The prospective use of cytokine markers for inflammatory bowel disease evaluation
Stool is stable at room temperature, resistant to multiple freezing and thawing cycles, and easily processable. Some stool metabolites have approved quantitative point of care test kits.14 Fecal calprotectin Calprotectin is released by neutrophils at an inflamed site, so fecal measurement of calprot...
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description | Stool is stable at room temperature, resistant to multiple freezing and thawing cycles, and easily processable. Some stool metabolites have approved quantitative point of care test kits.14 Fecal calprotectin Calprotectin is released by neutrophils at an inflamed site, so fecal measurement of calprotectin is an indirect measurement of neutrophil infiltration of the gastrointestinal tract.15 CD stool specimens have four times the mean fecal calprotectin (FC) compared to the healthy stool; high FC is associated with reduced microbial diversity in severely inflamed patients.9 FC can detect lower inflammatory activity better than CRP and can distinguish between active versus quiescent IBD and IBD versus irritable bowel syndrome (IBS).16 Compared to all other noninvasive procedures, FC dominates with a 64% to 95% sensitivity and a 79% to 93% specificity.17 Furthermore, unlike CRP, FC can grade the severity of most IBD subtypes. Fecal lactoferrin Changes in fecal lactoferrin (FL) levels are proportional with leukocyte margination and diapedesis into the gut mucosa and exhibit a close correlation with inflammatory endoscopic and histological activity.19, 20 Comparable to histologic analysis, FL was reported to increase within 2 months of pouchitis development. Furthermore, the distinctive fecal microbial signatures of all IBD subtypes need to be mapped in the future.26 Autoantibodies The presence of autoantibodies suggests a loss of tolerance to commensal bacteria. [...]the reduction of intestinal bacteria in IBD affects the proper development of gut immune tolerance.5 Antineutrophil Cytoplasmic Antibody Antineutrophil cytoplasmic antibody (ANCA) is categorized based on two staining patterns: cytoplasmic ANCA and peripheral ANCA (pANCA).27 26.19% of CD and 66.05% of UC individuals are ANCA positive which show that not all IBD cases will produce ANCA.28 A positive pANCA test has an 86% specificity to UC patients and 66% specificity to CD patients, suggesting that pANCA is a poor IBD screening test but a strong UC discriminator.29 Although ANCA is a potent UC discriminator, no evidence suggests that ANCA can pinpoint the location of inflammatory involvement nor can pANCA predict postoperative relapse, proving this marker to be inferior to endoscopy.29, 30 Anti-Saccharomyces cerevisiae antibody Anti-Saccharomyces cerevisiae Antibody (ASCA) was initially discovered to target the cell wall of Saccharomyces cerevisiae, but it is now observed in some instances of IBD. |
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Some stool metabolites have approved quantitative point of care test kits.14 Fecal calprotectin Calprotectin is released by neutrophils at an inflamed site, so fecal measurement of calprotectin is an indirect measurement of neutrophil infiltration of the gastrointestinal tract.15 CD stool specimens have four times the mean fecal calprotectin (FC) compared to the healthy stool; high FC is associated with reduced microbial diversity in severely inflamed patients.9 FC can detect lower inflammatory activity better than CRP and can distinguish between active versus quiescent IBD and IBD versus irritable bowel syndrome (IBS).16 Compared to all other noninvasive procedures, FC dominates with a 64% to 95% sensitivity and a 79% to 93% specificity.17 Furthermore, unlike CRP, FC can grade the severity of most IBD subtypes. Fecal lactoferrin Changes in fecal lactoferrin (FL) levels are proportional with leukocyte margination and diapedesis into the gut mucosa and exhibit a close correlation with inflammatory endoscopic and histological activity.19, 20 Comparable to histologic analysis, FL was reported to increase within 2 months of pouchitis development. Furthermore, the distinctive fecal microbial signatures of all IBD subtypes need to be mapped in the future.26 Autoantibodies The presence of autoantibodies suggests a loss of tolerance to commensal bacteria. [...]the reduction of intestinal bacteria in IBD affects the proper development of gut immune tolerance.5 Antineutrophil Cytoplasmic Antibody Antineutrophil cytoplasmic antibody (ANCA) is categorized based on two staining patterns: cytoplasmic ANCA and peripheral ANCA (pANCA).27 26.19% of CD and 66.05% of UC individuals are ANCA positive which show that not all IBD cases will produce ANCA.28 A positive pANCA test has an 86% specificity to UC patients and 66% specificity to CD patients, suggesting that pANCA is a poor IBD screening test but a strong UC discriminator.29 Although ANCA is a potent UC discriminator, no evidence suggests that ANCA can pinpoint the location of inflammatory involvement nor can pANCA predict postoperative relapse, proving this marker to be inferior to endoscopy.29, 30 Anti-Saccharomyces cerevisiae antibody Anti-Saccharomyces cerevisiae Antibody (ASCA) was initially discovered to target the cell wall of Saccharomyces cerevisiae, but it is now observed in some instances of IBD.</description><identifier>ISSN: 0580-7247</identifier><identifier>EISSN: 2771-6759</identifier><language>eng</language><publisher>Nashville: Endeavor Business Media</publisher><subject>Analysis ; Antibodies ; Antigens ; Bacteria ; Biological markers ; Biomarkers ; Crohn's disease ; Cytokines ; Diagnosis ; Endoscopy ; Feces ; Health aspects ; Immune system ; Inflammation ; Inflammatory bowel disease ; Inflammatory bowel diseases ; Inflammatory diseases ; Irritable bowel syndrome ; Metabolites ; Microbiota ; Patients ; Permeability ; Remission (Medicine) ; Yeast</subject><ispartof>MLO. Medical laboratory observer, 2022-07, Vol.54 (7), p.10-20</ispartof><rights>COPYRIGHT 2022 Endeavor Business Media</rights><rights>Copyright Endeavor Business Media Jul 2022</rights><woscitedreferencessubscribed>false</woscitedreferencessubscribed></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><link.rule.ids>312,777,781,788</link.rule.ids></links><search><creatorcontrib>Reyes, Dioco Dioel</creatorcontrib><creatorcontrib>Shokrani, Masih</creatorcontrib><title>The prospective use of cytokine markers for inflammatory bowel disease evaluation</title><title>MLO. Medical laboratory observer</title><addtitle>Medical Laboratory Observer</addtitle><description>Stool is stable at room temperature, resistant to multiple freezing and thawing cycles, and easily processable. Some stool metabolites have approved quantitative point of care test kits.14 Fecal calprotectin Calprotectin is released by neutrophils at an inflamed site, so fecal measurement of calprotectin is an indirect measurement of neutrophil infiltration of the gastrointestinal tract.15 CD stool specimens have four times the mean fecal calprotectin (FC) compared to the healthy stool; high FC is associated with reduced microbial diversity in severely inflamed patients.9 FC can detect lower inflammatory activity better than CRP and can distinguish between active versus quiescent IBD and IBD versus irritable bowel syndrome (IBS).16 Compared to all other noninvasive procedures, FC dominates with a 64% to 95% sensitivity and a 79% to 93% specificity.17 Furthermore, unlike CRP, FC can grade the severity of most IBD subtypes. Fecal lactoferrin Changes in fecal lactoferrin (FL) levels are proportional with leukocyte margination and diapedesis into the gut mucosa and exhibit a close correlation with inflammatory endoscopic and histological activity.19, 20 Comparable to histologic analysis, FL was reported to increase within 2 months of pouchitis development. Furthermore, the distinctive fecal microbial signatures of all IBD subtypes need to be mapped in the future.26 Autoantibodies The presence of autoantibodies suggests a loss of tolerance to commensal bacteria. [...]the reduction of intestinal bacteria in IBD affects the proper development of gut immune tolerance.5 Antineutrophil Cytoplasmic Antibody Antineutrophil cytoplasmic antibody (ANCA) is categorized based on two staining patterns: cytoplasmic ANCA and peripheral ANCA (pANCA).27 26.19% of CD and 66.05% of UC individuals are ANCA positive which show that not all IBD cases will produce ANCA.28 A positive pANCA test has an 86% specificity to UC patients and 66% specificity to CD patients, suggesting that pANCA is a poor IBD screening test but a strong UC discriminator.29 Although ANCA is a potent UC discriminator, no evidence suggests that ANCA can pinpoint the location of inflammatory involvement nor can pANCA predict postoperative relapse, proving this marker to be inferior to endoscopy.29, 30 Anti-Saccharomyces cerevisiae antibody Anti-Saccharomyces cerevisiae Antibody (ASCA) was initially discovered to target the cell wall of Saccharomyces cerevisiae, but it is now observed in some instances of IBD.</description><subject>Analysis</subject><subject>Antibodies</subject><subject>Antigens</subject><subject>Bacteria</subject><subject>Biological markers</subject><subject>Biomarkers</subject><subject>Crohn's disease</subject><subject>Cytokines</subject><subject>Diagnosis</subject><subject>Endoscopy</subject><subject>Feces</subject><subject>Health aspects</subject><subject>Immune system</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Inflammatory bowel diseases</subject><subject>Inflammatory diseases</subject><subject>Irritable bowel syndrome</subject><subject>Metabolites</subject><subject>Microbiota</subject><subject>Patients</subject><subject>Permeability</subject><subject>Remission (Medicine)</subject><subject>Yeast</subject><issn>0580-7247</issn><issn>2771-6759</issn><fulltext>true</fulltext><rsrctype>magazinearticle</rsrctype><creationdate>2022</creationdate><recordtype>magazinearticle</recordtype><sourceid>N95</sourceid><sourceid>ABUWG</sourceid><sourceid>AFKRA</sourceid><sourceid>BEC</sourceid><sourceid>BENPR</sourceid><sourceid>CCPQU</sourceid><recordid>eNqV0mFr3CAYB_AwOtj1uu8gKwwKy0hMot7LcrS3wrHStX0djD5JbE28-Zhu_fazXF_cwVFWBQX9PfIX_ZDMKOd5yni1OEpmWSWylNOSf0qOER-y2ESVz5Kbux7IxjvcgArmCciEQFxL1HNwj2YEMkj_CB5J6zwxY2vlMMjg_DNp3B-wRBsEGUvgSdpJBuPGk-RjKy3C59d5ntxfXtwtf6Tr69XV8nyddkWZVanmZcN0yUuhF7RlWgpeaKCNKkUuG860yJUSiukYmuWSqjZbtIwyKuJOkdNinnzZnhvT_54AQ-1h43zAmi4oF4yJoorodIs6aaGO-V3wUg0GVX3O8-zFiCKq9IDqYAQvrRuhNXF5z38_4GPXMBh1sOBsryCaAH9DJyfE-ur21zvsz_-2YrV-65KvVjlroYM6vs3yet9_3fE9SBt6dHZ6eWPch992YDNh_DYYBzRdH3CbZYf_A473y50</recordid><startdate>20220701</startdate><enddate>20220701</enddate><creator>Reyes, Dioco Dioel</creator><creator>Shokrani, Masih</creator><general>Endeavor Business Media</general><scope>N95</scope><scope>XI7</scope><scope>8GL</scope><scope>ISN</scope><scope>ISR</scope><scope>3V.</scope><scope>4T-</scope><scope>4U-</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>88E</scope><scope>8AO</scope><scope>8C1</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>BEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>M1P</scope><scope>NAPCQ</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>S0X</scope></search><sort><creationdate>20220701</creationdate><title>The prospective use of cytokine markers for inflammatory bowel disease evaluation</title><author>Reyes, Dioco Dioel ; Shokrani, Masih</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-g3405-d74b6d4748d92f6da873de2bc481ab76d81cc8c6d72461a2cf09f62628d813123</frbrgroupid><rsrctype>magazinearticle</rsrctype><prefilter>magazinearticle</prefilter><language>eng</language><creationdate>2022</creationdate><topic>Analysis</topic><topic>Antibodies</topic><topic>Antigens</topic><topic>Bacteria</topic><topic>Biological markers</topic><topic>Biomarkers</topic><topic>Crohn's disease</topic><topic>Cytokines</topic><topic>Diagnosis</topic><topic>Endoscopy</topic><topic>Feces</topic><topic>Health aspects</topic><topic>Immune system</topic><topic>Inflammation</topic><topic>Inflammatory bowel disease</topic><topic>Inflammatory bowel diseases</topic><topic>Inflammatory diseases</topic><topic>Irritable bowel syndrome</topic><topic>Metabolites</topic><topic>Microbiota</topic><topic>Patients</topic><topic>Permeability</topic><topic>Remission (Medicine)</topic><topic>Yeast</topic><toplevel>online_resources</toplevel><creatorcontrib>Reyes, Dioco Dioel</creatorcontrib><creatorcontrib>Shokrani, Masih</creatorcontrib><collection>Gale Business: Insights</collection><collection>Business Insights: Essentials</collection><collection>Gale In Context: High School</collection><collection>Gale In Context: Canada</collection><collection>Gale In Context: Science</collection><collection>ProQuest Central (Corporate)</collection><collection>Docstoc</collection><collection>University Readers</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>Medical Database (Alumni Edition)</collection><collection>ProQuest Pharma Collection</collection><collection>ProQuest Public Health Database</collection><collection>Hospital Premium Collection</collection><collection>Hospital Premium Collection (Alumni Edition)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni Edition)</collection><collection>ProQuest Central UK/Ireland</collection><collection>eLibrary</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>Health Research Premium Collection</collection><collection>Health Research Premium Collection (Alumni)</collection><collection>ProQuest Health & Medical Complete (Alumni)</collection><collection>Nursing & Allied Health Database (Alumni Edition)</collection><collection>Health & Medical Collection (Alumni Edition)</collection><collection>Medical Database</collection><collection>Nursing & Allied Health Premium</collection><collection>ProQuest One Academic Eastern Edition (DO NOT USE)</collection><collection>ProQuest One Academic</collection><collection>ProQuest One Academic UKI Edition</collection><collection>ProQuest Central China</collection><collection>SIRS Editorial</collection><jtitle>MLO. Medical laboratory observer</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Reyes, Dioco Dioel</au><au>Shokrani, Masih</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>The prospective use of cytokine markers for inflammatory bowel disease evaluation</atitle><jtitle>MLO. Medical laboratory observer</jtitle><addtitle>Medical Laboratory Observer</addtitle><date>2022-07-01</date><risdate>2022</risdate><volume>54</volume><issue>7</issue><spage>10</spage><epage>20</epage><pages>10-20</pages><issn>0580-7247</issn><eissn>2771-6759</eissn><abstract>Stool is stable at room temperature, resistant to multiple freezing and thawing cycles, and easily processable. Some stool metabolites have approved quantitative point of care test kits.14 Fecal calprotectin Calprotectin is released by neutrophils at an inflamed site, so fecal measurement of calprotectin is an indirect measurement of neutrophil infiltration of the gastrointestinal tract.15 CD stool specimens have four times the mean fecal calprotectin (FC) compared to the healthy stool; high FC is associated with reduced microbial diversity in severely inflamed patients.9 FC can detect lower inflammatory activity better than CRP and can distinguish between active versus quiescent IBD and IBD versus irritable bowel syndrome (IBS).16 Compared to all other noninvasive procedures, FC dominates with a 64% to 95% sensitivity and a 79% to 93% specificity.17 Furthermore, unlike CRP, FC can grade the severity of most IBD subtypes. Fecal lactoferrin Changes in fecal lactoferrin (FL) levels are proportional with leukocyte margination and diapedesis into the gut mucosa and exhibit a close correlation with inflammatory endoscopic and histological activity.19, 20 Comparable to histologic analysis, FL was reported to increase within 2 months of pouchitis development. Furthermore, the distinctive fecal microbial signatures of all IBD subtypes need to be mapped in the future.26 Autoantibodies The presence of autoantibodies suggests a loss of tolerance to commensal bacteria. [...]the reduction of intestinal bacteria in IBD affects the proper development of gut immune tolerance.5 Antineutrophil Cytoplasmic Antibody Antineutrophil cytoplasmic antibody (ANCA) is categorized based on two staining patterns: cytoplasmic ANCA and peripheral ANCA (pANCA).27 26.19% of CD and 66.05% of UC individuals are ANCA positive which show that not all IBD cases will produce ANCA.28 A positive pANCA test has an 86% specificity to UC patients and 66% specificity to CD patients, suggesting that pANCA is a poor IBD screening test but a strong UC discriminator.29 Although ANCA is a potent UC discriminator, no evidence suggests that ANCA can pinpoint the location of inflammatory involvement nor can pANCA predict postoperative relapse, proving this marker to be inferior to endoscopy.29, 30 Anti-Saccharomyces cerevisiae antibody Anti-Saccharomyces cerevisiae Antibody (ASCA) was initially discovered to target the cell wall of Saccharomyces cerevisiae, but it is now observed in some instances of IBD.</abstract><cop>Nashville</cop><pub>Endeavor Business Media</pub><tpages>6</tpages></addata></record> |
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subjects | Analysis Antibodies Antigens Bacteria Biological markers Biomarkers Crohn's disease Cytokines Diagnosis Endoscopy Feces Health aspects Immune system Inflammation Inflammatory bowel disease Inflammatory bowel diseases Inflammatory diseases Irritable bowel syndrome Metabolites Microbiota Patients Permeability Remission (Medicine) Yeast |
title | The prospective use of cytokine markers for inflammatory bowel disease evaluation |
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