Correlation Between IgA Tissue Transglutaminase Antibody Ratio and Histological Finding in Celiac Disease

ABSTRACT Objectives: Positivity of both immumoglobulin A anti‐tissue transglutaminase (TTG) and anti‐endomysium antibodies (EMA) has a positive predictive value of nearly 100% for celiac disease (CD). The objective of the present study was to evaluate whether patients of any age, with high pretest p...

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Veröffentlicht in:Journal of pediatric gastroenterology and nutrition 2012-07, Vol.55 (1), p.44-49
Hauptverfasser: Alessio, Maria G., Tonutti, Elio, Brusca, Ignazio, Radice, Antonella, Licini, Lisa, Sonzogni, Aurelio, Florena, Ada, Schiaffino, Eugenio, Marus, Wally, Sulfaro, Sandro, Villalta, Danilo
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container_end_page 49
container_issue 1
container_start_page 44
container_title Journal of pediatric gastroenterology and nutrition
container_volume 55
creator Alessio, Maria G.
Tonutti, Elio
Brusca, Ignazio
Radice, Antonella
Licini, Lisa
Sonzogni, Aurelio
Florena, Ada
Schiaffino, Eugenio
Marus, Wally
Sulfaro, Sandro
Villalta, Danilo
description ABSTRACT Objectives: Positivity of both immumoglobulin A anti‐tissue transglutaminase (TTG) and anti‐endomysium antibodies (EMA) has a positive predictive value of nearly 100% for celiac disease (CD). The objective of the present study was to evaluate whether patients of any age, with high pretest probability of CD and high titre of anti‐TTG and EMA positivity, have a high probability of intestinal damage and may not require the biopsy for final diagnosis. Methods: A retrospective analysis of 412 consecutively referred patients, age range 10 months to 72 years, who underwent small‐bowel biopsy for suspicion of CD and positivity to both anti‐TTG and EMA, was performed at 4 Italian centers. Biopsies were evaluated independently by 2 pathologists using Marsh modified classification; in cases of dissimilar results, a third pathologist examined the biopsy. The final histological finding diagnosis was expressed as the prevalent or highest score assigned by the pathologist board. Results: Three hundred ninety‐six patients (96.1%) had histological findings consistent with CD (grade 2 and 3a, 3b, or 3c of modified Marsh classification). An anti‐TTG ratio ≥7 was able to identify with the 3 assays used (Celikey, anti‐TTG immumoglobulin A, EuTTG) all of the patients with significant mucosal damage (Marsh ≥2) independent of age and sex; specificity and positive predictive value were 100%. An anti‐TTG ratio >20 was more specific (99.8%) for identification of patients with villous atrophy (Marsh 3 a, b, or c). Conclusions: Patients with positivity of anti‐TTG ≥7‐fold cutoff, confirmed by positivity to EMA, have a high‐degree probability of duodenal damage. In selected conditions, a duodenal biopsy may be avoided and a confirmed greatly positive anti‐TTG result could be the basis to prescribe a gluten‐free diet.
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The objective of the present study was to evaluate whether patients of any age, with high pretest probability of CD and high titre of anti‐TTG and EMA positivity, have a high probability of intestinal damage and may not require the biopsy for final diagnosis. Methods: A retrospective analysis of 412 consecutively referred patients, age range 10 months to 72 years, who underwent small‐bowel biopsy for suspicion of CD and positivity to both anti‐TTG and EMA, was performed at 4 Italian centers. Biopsies were evaluated independently by 2 pathologists using Marsh modified classification; in cases of dissimilar results, a third pathologist examined the biopsy. The final histological finding diagnosis was expressed as the prevalent or highest score assigned by the pathologist board. Results: Three hundred ninety‐six patients (96.1%) had histological findings consistent with CD (grade 2 and 3a, 3b, or 3c of modified Marsh classification). An anti‐TTG ratio ≥7 was able to identify with the 3 assays used (Celikey, anti‐TTG immumoglobulin A, EuTTG) all of the patients with significant mucosal damage (Marsh ≥2) independent of age and sex; specificity and positive predictive value were 100%. An anti‐TTG ratio &gt;20 was more specific (99.8%) for identification of patients with villous atrophy (Marsh 3 a, b, or c). Conclusions: Patients with positivity of anti‐TTG ≥7‐fold cutoff, confirmed by positivity to EMA, have a high‐degree probability of duodenal damage. In selected conditions, a duodenal biopsy may be avoided and a confirmed greatly positive anti‐TTG result could be the basis to prescribe a gluten‐free diet.</description><identifier>ISSN: 0277-2116</identifier><identifier>EISSN: 1536-4801</identifier><identifier>DOI: 10.1097/MPG.0b013e3182470249</identifier><identifier>PMID: 22197946</identifier><identifier>CODEN: JPGND6</identifier><language>eng</language><publisher>Hagerstown, MD: Copyright by ESPGHAN and NASPGHAN</publisher><subject>Adolescent ; Adult ; Aged ; anti‐TTG ratio ; Biological and medical sciences ; Biopsy ; celiac disease ; Celiac Disease - classification ; Celiac Disease - immunology ; Celiac Disease - pathology ; Child ; Child, Preschool ; Duodenum - pathology ; Feeding. Feeding behavior ; Female ; Fundamental and applied biological sciences. Psychology ; Gastroenterology. Liver. Pancreas. Abdomen ; GTP-Binding Proteins - immunology ; Humans ; Immunoglobulin A - blood ; Infant ; Logistic Models ; Male ; Medical sciences ; Middle Aged ; mucosal damage ; Muscles - immunology ; Other diseases. Semiology ; Predictive Value of Tests ; Retrospective Studies ; Severity of Illness Index ; Statistics, Nonparametric ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Transglutaminases - immunology ; Vertebrates: anatomy and physiology, studies on body, several organs or systems ; Young Adult</subject><ispartof>Journal of pediatric gastroenterology and nutrition, 2012-07, Vol.55 (1), p.44-49</ispartof><rights>2012 by European Society for European Society for Pediatric Gastroenterology, Hepatology, and Nutrition and North American Society for Pediatric Gastroenterology, Hepatology, and Nutrition</rights><rights>Copyright 2012 by ESPGHAN and NASPGHAN</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c4869-8ab617821fdd108c33744fc744cd6de08d80fe18444e3d967886a247c55037963</citedby><cites>FETCH-LOGICAL-c4869-8ab617821fdd108c33744fc744cd6de08d80fe18444e3d967886a247c55037963</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://onlinelibrary.wiley.com/doi/pdf/10.1097%2FMPG.0b013e3182470249$$EPDF$$P50$$Gwiley$$H</linktopdf><linktohtml>$$Uhttps://onlinelibrary.wiley.com/doi/full/10.1097%2FMPG.0b013e3182470249$$EHTML$$P50$$Gwiley$$H</linktohtml><link.rule.ids>314,776,780,1411,27903,27904,45553,45554</link.rule.ids><backlink>$$Uhttp://pascal-francis.inist.fr/vibad/index.php?action=getRecordDetail&amp;idt=26050181$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22197946$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Alessio, Maria G.</creatorcontrib><creatorcontrib>Tonutti, Elio</creatorcontrib><creatorcontrib>Brusca, Ignazio</creatorcontrib><creatorcontrib>Radice, Antonella</creatorcontrib><creatorcontrib>Licini, Lisa</creatorcontrib><creatorcontrib>Sonzogni, Aurelio</creatorcontrib><creatorcontrib>Florena, Ada</creatorcontrib><creatorcontrib>Schiaffino, Eugenio</creatorcontrib><creatorcontrib>Marus, Wally</creatorcontrib><creatorcontrib>Sulfaro, Sandro</creatorcontrib><creatorcontrib>Villalta, Danilo</creatorcontrib><creatorcontrib>Study Group on Autoimmune Diseases of Italian Society of Laboratory Medicine</creatorcontrib><creatorcontrib>Study Group on Autoimmune Diseases of the Italian Society of Laboratory Medicine</creatorcontrib><title>Correlation Between IgA Tissue Transglutaminase Antibody Ratio and Histological Finding in Celiac Disease</title><title>Journal of pediatric gastroenterology and nutrition</title><addtitle>J Pediatr Gastroenterol Nutr</addtitle><description>ABSTRACT Objectives: Positivity of both immumoglobulin A anti‐tissue transglutaminase (TTG) and anti‐endomysium antibodies (EMA) has a positive predictive value of nearly 100% for celiac disease (CD). The objective of the present study was to evaluate whether patients of any age, with high pretest probability of CD and high titre of anti‐TTG and EMA positivity, have a high probability of intestinal damage and may not require the biopsy for final diagnosis. Methods: A retrospective analysis of 412 consecutively referred patients, age range 10 months to 72 years, who underwent small‐bowel biopsy for suspicion of CD and positivity to both anti‐TTG and EMA, was performed at 4 Italian centers. Biopsies were evaluated independently by 2 pathologists using Marsh modified classification; in cases of dissimilar results, a third pathologist examined the biopsy. The final histological finding diagnosis was expressed as the prevalent or highest score assigned by the pathologist board. Results: Three hundred ninety‐six patients (96.1%) had histological findings consistent with CD (grade 2 and 3a, 3b, or 3c of modified Marsh classification). An anti‐TTG ratio ≥7 was able to identify with the 3 assays used (Celikey, anti‐TTG immumoglobulin A, EuTTG) all of the patients with significant mucosal damage (Marsh ≥2) independent of age and sex; specificity and positive predictive value were 100%. An anti‐TTG ratio &gt;20 was more specific (99.8%) for identification of patients with villous atrophy (Marsh 3 a, b, or c). Conclusions: Patients with positivity of anti‐TTG ≥7‐fold cutoff, confirmed by positivity to EMA, have a high‐degree probability of duodenal damage. In selected conditions, a duodenal biopsy may be avoided and a confirmed greatly positive anti‐TTG result could be the basis to prescribe a gluten‐free diet.</description><subject>Adolescent</subject><subject>Adult</subject><subject>Aged</subject><subject>anti‐TTG ratio</subject><subject>Biological and medical sciences</subject><subject>Biopsy</subject><subject>celiac disease</subject><subject>Celiac Disease - classification</subject><subject>Celiac Disease - immunology</subject><subject>Celiac Disease - pathology</subject><subject>Child</subject><subject>Child, Preschool</subject><subject>Duodenum - pathology</subject><subject>Feeding. Feeding behavior</subject><subject>Female</subject><subject>Fundamental and applied biological sciences. Psychology</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>GTP-Binding Proteins - immunology</subject><subject>Humans</subject><subject>Immunoglobulin A - blood</subject><subject>Infant</subject><subject>Logistic Models</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>mucosal damage</subject><subject>Muscles - immunology</subject><subject>Other diseases. Semiology</subject><subject>Predictive Value of Tests</subject><subject>Retrospective Studies</subject><subject>Severity of Illness Index</subject><subject>Statistics, Nonparametric</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Transglutaminases - immunology</subject><subject>Vertebrates: anatomy and physiology, studies on body, several organs or systems</subject><subject>Young Adult</subject><issn>0277-2116</issn><issn>1536-4801</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><sourceid>EIF</sourceid><recordid>eNqNkMFuEzEQQC0EoqHwBwj5gsRly3jttb0HDmkgbVGBCoXzyrFnU4PjLfauovw9LgkgcYGLfXnPnnmEPGdwxqBVrz_cXJzBGhhHznQtFNSifUBmrOGyEhrYQzKDWqmqZkyekCc5fwUAJRp4TE7qmrWqFXJG_GJICYMZ_RDpOY47xEivNnO68jlPSFfJxLwJ02i2PpqMdB5Hvx7cnn6-d6iJjl76PA5h2HhrAl366HzcUB_pAoM3lr71GYv5lDzqTcj47Hifki_Ld6vFZXX96eJqMb-urNCyrbRZS6Z0zXrnGGjLuRKit-WwTjoE7TT0yLQQArlrpdJamrK-bRrgqpX8lLw6vHuXhu8T5rHb-mwxBBNxmHLHgNe6VeInKg6oTUPOCfvuLvmtSfsCdfeRuxK5-zty0V4cf5jWW3S_pV9VC_DyCJhcmvSlofX5DyehAaZZ4fSB2w1hxJS_hWmHqbtFE8bbf83w5qj6gPv_mrt7f_ORny9BMqn5D_P1qAg</recordid><startdate>201207</startdate><enddate>201207</enddate><creator>Alessio, Maria G.</creator><creator>Tonutti, Elio</creator><creator>Brusca, Ignazio</creator><creator>Radice, Antonella</creator><creator>Licini, Lisa</creator><creator>Sonzogni, Aurelio</creator><creator>Florena, Ada</creator><creator>Schiaffino, Eugenio</creator><creator>Marus, Wally</creator><creator>Sulfaro, Sandro</creator><creator>Villalta, Danilo</creator><general>Copyright by ESPGHAN and NASPGHAN</general><general>Lippincott Williams &amp; 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>201207</creationdate><title>Correlation Between IgA Tissue Transglutaminase Antibody Ratio and Histological Finding in Celiac Disease</title><author>Alessio, Maria G. ; Tonutti, Elio ; Brusca, Ignazio ; Radice, Antonella ; Licini, Lisa ; Sonzogni, Aurelio ; Florena, Ada ; Schiaffino, Eugenio ; Marus, Wally ; Sulfaro, Sandro ; Villalta, Danilo</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c4869-8ab617821fdd108c33744fc744cd6de08d80fe18444e3d967886a247c55037963</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adolescent</topic><topic>Adult</topic><topic>Aged</topic><topic>anti‐TTG ratio</topic><topic>Biological and medical sciences</topic><topic>Biopsy</topic><topic>celiac disease</topic><topic>Celiac Disease - classification</topic><topic>Celiac Disease - immunology</topic><topic>Celiac Disease - pathology</topic><topic>Child</topic><topic>Child, Preschool</topic><topic>Duodenum - pathology</topic><topic>Feeding. Feeding behavior</topic><topic>Female</topic><topic>Fundamental and applied biological sciences. Psychology</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>GTP-Binding Proteins - immunology</topic><topic>Humans</topic><topic>Immunoglobulin A - blood</topic><topic>Infant</topic><topic>Logistic Models</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>mucosal damage</topic><topic>Muscles - immunology</topic><topic>Other diseases. Semiology</topic><topic>Predictive Value of Tests</topic><topic>Retrospective Studies</topic><topic>Severity of Illness Index</topic><topic>Statistics, Nonparametric</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Transglutaminases - immunology</topic><topic>Vertebrates: anatomy and physiology, studies on body, several organs or systems</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Alessio, Maria G.</creatorcontrib><creatorcontrib>Tonutti, Elio</creatorcontrib><creatorcontrib>Brusca, Ignazio</creatorcontrib><creatorcontrib>Radice, Antonella</creatorcontrib><creatorcontrib>Licini, Lisa</creatorcontrib><creatorcontrib>Sonzogni, Aurelio</creatorcontrib><creatorcontrib>Florena, Ada</creatorcontrib><creatorcontrib>Schiaffino, Eugenio</creatorcontrib><creatorcontrib>Marus, Wally</creatorcontrib><creatorcontrib>Sulfaro, Sandro</creatorcontrib><creatorcontrib>Villalta, Danilo</creatorcontrib><creatorcontrib>Study Group on Autoimmune Diseases of Italian Society of Laboratory Medicine</creatorcontrib><creatorcontrib>Study Group on Autoimmune Diseases of the Italian Society of Laboratory Medicine</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>Journal of pediatric gastroenterology and nutrition</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Alessio, Maria G.</au><au>Tonutti, Elio</au><au>Brusca, Ignazio</au><au>Radice, Antonella</au><au>Licini, Lisa</au><au>Sonzogni, Aurelio</au><au>Florena, Ada</au><au>Schiaffino, Eugenio</au><au>Marus, Wally</au><au>Sulfaro, Sandro</au><au>Villalta, Danilo</au><aucorp>Study Group on Autoimmune Diseases of Italian Society of Laboratory Medicine</aucorp><aucorp>Study Group on Autoimmune Diseases of the Italian Society of Laboratory Medicine</aucorp><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Correlation Between IgA Tissue Transglutaminase Antibody Ratio and Histological Finding in Celiac Disease</atitle><jtitle>Journal of pediatric gastroenterology and nutrition</jtitle><addtitle>J Pediatr Gastroenterol Nutr</addtitle><date>2012-07</date><risdate>2012</risdate><volume>55</volume><issue>1</issue><spage>44</spage><epage>49</epage><pages>44-49</pages><issn>0277-2116</issn><eissn>1536-4801</eissn><coden>JPGND6</coden><abstract>ABSTRACT Objectives: Positivity of both immumoglobulin A anti‐tissue transglutaminase (TTG) and anti‐endomysium antibodies (EMA) has a positive predictive value of nearly 100% for celiac disease (CD). The objective of the present study was to evaluate whether patients of any age, with high pretest probability of CD and high titre of anti‐TTG and EMA positivity, have a high probability of intestinal damage and may not require the biopsy for final diagnosis. Methods: A retrospective analysis of 412 consecutively referred patients, age range 10 months to 72 years, who underwent small‐bowel biopsy for suspicion of CD and positivity to both anti‐TTG and EMA, was performed at 4 Italian centers. Biopsies were evaluated independently by 2 pathologists using Marsh modified classification; in cases of dissimilar results, a third pathologist examined the biopsy. The final histological finding diagnosis was expressed as the prevalent or highest score assigned by the pathologist board. Results: Three hundred ninety‐six patients (96.1%) had histological findings consistent with CD (grade 2 and 3a, 3b, or 3c of modified Marsh classification). An anti‐TTG ratio ≥7 was able to identify with the 3 assays used (Celikey, anti‐TTG immumoglobulin A, EuTTG) all of the patients with significant mucosal damage (Marsh ≥2) independent of age and sex; specificity and positive predictive value were 100%. An anti‐TTG ratio &gt;20 was more specific (99.8%) for identification of patients with villous atrophy (Marsh 3 a, b, or c). Conclusions: Patients with positivity of anti‐TTG ≥7‐fold cutoff, confirmed by positivity to EMA, have a high‐degree probability of duodenal damage. In selected conditions, a duodenal biopsy may be avoided and a confirmed greatly positive anti‐TTG result could be the basis to prescribe a gluten‐free diet.</abstract><cop>Hagerstown, MD</cop><pub>Copyright by ESPGHAN and NASPGHAN</pub><pmid>22197946</pmid><doi>10.1097/MPG.0b013e3182470249</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record>
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subjects Adolescent
Adult
Aged
anti‐TTG ratio
Biological and medical sciences
Biopsy
celiac disease
Celiac Disease - classification
Celiac Disease - immunology
Celiac Disease - pathology
Child
Child, Preschool
Duodenum - pathology
Feeding. Feeding behavior
Female
Fundamental and applied biological sciences. Psychology
Gastroenterology. Liver. Pancreas. Abdomen
GTP-Binding Proteins - immunology
Humans
Immunoglobulin A - blood
Infant
Logistic Models
Male
Medical sciences
Middle Aged
mucosal damage
Muscles - immunology
Other diseases. Semiology
Predictive Value of Tests
Retrospective Studies
Severity of Illness Index
Statistics, Nonparametric
Stomach. Duodenum. Small intestine. Colon. Rectum. Anus
Transglutaminases - immunology
Vertebrates: anatomy and physiology, studies on body, several organs or systems
Young Adult
title Correlation Between IgA Tissue Transglutaminase Antibody Ratio and Histological Finding in Celiac Disease
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