{"id":11019,"date":"2024-06-26T16:04:00","date_gmt":"2024-06-26T14:04:00","guid":{"rendered":"https:\/\/www.adacyte.com\/?post_type=scientific-corner&#038;p=11019"},"modified":"2025-08-07T16:09:48","modified_gmt":"2025-08-07T14:09:48","slug":"fecal-and-serum-granulocyte-protein-levels-in-inflammatory-bowel-disease-and-irritable-bowel-syndrome-and-their-relation-to-disease-activity","status":"publish","type":"scientific-corner","link":"https:\/\/www.adacyte.com\/de\/professional\/scientific-corner\/fecal-and-serum-granulocyte-protein-levels-in-inflammatory-bowel-disease-and-irritable-bowel-syndrome-and-their-relation-to-disease-activity\/","title":{"rendered":"Fecal and Serum Granulocyte Protein Levels in Inflammatory Bowel Disease and Irritable Bowel Syndrome and Their Relation to Disease Activity"},"content":{"rendered":"<div class=\"post-content max-w-987 mx-auto px-20 lg:px-0\">\n<p><a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Ekoff%20H%22%5BAuthor%5D\">Helena Ekoff<\/a>\u00a0<sup>1,2<\/sup>,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Rydell%20N%22%5BAuthor%5D\">Niclas Rydell<\/a>\u00a0<sup>1,\u2709<\/sup>,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Hellstr%C3%B6m%20PM%22%5BAuthor%5D\">Per M Hellstr\u00f6m<\/a>\u00a0<sup>2<\/sup>,\u00a0<a href=\"https:\/\/pubmed.ncbi.nlm.nih.gov\/?term=%22Mov%C3%A9rare%20R%22%5BAuthor%5D\">Robert Mov\u00e9rare<\/a>\u00a0<sup>1,3<\/sup><\/p>\n<\/div>\n\n<div class=\"post-content max-w-987 mx-auto px-20 lg:px-0\">\n<p>Clin Transl Gastroenterol. 2024 Jun 26;15(10):e1.doi:\u00a0<a href=\"https:\/\/doi.org\/10.14309\/ctg.0000000000000733\" target=\"_blank\" rel=\"noreferrer noopener\">10.14309\/ctg.0000000000000733<\/a><\/p>\n<\/div>\n\n<div class=\"post-content max-w-987 mx-auto px-20 lg:px-0\">\n<h3 class=\"wp-block-heading\">INTRODUCTION:<\/h3>\n<\/div>\n\n<div class=\"post-content max-w-987 mx-auto px-20 lg:px-0\">\n<p>Neutrophilic calprotectin (CP) and myeloperoxidase (MPO), neutrophil gelatinase-associated lipocalin (NGAL), and eosinophil-derived neurotoxin (EDN) are suggested proxy markers for gut inflammation. However, there are insufficient supporting data for MPO, NGAL, and EDN.<\/p>\n<\/div>\n\n<div class=\"post-content max-w-987 mx-auto px-20 lg:px-0\">\n<h3 class=\"wp-block-heading\">METHODS:<\/h3>\n<\/div>\n\n<div class=\"post-content max-w-987 mx-auto px-20 lg:px-0\">\n<p>In a cross-sectional investigation including adult patients, we studied the ability of CP, MPO, NGAL, and EDN, measured in fecal and serum samples, to differentiate between inflammatory bowel disease (IBD) and irritable bowel syndrome (IBS), and to predict disease activity.<\/p>\n<\/div>\n\n<div class=\"post-content max-w-987 mx-auto px-20 lg:px-0\">\n<h3 class=\"wp-block-heading\">RESULTS:<\/h3>\n<\/div>\n\n<div class=\"post-content max-w-987 mx-auto px-20 lg:px-0\">\n<p>Fifty-nine patients had ulcerative colitis (UC), 38 had Crohn&#8217;s disease, and 100 patients had IBS. The protein concentrations were higher in patients with IBD in the fecal samples (<em>P<\/em>&nbsp;&lt; 0.001) and the serum samples (<em>P<\/em>&nbsp;&lt; 0.01), and they correlated weakly (r<sub>s<\/sub>&nbsp;\u22640.38) between the sample sources. Fecal EDN was higher in patients with Crohn&#8217;s disease compared with UC (1.79 vs 0.50 mg\/kg,&nbsp;<em>P<\/em>&nbsp;= 0.016). The neutrophilic proteins were superior to EDN in the fecal samples for differentiating between patients with IBD and IBS. Fecal MPO (cutoff: 0.86 mg\/kg) had the highest sensitivity (74.7%) and specificity (84.6%). Combining fecal CP and MPO increased the sensitivity to 82.3% (specificity: 73.6%). NGAL (cutoff: 196.9 \u03bcg\/L) showed the best discriminating performance in serum (sensitivity: 62.9%; specificity: 68.0%). Serum NGAL (cutoff: 272.4 \u03bcg\/L) predicted active disease in UC (Partial Mayo Score \u22652) with a sensitivity and specificity of 57.1% and 83.3%, respectively.<\/p>\n<\/div>\n\n<div class=\"post-content max-w-987 mx-auto px-20 lg:px-0\">\n<h3 class=\"wp-block-heading\">DISCUSSION: <strong>Fecal MPO and serum NGAL are promising novel biomarkers, in addition to fecal CP, for differentiating between IBD and IBS. Serum NGAL may also predict disease activity in patients with UC.<\/strong><\/h3>\n<\/div>","protected":false},"excerpt":{"rendered":"<p>Helena Ekoff\u00a01,2,\u00a0Niclas Rydell\u00a01,\u2709,\u00a0Per M Hellstr\u00f6m\u00a02,\u00a0Robert Mov\u00e9rare\u00a01,3 Clin Transl Gastroenterol. 2024 Jun 26;15(10):e1.doi:\u00a010.14309\/ctg.0000000000000733 INTRODUCTION: Neutrophilic calprotectin (CP) and myeloperoxidase (MPO), neutrophil gelatinase-associated lipocalin (NGAL), and eosinophil-derived neurotoxin (EDN) are suggested proxy markers for gut inflammation. However, there are insufficient supporting data for MPO, NGAL, and EDN. METHODS: In a cross-sectional investigation including adult patients, we studied [&hellip;]<\/p>\n","protected":false},"template":"","scientific_tags":[483,347,855,858,859,860,654,105,426,856,581,445,857,155],"class_list":["post-11019","scientific-corner","type-scientific-corner","status-publish","hentry","scientific_tags-biomarkers","scientific_tags-diagnostic-criteria","scientific_tags-disease-activity","scientific_tags-edn","scientific_tags-eosinophil","scientific_tags-fecal","scientific_tags-fecal-calprotectin","scientific_tags-granulocyte","scientific_tags-ibd","scientific_tags-ibs","scientific_tags-mpo","scientific_tags-neutrophil","scientific_tags-ngal","scientific_tags-serum"],"acf":{"sc_authors":"<a href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC11500791\/\">Fecal and Serum Granulocyte Protein Levels in Inflammatory Bowel Disease and Irritable Bowel Syndrome and Their Relation to Disease Activity - PMC<\/a>\r\n\r\n<a href=\"https:\/\/pmc.ncbi.nlm.nih.gov\/articles\/PMC11500791\/pdf\/ct9-15-e1f.pdf\">CTG-24-0044 1..10<\/a>"},"yoast_head":"<!-- This site is optimized with the Yoast SEO plugin v22.9 - https:\/\/yoast.com\/wordpress\/plugins\/seo\/ -->\n<title>Fecal and Serum Granulocyte Protein Levels in Inflammatory Bowel Disease and Irritable Bowel Syndrome and Their Relation to Disease Activity - Adacyte<\/title>\n<meta name=\"robots\" content=\"index, follow, max-snippet:-1, max-image-preview:large, max-video-preview:-1\" \/>\n<link rel=\"canonical\" href=\"https:\/\/www.adacyte.com\/de\/professional\/scientific-corner\/fecal-and-serum-granulocyte-protein-levels-in-inflammatory-bowel-disease-and-irritable-bowel-syndrome-and-their-relation-to-disease-activity\/\" \/>\n<meta property=\"og:locale\" content=\"de_DE\" \/>\n<meta property=\"og:type\" content=\"article\" \/>\n<meta property=\"og:title\" content=\"Fecal and Serum Granulocyte Protein Levels in Inflammatory Bowel Disease and Irritable Bowel Syndrome and Their Relation to Disease Activity - Adacyte\" \/>\n<meta property=\"og:description\" content=\"Helena Ekoff\u00a01,2,\u00a0Niclas Rydell\u00a01,\u2709,\u00a0Per M Hellstr\u00f6m\u00a02,\u00a0Robert Mov\u00e9rare\u00a01,3 Clin Transl Gastroenterol. 2024 Jun 26;15(10):e1.doi:\u00a010.14309\/ctg.0000000000000733 INTRODUCTION: Neutrophilic calprotectin (CP) and myeloperoxidase (MPO), neutrophil gelatinase-associated lipocalin (NGAL), and eosinophil-derived neurotoxin (EDN) are suggested proxy markers for gut inflammation. However, there are insufficient supporting data for MPO, NGAL, and EDN. 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