, respectively. In total, 6.6% of subjects in the study population had corpus atrophy according to the serological biomarkers. Conclusions. Serological biomarkers show a high degree of accuracy as a non-invasive method to diagnose corpus atrophy, which is common in the general population. |
doi_str_mv | 10.1080/00365520802273025 |
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Serological biomarkers can be used for non-invasive diagnosis of gastritis and atrophic gastritis. The aim of this study was to compare the validity of serum levels of pepsinogen I (PGI) and II (PGII), gastrin-17 (G-17) and Helicobacter pylori antibodies (Hpab) with that of the gold standard histology for diagnosis of atrophic gastritis in a population sample from Northern Sweden. Material and methods. In all, 1000 subjects underwent endoscopies with biopsies. Serum biomarkers were available in 976 subjects for independent diagnosis of gastric mucosal status using a predetermined diagnostic algorithm. Results. Overall agreement between histology and serological biomarkers in diagnosing corpus atrophy was 96% (CI 95%: 95-97%). Sensitivity and specificity of markers for atrophic gastritis were 71% (CI 68-74%) and 98% (CI 97-99%) respectively, corresponding to 69% (CI 95%: 66-72%) and 98% (95% CI 97-99%) positive and negative predictive values. The positive likelihood ratio was 35.5 (95% CI: 35.0-36.0%). In subgroups with normal stomachs, H. pylori non-atrophic gastritis and H. pylori-negative gastritis by histology, the prevalence of corpus atrophy diagnosed with the biomarkers was 0.8% and 4.9%, respectively. In total, 6.6% of subjects in the study population had corpus atrophy according to the serological biomarkers. Conclusions. Serological biomarkers show a high degree of accuracy as a non-invasive method to diagnose corpus atrophy, which is common in the general population.</description><identifier>ISSN: 0036-5521</identifier><identifier>EISSN: 1502-7708</identifier><identifier>DOI: 10.1080/00365520802273025</identifier><identifier>PMID: 18663663</identifier><identifier>CODEN: SJGRA4</identifier><language>eng</language><publisher>Colchester: Informa UK Ltd</publisher><subject>Antibodies, Bacterial - blood ; Atrophic gastritis ; Bacterial diseases ; Bacterial diseases of the digestive system and abdomen ; Biological and medical sciences ; biological markers ; Biomarkers - blood ; Female ; Gastrins - blood ; gastritis ; Gastritis, Atrophic - blood ; Gastritis, Atrophic - diagnosis ; Gastritis, Atrophic - pathology ; Gastroenterology. Liver. Pancreas. Abdomen ; Helicobacter pylori ; Helicobacter pylori - immunology ; Human bacterial diseases ; Humans ; Infectious diseases ; Male ; Medical sciences ; Middle Aged ; Other diseases. Semiology ; Pepsinogen A - blood ; Pepsinogen C - blood ; Reproducibility of Results ; Sensitivity and Specificity ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><ispartof>Scandinavian journal of gastroenterology, 2008, Vol.43 (12), p.1448-1455</ispartof><rights>2008 Informa UK Ltd All rights reserved: reproduction in whole or part not permitted 2008</rights><rights>2009 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c538t-44a778b409c211a442b86697d6e1a11e2de51c681c628f7a8e4586808e180fda3</citedby><cites>FETCH-LOGICAL-c538t-44a778b409c211a442b86697d6e1a11e2de51c681c628f7a8e4586808e180fda3</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.tandfonline.com/doi/pdf/10.1080/00365520802273025$$EPDF$$P50$$Ginformaworld$$H</linktopdf><linktohtml>$$Uhttps://www.tandfonline.com/doi/full/10.1080/00365520802273025$$EHTML$$P50$$Ginformaworld$$H</linktohtml><link.rule.ids>230,314,780,784,885,4022,27922,27923,27924,59646,59752,60435,60541,61220,61255,61401,61436</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&idt=20938892$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/18663663$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink><backlink>$$Uhttp://kipublications.ki.se/Default.aspx?queryparsed=id:117921623$$DView record from Swedish Publication Index$$Hfree_for_read</backlink></links><search><creatorcontrib>Storskrubb, Tom</creatorcontrib><creatorcontrib>Aro, Pertti</creatorcontrib><creatorcontrib>Ronkainen, Jukka</creatorcontrib><creatorcontrib>Sipponen, Pentti</creatorcontrib><creatorcontrib>Nyhlin, Henry</creatorcontrib><creatorcontrib>Talley, Nicholas J</creatorcontrib><creatorcontrib>Engstrand, Lars</creatorcontrib><creatorcontrib>Stolte, Manfred</creatorcontrib><creatorcontrib>Vieth, Michael</creatorcontrib><creatorcontrib>Walker, Marjorie</creatorcontrib><creatorcontrib>Agréus, Lars</creatorcontrib><title>Serum biomarkers provide an accurate method for diagnosis of atrophic gastritis in a general population: The Kalixanda study</title><title>Scandinavian journal of gastroenterology</title><addtitle>Scand J Gastroenterol</addtitle><description>Objective. Serological biomarkers can be used for non-invasive diagnosis of gastritis and atrophic gastritis. The aim of this study was to compare the validity of serum levels of pepsinogen I (PGI) and II (PGII), gastrin-17 (G-17) and Helicobacter pylori antibodies (Hpab) with that of the gold standard histology for diagnosis of atrophic gastritis in a population sample from Northern Sweden. Material and methods. In all, 1000 subjects underwent endoscopies with biopsies. Serum biomarkers were available in 976 subjects for independent diagnosis of gastric mucosal status using a predetermined diagnostic algorithm. Results. Overall agreement between histology and serological biomarkers in diagnosing corpus atrophy was 96% (CI 95%: 95-97%). Sensitivity and specificity of markers for atrophic gastritis were 71% (CI 68-74%) and 98% (CI 97-99%) respectively, corresponding to 69% (CI 95%: 66-72%) and 98% (95% CI 97-99%) positive and negative predictive values. The positive likelihood ratio was 35.5 (95% CI: 35.0-36.0%). In subgroups with normal stomachs, H. pylori non-atrophic gastritis and H. pylori-negative gastritis by histology, the prevalence of corpus atrophy diagnosed with the biomarkers was 0.8% and 4.9%, respectively. In total, 6.6% of subjects in the study population had corpus atrophy according to the serological biomarkers. Conclusions. Serological biomarkers show a high degree of accuracy as a non-invasive method to diagnose corpus atrophy, which is common in the general population.</description><subject>Antibodies, Bacterial - blood</subject><subject>Atrophic gastritis</subject><subject>Bacterial diseases</subject><subject>Bacterial diseases of the digestive system and abdomen</subject><subject>Biological and medical sciences</subject><subject>biological markers</subject><subject>Biomarkers - blood</subject><subject>Female</subject><subject>Gastrins - blood</subject><subject>gastritis</subject><subject>Gastritis, Atrophic - blood</subject><subject>Gastritis, Atrophic - diagnosis</subject><subject>Gastritis, Atrophic - pathology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Helicobacter pylori</subject><subject>Helicobacter pylori - immunology</subject><subject>Human bacterial diseases</subject><subject>Humans</subject><subject>Infectious diseases</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Other diseases. Semiology</subject><subject>Pepsinogen A - blood</subject><subject>Pepsinogen C - blood</subject><subject>Reproducibility of Results</subject><subject>Sensitivity and Specificity</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><issn>0036-5521</issn><issn>1502-7708</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2008</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNp9kV1rFTEQhoMo9rT6A7yR3OjdapL9ympvpNQPLHhhvQ6zyew5abObNclaD_jjTTlrRYRChgyT5x1m8hLyjLNXnEn2mrGyqWuRUyHakon6AdnwmomibZl8SDa370UG-BE5jvGKMVa3VfeYHHHZNGU-G_LrK4ZlpL31I4RrDJHOwf-wBilMFLReAiSkI6adN3TwgRoL28lHG6kfKKTg553VdAsxBZty1WYZ3eKEARyd_bw4SNZPb-jlDulncPYnTAZoTIvZPyGPBnARn673Cfn2_vzy7GNx8eXDp7N3F4WuS5mKqoK2lX3FOi04h6oSfZ6_a02DHDhHYbDmupE5hBxakFjVspFMIpdsMFCekOLQN97gvPRqDjZvu1cerFpL1zlDVTclY03mXx74_BffF4xJjTZqdA4m9EtUTSfLjMkM8gOog48x4HDXmjN1a5H6z6Kseb42X_oRzV_F6kkGXqwARA1uCDBpG-84wbpSyk5k7vTA2SkbM8KND86oBHvnwx9Red8cb_-R7xBc2mkIqK78EqZsyD1b_AaP87-B</recordid><startdate>2008</startdate><enddate>2008</enddate><creator>Storskrubb, Tom</creator><creator>Aro, Pertti</creator><creator>Ronkainen, Jukka</creator><creator>Sipponen, Pentti</creator><creator>Nyhlin, Henry</creator><creator>Talley, Nicholas J</creator><creator>Engstrand, Lars</creator><creator>Stolte, Manfred</creator><creator>Vieth, Michael</creator><creator>Walker, Marjorie</creator><creator>Agréus, Lars</creator><general>Informa UK Ltd</general><general>Taylor & Francis</general><general>Informa</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><scope>ADTPV</scope><scope>AOWAS</scope></search><sort><creationdate>2008</creationdate><title>Serum biomarkers provide an accurate method for diagnosis of atrophic gastritis in a general population: The Kalixanda study</title><author>Storskrubb, Tom ; Aro, Pertti ; Ronkainen, Jukka ; Sipponen, Pentti ; Nyhlin, Henry ; Talley, Nicholas J ; Engstrand, Lars ; Stolte, Manfred ; Vieth, Michael ; Walker, Marjorie ; Agréus, Lars</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c538t-44a778b409c211a442b86697d6e1a11e2de51c681c628f7a8e4586808e180fda3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2008</creationdate><topic>Antibodies, Bacterial - blood</topic><topic>Atrophic gastritis</topic><topic>Bacterial diseases</topic><topic>Bacterial diseases of the digestive system and abdomen</topic><topic>Biological and medical sciences</topic><topic>biological markers</topic><topic>Biomarkers - blood</topic><topic>Female</topic><topic>Gastrins - blood</topic><topic>gastritis</topic><topic>Gastritis, Atrophic - blood</topic><topic>Gastritis, Atrophic - diagnosis</topic><topic>Gastritis, Atrophic - pathology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Helicobacter pylori</topic><topic>Helicobacter pylori - immunology</topic><topic>Human bacterial diseases</topic><topic>Humans</topic><topic>Infectious diseases</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Other diseases. Semiology</topic><topic>Pepsinogen A - blood</topic><topic>Pepsinogen C - blood</topic><topic>Reproducibility of Results</topic><topic>Sensitivity and Specificity</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Storskrubb, Tom</creatorcontrib><creatorcontrib>Aro, Pertti</creatorcontrib><creatorcontrib>Ronkainen, Jukka</creatorcontrib><creatorcontrib>Sipponen, Pentti</creatorcontrib><creatorcontrib>Nyhlin, Henry</creatorcontrib><creatorcontrib>Talley, Nicholas J</creatorcontrib><creatorcontrib>Engstrand, Lars</creatorcontrib><creatorcontrib>Stolte, Manfred</creatorcontrib><creatorcontrib>Vieth, Michael</creatorcontrib><creatorcontrib>Walker, Marjorie</creatorcontrib><creatorcontrib>Agréus, Lars</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><collection>SwePub</collection><collection>SwePub Articles</collection><jtitle>Scandinavian journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Storskrubb, Tom</au><au>Aro, Pertti</au><au>Ronkainen, Jukka</au><au>Sipponen, Pentti</au><au>Nyhlin, Henry</au><au>Talley, Nicholas J</au><au>Engstrand, Lars</au><au>Stolte, Manfred</au><au>Vieth, Michael</au><au>Walker, Marjorie</au><au>Agréus, Lars</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Serum biomarkers provide an accurate method for diagnosis of atrophic gastritis in a general population: The Kalixanda study</atitle><jtitle>Scandinavian journal of gastroenterology</jtitle><addtitle>Scand J Gastroenterol</addtitle><date>2008</date><risdate>2008</risdate><volume>43</volume><issue>12</issue><spage>1448</spage><epage>1455</epage><pages>1448-1455</pages><issn>0036-5521</issn><eissn>1502-7708</eissn><coden>SJGRA4</coden><abstract>Objective. Serological biomarkers can be used for non-invasive diagnosis of gastritis and atrophic gastritis. The aim of this study was to compare the validity of serum levels of pepsinogen I (PGI) and II (PGII), gastrin-17 (G-17) and Helicobacter pylori antibodies (Hpab) with that of the gold standard histology for diagnosis of atrophic gastritis in a population sample from Northern Sweden. Material and methods. In all, 1000 subjects underwent endoscopies with biopsies. Serum biomarkers were available in 976 subjects for independent diagnosis of gastric mucosal status using a predetermined diagnostic algorithm. Results. Overall agreement between histology and serological biomarkers in diagnosing corpus atrophy was 96% (CI 95%: 95-97%). Sensitivity and specificity of markers for atrophic gastritis were 71% (CI 68-74%) and 98% (CI 97-99%) respectively, corresponding to 69% (CI 95%: 66-72%) and 98% (95% CI 97-99%) positive and negative predictive values. The positive likelihood ratio was 35.5 (95% CI: 35.0-36.0%). In subgroups with normal stomachs, H. pylori non-atrophic gastritis and H. pylori-negative gastritis by histology, the prevalence of corpus atrophy diagnosed with the biomarkers was 0.8% and 4.9%, respectively. In total, 6.6% of subjects in the study population had corpus atrophy according to the serological biomarkers. Conclusions. Serological biomarkers show a high degree of accuracy as a non-invasive method to diagnose corpus atrophy, which is common in the general population.</abstract><cop>Colchester</cop><pub>Informa UK Ltd</pub><pmid>18663663</pmid><doi>10.1080/00365520802273025</doi><tpages>8</tpages></addata></record> |
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subjects | Antibodies, Bacterial - blood Atrophic gastritis Bacterial diseases Bacterial diseases of the digestive system and abdomen Biological and medical sciences biological markers Biomarkers - blood Female Gastrins - blood gastritis Gastritis, Atrophic - blood Gastritis, Atrophic - diagnosis Gastritis, Atrophic - pathology Gastroenterology. Liver. Pancreas. Abdomen Helicobacter pylori Helicobacter pylori - immunology Human bacterial diseases Humans Infectious diseases Male Medical sciences Middle Aged Other diseases. Semiology Pepsinogen A - blood Pepsinogen C - blood Reproducibility of Results Sensitivity and Specificity Stomach. Duodenum. Small intestine. Colon. Rectum. Anus |
title | Serum biomarkers provide an accurate method for diagnosis of atrophic gastritis in a general population: The Kalixanda study |
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