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Fecal calprotectin and S100A12 have low utility in prediction of small bowel Crohn's disease detected by wireless capsule endoscopy
Abstract Objective. Data on fecal calprotectin and S100A12 in predicting wireless capsule endoscopy (WCE) findings in suspicion of Crohn's disease (CD) are scarce. Our aim was to study the role of calprotectin and S100A12 in predicting inflammatory lesions of small bowel in patients undergoing...
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Published in: | Scandinavian journal of gastroenterology 2012-07, Vol.47 (7), p.778-784 |
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container_title | Scandinavian journal of gastroenterology |
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creator | Sipponen, Taina Haapamäki, Johanna Savilahti, Erkki Alfthan, Henrik Hämäläinen, Esa Rautiainen, Henna Koskenpato, Jari Nuutinen, Hannu Färkkilä, Martti |
description | Abstract
Objective.
Data on fecal calprotectin and S100A12 in predicting wireless capsule endoscopy (WCE) findings in suspicion of Crohn's disease (CD) are scarce. Our aim was to study the role of calprotectin and S100A12 in predicting inflammatory lesions of small bowel in patients undergoing WCE.
Material and methods.
84 patients undergoing WCE (77 for suspicion of CD and 7 CD patients for evaluation of disease extent) were prospectively recruited. WCE findings were scored. Patients provided a stool sample for measurements of biomarkers. Patients underwent an esophagogastroduodenoscopy and ileocolonoscopy before WCE.
Results.
WCE was abnormal in 35 (42%) of 84 patients: 14 patients with CD, 8 with NSAID enteropathies, 8 with angioectasias, 4 with polyps or tumors, and 1 with ischemic stricture. Median calprotectin concentration in the study population was 22 μg/g (range 2-342) and S100A12 concentration 0.048 μg/g (range 0.003-1.215). Fecal calprotectin was significantly higher in CD patients (median 91, range 2-312) compared with those with normal WCE or other abnormalities (p = 0.008), whereas fecal S100A12 (0.087 μg/g, range 0.008-0.896) did not differ between the groups (p = 0.166). In detecting inflammatory small bowel lesions, sensitivity, specificity, positive predictive value, and negative predictive value for fecal calprotectin (cutoff 50 μg/g) were 59%, 71%, 42%, and 83%, and for S100A12 (cutoff 0.06 μg/g) these were 59%, 66%, 38%, and 82%.
Conclusions.
In predicting small bowel inflammatory changes, fecal biomarkers calprotectin and S100A12 have moderate specificity, but low sensitivity. Neither fecal calprotectin nor S100A12 can be used for screening or excluding small bowel CD. |
doi_str_mv | 10.3109/00365521.2012.677953 |
format | article |
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Objective.
Data on fecal calprotectin and S100A12 in predicting wireless capsule endoscopy (WCE) findings in suspicion of Crohn's disease (CD) are scarce. Our aim was to study the role of calprotectin and S100A12 in predicting inflammatory lesions of small bowel in patients undergoing WCE.
Material and methods.
84 patients undergoing WCE (77 for suspicion of CD and 7 CD patients for evaluation of disease extent) were prospectively recruited. WCE findings were scored. Patients provided a stool sample for measurements of biomarkers. Patients underwent an esophagogastroduodenoscopy and ileocolonoscopy before WCE.
Results.
WCE was abnormal in 35 (42%) of 84 patients: 14 patients with CD, 8 with NSAID enteropathies, 8 with angioectasias, 4 with polyps or tumors, and 1 with ischemic stricture. Median calprotectin concentration in the study population was 22 μg/g (range 2-342) and S100A12 concentration 0.048 μg/g (range 0.003-1.215). Fecal calprotectin was significantly higher in CD patients (median 91, range 2-312) compared with those with normal WCE or other abnormalities (p = 0.008), whereas fecal S100A12 (0.087 μg/g, range 0.008-0.896) did not differ between the groups (p = 0.166). In detecting inflammatory small bowel lesions, sensitivity, specificity, positive predictive value, and negative predictive value for fecal calprotectin (cutoff 50 μg/g) were 59%, 71%, 42%, and 83%, and for S100A12 (cutoff 0.06 μg/g) these were 59%, 66%, 38%, and 82%.
Conclusions.
In predicting small bowel inflammatory changes, fecal biomarkers calprotectin and S100A12 have moderate specificity, but low sensitivity. Neither fecal calprotectin nor S100A12 can be used for screening or excluding small bowel CD.</description><identifier>ISSN: 0036-5521</identifier><identifier>EISSN: 1502-7708</identifier><identifier>DOI: 10.3109/00365521.2012.677953</identifier><identifier>PMID: 22519419</identifier><identifier>CODEN: SJGRA4</identifier><language>eng</language><publisher>Colchester: Informa Healthcare</publisher><subject>Adult ; Aged ; Area Under Curve ; Biological and medical sciences ; biomarkers ; Biomarkers - analysis ; Capsule Endoscopy ; Crohn Disease - diagnosis ; Crohn Disease - pathology ; Crohn's disease activity ; Digestive system. Abdomen ; Endoscopy ; fecal markers ; Feces - chemistry ; Female ; Gastroenterology. Liver. Pancreas. Abdomen ; Humans ; IBD ; Intestine, Small - pathology ; Investigative techniques, diagnostic techniques (general aspects) ; Leukocyte L1 Antigen Complex - analysis ; Male ; Medical sciences ; Middle Aged ; Other diseases. Semiology ; Predictive Value of Tests ; ROC Curve ; S100 Proteins - analysis ; S100A12 Protein ; small intestine ; Statistics, Nonparametric ; Stomach. Duodenum. Small intestine. Colon. Rectum. Anus ; Young Adult</subject><ispartof>Scandinavian journal of gastroenterology, 2012-07, Vol.47 (7), p.778-784</ispartof><rights>Informa Healthcare 2012</rights><rights>2015 INIST-CNRS</rights><lds50>peer_reviewed</lds50><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c448t-8cc50e8931c0f9cd86fe00e930326930ebc685334241da0749c0278fda5d3a5b3</citedby><cites>FETCH-LOGICAL-c448t-8cc50e8931c0f9cd86fe00e930326930ebc685334241da0749c0278fda5d3a5b3</cites></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=26042532$$DView record in Pascal Francis$$Hfree_for_read</backlink><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/22519419$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Sipponen, Taina</creatorcontrib><creatorcontrib>Haapamäki, Johanna</creatorcontrib><creatorcontrib>Savilahti, Erkki</creatorcontrib><creatorcontrib>Alfthan, Henrik</creatorcontrib><creatorcontrib>Hämäläinen, Esa</creatorcontrib><creatorcontrib>Rautiainen, Henna</creatorcontrib><creatorcontrib>Koskenpato, Jari</creatorcontrib><creatorcontrib>Nuutinen, Hannu</creatorcontrib><creatorcontrib>Färkkilä, Martti</creatorcontrib><title>Fecal calprotectin and S100A12 have low utility in prediction of small bowel Crohn's disease detected by wireless capsule endoscopy</title><title>Scandinavian journal of gastroenterology</title><addtitle>Scand J Gastroenterol</addtitle><description>Abstract
Objective.
Data on fecal calprotectin and S100A12 in predicting wireless capsule endoscopy (WCE) findings in suspicion of Crohn's disease (CD) are scarce. Our aim was to study the role of calprotectin and S100A12 in predicting inflammatory lesions of small bowel in patients undergoing WCE.
Material and methods.
84 patients undergoing WCE (77 for suspicion of CD and 7 CD patients for evaluation of disease extent) were prospectively recruited. WCE findings were scored. Patients provided a stool sample for measurements of biomarkers. Patients underwent an esophagogastroduodenoscopy and ileocolonoscopy before WCE.
Results.
WCE was abnormal in 35 (42%) of 84 patients: 14 patients with CD, 8 with NSAID enteropathies, 8 with angioectasias, 4 with polyps or tumors, and 1 with ischemic stricture. Median calprotectin concentration in the study population was 22 μg/g (range 2-342) and S100A12 concentration 0.048 μg/g (range 0.003-1.215). Fecal calprotectin was significantly higher in CD patients (median 91, range 2-312) compared with those with normal WCE or other abnormalities (p = 0.008), whereas fecal S100A12 (0.087 μg/g, range 0.008-0.896) did not differ between the groups (p = 0.166). In detecting inflammatory small bowel lesions, sensitivity, specificity, positive predictive value, and negative predictive value for fecal calprotectin (cutoff 50 μg/g) were 59%, 71%, 42%, and 83%, and for S100A12 (cutoff 0.06 μg/g) these were 59%, 66%, 38%, and 82%.
Conclusions.
In predicting small bowel inflammatory changes, fecal biomarkers calprotectin and S100A12 have moderate specificity, but low sensitivity. Neither fecal calprotectin nor S100A12 can be used for screening or excluding small bowel CD.</description><subject>Adult</subject><subject>Aged</subject><subject>Area Under Curve</subject><subject>Biological and medical sciences</subject><subject>biomarkers</subject><subject>Biomarkers - analysis</subject><subject>Capsule Endoscopy</subject><subject>Crohn Disease - diagnosis</subject><subject>Crohn Disease - pathology</subject><subject>Crohn's disease activity</subject><subject>Digestive system. Abdomen</subject><subject>Endoscopy</subject><subject>fecal markers</subject><subject>Feces - chemistry</subject><subject>Female</subject><subject>Gastroenterology. Liver. Pancreas. Abdomen</subject><subject>Humans</subject><subject>IBD</subject><subject>Intestine, Small - pathology</subject><subject>Investigative techniques, diagnostic techniques (general aspects)</subject><subject>Leukocyte L1 Antigen Complex - analysis</subject><subject>Male</subject><subject>Medical sciences</subject><subject>Middle Aged</subject><subject>Other diseases. Semiology</subject><subject>Predictive Value of Tests</subject><subject>ROC Curve</subject><subject>S100 Proteins - analysis</subject><subject>S100A12 Protein</subject><subject>small intestine</subject><subject>Statistics, Nonparametric</subject><subject>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</subject><subject>Young Adult</subject><issn>0036-5521</issn><issn>1502-7708</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2012</creationdate><recordtype>article</recordtype><recordid>eNqFkEtv1DAURi0EokPhHyDkDYJNptd2nMcGVI0oVKrEorCOHPtG48qJg50wypo_jqOZAbGhC9sLn_v4DiGvGWwFg_oKQBRScrblwPi2KMtaiidkwyTwrCyheko2K5KtzAV5EeMDAMgyr5-TC84lq3NWb8ivG9TK0XTG4CfUkx2oGgy9ZwDXjNO9-onU-QOdJ-vstND0PwY0NpF-oL6jsVfO0dYf0NFd8PvhXaTGRlQRqcG1JRraLvRgAzqMMc0a4-yQ4mB81H5cXpJnnXIRX53eS_L95tO33Zfs7uvn2931XabzvJqySmsJWNWCaehqbaqiQwCsBQhepBtbXVRSiJznzChISTXwsuqMkkYo2YpL8v7YN0X9MWOcmt5Gjc6pAf0cGwasLlhZVCKh-RHVwccYsGvGYHsVlgQ1q_7mrL9Z9TdH_anszWnC3PZo_hSdfSfg7QlQMTnvghq0jX-5AnIuBU_cxyNnh86HXh18cKaZ1OJ8OBeJR1b58E-HPSo37bUK2Dz4OQxJ9P-z_AY7q7R5</recordid><startdate>20120701</startdate><enddate>20120701</enddate><creator>Sipponen, Taina</creator><creator>Haapamäki, Johanna</creator><creator>Savilahti, Erkki</creator><creator>Alfthan, Henrik</creator><creator>Hämäläinen, Esa</creator><creator>Rautiainen, Henna</creator><creator>Koskenpato, Jari</creator><creator>Nuutinen, Hannu</creator><creator>Färkkilä, Martti</creator><general>Informa Healthcare</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></search><sort><creationdate>20120701</creationdate><title>Fecal calprotectin and S100A12 have low utility in prediction of small bowel Crohn's disease detected by wireless capsule endoscopy</title><author>Sipponen, Taina ; Haapamäki, Johanna ; Savilahti, Erkki ; Alfthan, Henrik ; Hämäläinen, Esa ; Rautiainen, Henna ; Koskenpato, Jari ; Nuutinen, Hannu ; Färkkilä, Martti</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c448t-8cc50e8931c0f9cd86fe00e930326930ebc685334241da0749c0278fda5d3a5b3</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2012</creationdate><topic>Adult</topic><topic>Aged</topic><topic>Area Under Curve</topic><topic>Biological and medical sciences</topic><topic>biomarkers</topic><topic>Biomarkers - analysis</topic><topic>Capsule Endoscopy</topic><topic>Crohn Disease - diagnosis</topic><topic>Crohn Disease - pathology</topic><topic>Crohn's disease activity</topic><topic>Digestive system. Abdomen</topic><topic>Endoscopy</topic><topic>fecal markers</topic><topic>Feces - chemistry</topic><topic>Female</topic><topic>Gastroenterology. Liver. Pancreas. Abdomen</topic><topic>Humans</topic><topic>IBD</topic><topic>Intestine, Small - pathology</topic><topic>Investigative techniques, diagnostic techniques (general aspects)</topic><topic>Leukocyte L1 Antigen Complex - analysis</topic><topic>Male</topic><topic>Medical sciences</topic><topic>Middle Aged</topic><topic>Other diseases. Semiology</topic><topic>Predictive Value of Tests</topic><topic>ROC Curve</topic><topic>S100 Proteins - analysis</topic><topic>S100A12 Protein</topic><topic>small intestine</topic><topic>Statistics, Nonparametric</topic><topic>Stomach. Duodenum. Small intestine. Colon. Rectum. Anus</topic><topic>Young Adult</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Sipponen, Taina</creatorcontrib><creatorcontrib>Haapamäki, Johanna</creatorcontrib><creatorcontrib>Savilahti, Erkki</creatorcontrib><creatorcontrib>Alfthan, Henrik</creatorcontrib><creatorcontrib>Hämäläinen, Esa</creatorcontrib><creatorcontrib>Rautiainen, Henna</creatorcontrib><creatorcontrib>Koskenpato, Jari</creatorcontrib><creatorcontrib>Nuutinen, Hannu</creatorcontrib><creatorcontrib>Färkkilä, Martti</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>Scandinavian journal of gastroenterology</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Sipponen, Taina</au><au>Haapamäki, Johanna</au><au>Savilahti, Erkki</au><au>Alfthan, Henrik</au><au>Hämäläinen, Esa</au><au>Rautiainen, Henna</au><au>Koskenpato, Jari</au><au>Nuutinen, Hannu</au><au>Färkkilä, Martti</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Fecal calprotectin and S100A12 have low utility in prediction of small bowel Crohn's disease detected by wireless capsule endoscopy</atitle><jtitle>Scandinavian journal of gastroenterology</jtitle><addtitle>Scand J Gastroenterol</addtitle><date>2012-07-01</date><risdate>2012</risdate><volume>47</volume><issue>7</issue><spage>778</spage><epage>784</epage><pages>778-784</pages><issn>0036-5521</issn><eissn>1502-7708</eissn><coden>SJGRA4</coden><abstract>Abstract
Objective.
Data on fecal calprotectin and S100A12 in predicting wireless capsule endoscopy (WCE) findings in suspicion of Crohn's disease (CD) are scarce. Our aim was to study the role of calprotectin and S100A12 in predicting inflammatory lesions of small bowel in patients undergoing WCE.
Material and methods.
84 patients undergoing WCE (77 for suspicion of CD and 7 CD patients for evaluation of disease extent) were prospectively recruited. WCE findings were scored. Patients provided a stool sample for measurements of biomarkers. Patients underwent an esophagogastroduodenoscopy and ileocolonoscopy before WCE.
Results.
WCE was abnormal in 35 (42%) of 84 patients: 14 patients with CD, 8 with NSAID enteropathies, 8 with angioectasias, 4 with polyps or tumors, and 1 with ischemic stricture. Median calprotectin concentration in the study population was 22 μg/g (range 2-342) and S100A12 concentration 0.048 μg/g (range 0.003-1.215). Fecal calprotectin was significantly higher in CD patients (median 91, range 2-312) compared with those with normal WCE or other abnormalities (p = 0.008), whereas fecal S100A12 (0.087 μg/g, range 0.008-0.896) did not differ between the groups (p = 0.166). In detecting inflammatory small bowel lesions, sensitivity, specificity, positive predictive value, and negative predictive value for fecal calprotectin (cutoff 50 μg/g) were 59%, 71%, 42%, and 83%, and for S100A12 (cutoff 0.06 μg/g) these were 59%, 66%, 38%, and 82%.
Conclusions.
In predicting small bowel inflammatory changes, fecal biomarkers calprotectin and S100A12 have moderate specificity, but low sensitivity. Neither fecal calprotectin nor S100A12 can be used for screening or excluding small bowel CD.</abstract><cop>Colchester</cop><pub>Informa Healthcare</pub><pmid>22519419</pmid><doi>10.3109/00365521.2012.677953</doi><tpages>7</tpages></addata></record> |
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subjects | Adult Aged Area Under Curve Biological and medical sciences biomarkers Biomarkers - analysis Capsule Endoscopy Crohn Disease - diagnosis Crohn Disease - pathology Crohn's disease activity Digestive system. Abdomen Endoscopy fecal markers Feces - chemistry Female Gastroenterology. Liver. Pancreas. Abdomen Humans IBD Intestine, Small - pathology Investigative techniques, diagnostic techniques (general aspects) Leukocyte L1 Antigen Complex - analysis Male Medical sciences Middle Aged Other diseases. Semiology Predictive Value of Tests ROC Curve S100 Proteins - analysis S100A12 Protein small intestine Statistics, Nonparametric Stomach. Duodenum. Small intestine. Colon. Rectum. Anus Young Adult |
title | Fecal calprotectin and S100A12 have low utility in prediction of small bowel Crohn's disease detected by wireless capsule endoscopy |
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