Loading…

Diagnostic Potential of Systemic Eosinophil-Associated Cytokines and Growth Factors in IBD

Despite the acknowledged contribution of eosinophils to the disease pathogenesis, available data on cytokines closely related to the peripheral eosinophils in inflammatory bowel disease (IBD) are scattered. We assessed the concentrations of eosinophil-associated cytokines and growth factors in the g...

Full description

Saved in:
Bibliographic Details
Published in:Gastroenterology research and practice 2018-01, Vol.2018 (2018), p.1-10
Main Authors: Gamian, Andrzej, Gorska, Sabina, Bednarz-Misa, Iwona, Matusiewicz, Malgorzata, Neubauer, Katarzyna, Krzystek-Korpacka, Malgorzata
Format: Article
Language:English
Subjects:
Citations: Items that this one cites
Items that cite this one
Online Access:Get full text
Tags: Add Tag
No Tags, Be the first to tag this record!
cited_by cdi_FETCH-LOGICAL-c604t-e552c4019dbba280395e53686510e8f0b736b65b31bb34273e1adc3d4d7450e43
cites cdi_FETCH-LOGICAL-c604t-e552c4019dbba280395e53686510e8f0b736b65b31bb34273e1adc3d4d7450e43
container_end_page 10
container_issue 2018
container_start_page 1
container_title Gastroenterology research and practice
container_volume 2018
creator Gamian, Andrzej
Gorska, Sabina
Bednarz-Misa, Iwona
Matusiewicz, Malgorzata
Neubauer, Katarzyna
Krzystek-Korpacka, Malgorzata
description Despite the acknowledged contribution of eosinophils to the disease pathogenesis, available data on cytokines closely related to the peripheral eosinophils in inflammatory bowel disease (IBD) are scattered. We assessed the concentrations of eosinophil-associated cytokines and growth factors in the group of 277 individuals (101 patients with Crohn’s disease (CD), 77 with ulcerative colitis (UC), 16 with irritable bowel syndrome (IBS), and 83 healthy controls) and referred to IBD activity and the levels of hsCRP. As compared to IBS patients or healthy controls, patients with CD had significantly higher levels of IL5, IL8, IL12(p70), GM-CSF, and TNFα and patients with UC, the levels of eotaxin, IL4, IL5, IL8, IL12(p70), IL13, GM-CSF, and TNFα were also higher. As compared to CD patients, patients with UC had significantly higher levels of eotaxin, IL4, IL5, IL8, and IL1. In turn, the concentrations of hsCRP were significantly higher in CD than UC. Except for IL13, all cytokines and hsCRP positively correlated with CDAI. In UC, a positive correlation with MDAI was observed for hsCRP, GM-CSF, IL12(p70), and IFNγ and a negative one for IL8. The concentrations of hsCRP, GM-CSF, IFNγ, IL12(p70), and RANTES were higher in UC patients with active than inactive disease whereas those of IL8 and TNFα were significantly lower. Eotaxin, determined individually or in a panel with IFNγ and hsCRP, showed fair accuracy in differentiating CD from UC. If confirmed on a larger representation of IBS patients, IL8 might support differential diagnosis of organic and functional conditions of the bowel. GM-CSF, in turn, demonstrated to be an excellent indicator of bowel inflammation and may be taken into consideration as a noninvasive marker of mucosal healing. In summary, eosinophil-associated cytokines are elevated in IBD, more pronouncedly in UC, and may support the differential diagnosis of IBD and aid in monitoring of mucosal healing.
doi_str_mv 10.1155/2018/7265812
format article
fullrecord <record><control><sourceid>gale_doaj_</sourceid><recordid>TN_cdi_doaj_primary_oai_doaj_org_article_cabd33954e594521a7cfb36124a8b2ed</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><galeid>A575112444</galeid><doaj_id>oai_doaj_org_article_cabd33954e594521a7cfb36124a8b2ed</doaj_id><sourcerecordid>A575112444</sourcerecordid><originalsourceid>FETCH-LOGICAL-c604t-e552c4019dbba280395e53686510e8f0b736b65b31bb34273e1adc3d4d7450e43</originalsourceid><addsrcrecordid>eNqNktuLEzEUhwdR3HX1zWcZ8EXQ7uae6YtQuxcLCwoqiC8hlzNt6jSpydSl_70Z29214oMMzIQzX77M-c2pqucYnWLM-RlBuDmTRPAGkwfVMRaNHAmKvj68XWOCj6onOS8REgQh_rg6oggzKfH4uPp27vU8xNx7W3-MPYTe666Obf1pm3tYlepFzD7E9cJ3o0nO0Xrdg6un2z5-9wFyrYOrr1K86Rf1pbZ9TLn2oZ69O39aPWp1l-HZ_nlSfbm8-Dx9P7r-cDWbTq5HViDWj4BzYhnCY2eMJg2iYw6cikZwjKBpkZFUGMENxcZQRiQFrJ2ljjnJOAJGT6rZzuuiXqp18iudtipqr34XYpornUp_HSirjaPlAAZ8zDjBWtrW0JIQ040h4Irr7c613pgVOFvySLo7kB6-CX6h5vGnEqihgtEieLUXpPhjA7lXK58tdJ0OEDdZETRmrNy4LOjLv9Bl3KRQoipUsWHcsOaemuvSgA9tLOfaQaomXHJcvp0NGZz-gyqXG_5hDND6Uj_Y8Ga3waaYc4L2rkeM1DBXapgrtZ-rgr_4M5c7-HaQCvB6Byx8cPrG_6cOCgOtvqex4EwK-gtkxtxs</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2083611848</pqid></control><display><type>article</type><title>Diagnostic Potential of Systemic Eosinophil-Associated Cytokines and Growth Factors in IBD</title><source>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</source><source>Wiley Open Access</source><source>PubMed Central</source><creator>Gamian, Andrzej ; Gorska, Sabina ; Bednarz-Misa, Iwona ; Matusiewicz, Malgorzata ; Neubauer, Katarzyna ; Krzystek-Korpacka, Malgorzata</creator><contributor>M'Koma, Amosy ; Amosy M'Koma</contributor><creatorcontrib>Gamian, Andrzej ; Gorska, Sabina ; Bednarz-Misa, Iwona ; Matusiewicz, Malgorzata ; Neubauer, Katarzyna ; Krzystek-Korpacka, Malgorzata ; M'Koma, Amosy ; Amosy M'Koma</creatorcontrib><description>Despite the acknowledged contribution of eosinophils to the disease pathogenesis, available data on cytokines closely related to the peripheral eosinophils in inflammatory bowel disease (IBD) are scattered. We assessed the concentrations of eosinophil-associated cytokines and growth factors in the group of 277 individuals (101 patients with Crohn’s disease (CD), 77 with ulcerative colitis (UC), 16 with irritable bowel syndrome (IBS), and 83 healthy controls) and referred to IBD activity and the levels of hsCRP. As compared to IBS patients or healthy controls, patients with CD had significantly higher levels of IL5, IL8, IL12(p70), GM-CSF, and TNFα and patients with UC, the levels of eotaxin, IL4, IL5, IL8, IL12(p70), IL13, GM-CSF, and TNFα were also higher. As compared to CD patients, patients with UC had significantly higher levels of eotaxin, IL4, IL5, IL8, and IL1. In turn, the concentrations of hsCRP were significantly higher in CD than UC. Except for IL13, all cytokines and hsCRP positively correlated with CDAI. In UC, a positive correlation with MDAI was observed for hsCRP, GM-CSF, IL12(p70), and IFNγ and a negative one for IL8. The concentrations of hsCRP, GM-CSF, IFNγ, IL12(p70), and RANTES were higher in UC patients with active than inactive disease whereas those of IL8 and TNFα were significantly lower. Eotaxin, determined individually or in a panel with IFNγ and hsCRP, showed fair accuracy in differentiating CD from UC. If confirmed on a larger representation of IBS patients, IL8 might support differential diagnosis of organic and functional conditions of the bowel. GM-CSF, in turn, demonstrated to be an excellent indicator of bowel inflammation and may be taken into consideration as a noninvasive marker of mucosal healing. In summary, eosinophil-associated cytokines are elevated in IBD, more pronouncedly in UC, and may support the differential diagnosis of IBD and aid in monitoring of mucosal healing.</description><identifier>ISSN: 1687-6121</identifier><identifier>EISSN: 1687-630X</identifier><identifier>DOI: 10.1155/2018/7265812</identifier><identifier>PMID: 30147719</identifier><language>eng</language><publisher>Cairo, Egypt: Hindawi Publishing Corporation</publisher><subject>Biomarkers ; Blood &amp; organ donations ; Chemokines ; Colon ; Comparative analysis ; Cytokines ; Endoscopy ; Family medical history ; Gastroenterology ; Granulocytes ; Growth factors ; Hepatology ; Inflammation ; Inflammatory bowel disease ; Irritable bowel syndrome ; Kinases ; Pathogenesis ; Pediatrics ; Proteins ; Tumor necrosis factor ; Ulcerative colitis</subject><ispartof>Gastroenterology research and practice, 2018-01, Vol.2018 (2018), p.1-10</ispartof><rights>Copyright © 2018 Katarzyna Neubauer et al.</rights><rights>COPYRIGHT 2018 John Wiley &amp; Sons, Inc.</rights><rights>Copyright © 2018 Katarzyna Neubauer et al. This is an open access article distributed under the Creative Commons Attribution License (the “License”), which permits unrestricted use, distribution, and reproduction in any medium, provided the original work is properly cited. Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License. http://creativecommons.org/licenses/by/4.0</rights><rights>Copyright © 2018 Katarzyna Neubauer et al. 2018</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c604t-e552c4019dbba280395e53686510e8f0b736b65b31bb34273e1adc3d4d7450e43</citedby><cites>FETCH-LOGICAL-c604t-e552c4019dbba280395e53686510e8f0b736b65b31bb34273e1adc3d4d7450e43</cites><orcidid>0000-0003-4624-0109 ; 0000-0003-3650-9311 ; 0000-0001-7244-2017 ; 0000-0002-2753-8092</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/2083611848/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2083611848?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,727,780,784,885,25753,27924,27925,37012,37013,44590,53791,53793,74998</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/30147719$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><contributor>M'Koma, Amosy</contributor><contributor>Amosy M'Koma</contributor><creatorcontrib>Gamian, Andrzej</creatorcontrib><creatorcontrib>Gorska, Sabina</creatorcontrib><creatorcontrib>Bednarz-Misa, Iwona</creatorcontrib><creatorcontrib>Matusiewicz, Malgorzata</creatorcontrib><creatorcontrib>Neubauer, Katarzyna</creatorcontrib><creatorcontrib>Krzystek-Korpacka, Malgorzata</creatorcontrib><title>Diagnostic Potential of Systemic Eosinophil-Associated Cytokines and Growth Factors in IBD</title><title>Gastroenterology research and practice</title><addtitle>Gastroenterol Res Pract</addtitle><description>Despite the acknowledged contribution of eosinophils to the disease pathogenesis, available data on cytokines closely related to the peripheral eosinophils in inflammatory bowel disease (IBD) are scattered. We assessed the concentrations of eosinophil-associated cytokines and growth factors in the group of 277 individuals (101 patients with Crohn’s disease (CD), 77 with ulcerative colitis (UC), 16 with irritable bowel syndrome (IBS), and 83 healthy controls) and referred to IBD activity and the levels of hsCRP. As compared to IBS patients or healthy controls, patients with CD had significantly higher levels of IL5, IL8, IL12(p70), GM-CSF, and TNFα and patients with UC, the levels of eotaxin, IL4, IL5, IL8, IL12(p70), IL13, GM-CSF, and TNFα were also higher. As compared to CD patients, patients with UC had significantly higher levels of eotaxin, IL4, IL5, IL8, and IL1. In turn, the concentrations of hsCRP were significantly higher in CD than UC. Except for IL13, all cytokines and hsCRP positively correlated with CDAI. In UC, a positive correlation with MDAI was observed for hsCRP, GM-CSF, IL12(p70), and IFNγ and a negative one for IL8. The concentrations of hsCRP, GM-CSF, IFNγ, IL12(p70), and RANTES were higher in UC patients with active than inactive disease whereas those of IL8 and TNFα were significantly lower. Eotaxin, determined individually or in a panel with IFNγ and hsCRP, showed fair accuracy in differentiating CD from UC. If confirmed on a larger representation of IBS patients, IL8 might support differential diagnosis of organic and functional conditions of the bowel. GM-CSF, in turn, demonstrated to be an excellent indicator of bowel inflammation and may be taken into consideration as a noninvasive marker of mucosal healing. In summary, eosinophil-associated cytokines are elevated in IBD, more pronouncedly in UC, and may support the differential diagnosis of IBD and aid in monitoring of mucosal healing.</description><subject>Biomarkers</subject><subject>Blood &amp; organ donations</subject><subject>Chemokines</subject><subject>Colon</subject><subject>Comparative analysis</subject><subject>Cytokines</subject><subject>Endoscopy</subject><subject>Family medical history</subject><subject>Gastroenterology</subject><subject>Granulocytes</subject><subject>Growth factors</subject><subject>Hepatology</subject><subject>Inflammation</subject><subject>Inflammatory bowel disease</subject><subject>Irritable bowel syndrome</subject><subject>Kinases</subject><subject>Pathogenesis</subject><subject>Pediatrics</subject><subject>Proteins</subject><subject>Tumor necrosis factor</subject><subject>Ulcerative colitis</subject><issn>1687-6121</issn><issn>1687-630X</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2018</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNqNktuLEzEUhwdR3HX1zWcZ8EXQ7uae6YtQuxcLCwoqiC8hlzNt6jSpydSl_70Z29214oMMzIQzX77M-c2pqucYnWLM-RlBuDmTRPAGkwfVMRaNHAmKvj68XWOCj6onOS8REgQh_rg6oggzKfH4uPp27vU8xNx7W3-MPYTe666Obf1pm3tYlepFzD7E9cJ3o0nO0Xrdg6un2z5-9wFyrYOrr1K86Rf1pbZ9TLn2oZ69O39aPWp1l-HZ_nlSfbm8-Dx9P7r-cDWbTq5HViDWj4BzYhnCY2eMJg2iYw6cikZwjKBpkZFUGMENxcZQRiQFrJ2ljjnJOAJGT6rZzuuiXqp18iudtipqr34XYpornUp_HSirjaPlAAZ8zDjBWtrW0JIQ040h4Irr7c613pgVOFvySLo7kB6-CX6h5vGnEqihgtEieLUXpPhjA7lXK58tdJ0OEDdZETRmrNy4LOjLv9Bl3KRQoipUsWHcsOaemuvSgA9tLOfaQaomXHJcvp0NGZz-gyqXG_5hDND6Uj_Y8Ga3waaYc4L2rkeM1DBXapgrtZ-rgr_4M5c7-HaQCvB6Byx8cPrG_6cOCgOtvqex4EwK-gtkxtxs</recordid><startdate>20180101</startdate><enddate>20180101</enddate><creator>Gamian, Andrzej</creator><creator>Gorska, Sabina</creator><creator>Bednarz-Misa, Iwona</creator><creator>Matusiewicz, Malgorzata</creator><creator>Neubauer, Katarzyna</creator><creator>Krzystek-Korpacka, Malgorzata</creator><general>Hindawi Publishing Corporation</general><general>Hindawi</general><general>John Wiley &amp; Sons, Inc</general><general>Hindawi Limited</general><scope>ADJCN</scope><scope>AHFXO</scope><scope>RHU</scope><scope>RHW</scope><scope>RHX</scope><scope>NPM</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7XB</scope><scope>8FK</scope><scope>8G5</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>GNUQQ</scope><scope>GUQSH</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope><orcidid>https://orcid.org/0000-0003-4624-0109</orcidid><orcidid>https://orcid.org/0000-0003-3650-9311</orcidid><orcidid>https://orcid.org/0000-0001-7244-2017</orcidid><orcidid>https://orcid.org/0000-0002-2753-8092</orcidid></search><sort><creationdate>20180101</creationdate><title>Diagnostic Potential of Systemic Eosinophil-Associated Cytokines and Growth Factors in IBD</title><author>Gamian, Andrzej ; Gorska, Sabina ; Bednarz-Misa, Iwona ; Matusiewicz, Malgorzata ; Neubauer, Katarzyna ; Krzystek-Korpacka, Malgorzata</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c604t-e552c4019dbba280395e53686510e8f0b736b65b31bb34273e1adc3d4d7450e43</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2018</creationdate><topic>Biomarkers</topic><topic>Blood &amp; organ donations</topic><topic>Chemokines</topic><topic>Colon</topic><topic>Comparative analysis</topic><topic>Cytokines</topic><topic>Endoscopy</topic><topic>Family medical history</topic><topic>Gastroenterology</topic><topic>Granulocytes</topic><topic>Growth factors</topic><topic>Hepatology</topic><topic>Inflammation</topic><topic>Inflammatory bowel disease</topic><topic>Irritable bowel syndrome</topic><topic>Kinases</topic><topic>Pathogenesis</topic><topic>Pediatrics</topic><topic>Proteins</topic><topic>Tumor necrosis factor</topic><topic>Ulcerative colitis</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Gamian, Andrzej</creatorcontrib><creatorcontrib>Gorska, Sabina</creatorcontrib><creatorcontrib>Bednarz-Misa, Iwona</creatorcontrib><creatorcontrib>Matusiewicz, Malgorzata</creatorcontrib><creatorcontrib>Neubauer, Katarzyna</creatorcontrib><creatorcontrib>Krzystek-Korpacka, Malgorzata</creatorcontrib><collection>الدوريات العلمية والإحصائية - e-Marefa Academic and Statistical Periodicals</collection><collection>معرفة - المحتوى العربي الأكاديمي المتكامل - e-Marefa Academic Complete</collection><collection>Hindawi Publishing Complete</collection><collection>Hindawi Publishing Subscription Journals</collection><collection>Hindawi Publishing Open Access Journals</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>ProQuest Central (purchase pre-March 2016)</collection><collection>ProQuest Central (Alumni) (purchase pre-March 2016)</collection><collection>Research Library (Alumni Edition)</collection><collection>ProQuest Central (Alumni)</collection><collection>ProQuest Central</collection><collection>ProQuest Central Essentials</collection><collection>ProQuest Central</collection><collection>ProQuest One Community College</collection><collection>ProQuest Central</collection><collection>ProQuest Central Student</collection><collection>Research Library Prep</collection><collection>ProQuest Research Library</collection><collection>Research Library (Corporate)</collection><collection>Publicly Available Content Database (Proquest) (PQ_SDU_P3)</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 Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Gastroenterology research and practice</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Gamian, Andrzej</au><au>Gorska, Sabina</au><au>Bednarz-Misa, Iwona</au><au>Matusiewicz, Malgorzata</au><au>Neubauer, Katarzyna</au><au>Krzystek-Korpacka, Malgorzata</au><au>M'Koma, Amosy</au><au>Amosy M'Koma</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Diagnostic Potential of Systemic Eosinophil-Associated Cytokines and Growth Factors in IBD</atitle><jtitle>Gastroenterology research and practice</jtitle><addtitle>Gastroenterol Res Pract</addtitle><date>2018-01-01</date><risdate>2018</risdate><volume>2018</volume><issue>2018</issue><spage>1</spage><epage>10</epage><pages>1-10</pages><issn>1687-6121</issn><eissn>1687-630X</eissn><abstract>Despite the acknowledged contribution of eosinophils to the disease pathogenesis, available data on cytokines closely related to the peripheral eosinophils in inflammatory bowel disease (IBD) are scattered. We assessed the concentrations of eosinophil-associated cytokines and growth factors in the group of 277 individuals (101 patients with Crohn’s disease (CD), 77 with ulcerative colitis (UC), 16 with irritable bowel syndrome (IBS), and 83 healthy controls) and referred to IBD activity and the levels of hsCRP. As compared to IBS patients or healthy controls, patients with CD had significantly higher levels of IL5, IL8, IL12(p70), GM-CSF, and TNFα and patients with UC, the levels of eotaxin, IL4, IL5, IL8, IL12(p70), IL13, GM-CSF, and TNFα were also higher. As compared to CD patients, patients with UC had significantly higher levels of eotaxin, IL4, IL5, IL8, and IL1. In turn, the concentrations of hsCRP were significantly higher in CD than UC. Except for IL13, all cytokines and hsCRP positively correlated with CDAI. In UC, a positive correlation with MDAI was observed for hsCRP, GM-CSF, IL12(p70), and IFNγ and a negative one for IL8. The concentrations of hsCRP, GM-CSF, IFNγ, IL12(p70), and RANTES were higher in UC patients with active than inactive disease whereas those of IL8 and TNFα were significantly lower. Eotaxin, determined individually or in a panel with IFNγ and hsCRP, showed fair accuracy in differentiating CD from UC. If confirmed on a larger representation of IBS patients, IL8 might support differential diagnosis of organic and functional conditions of the bowel. GM-CSF, in turn, demonstrated to be an excellent indicator of bowel inflammation and may be taken into consideration as a noninvasive marker of mucosal healing. In summary, eosinophil-associated cytokines are elevated in IBD, more pronouncedly in UC, and may support the differential diagnosis of IBD and aid in monitoring of mucosal healing.</abstract><cop>Cairo, Egypt</cop><pub>Hindawi Publishing Corporation</pub><pmid>30147719</pmid><doi>10.1155/2018/7265812</doi><tpages>10</tpages><orcidid>https://orcid.org/0000-0003-4624-0109</orcidid><orcidid>https://orcid.org/0000-0003-3650-9311</orcidid><orcidid>https://orcid.org/0000-0001-7244-2017</orcidid><orcidid>https://orcid.org/0000-0002-2753-8092</orcidid><oa>free_for_read</oa></addata></record>
fulltext fulltext
identifier ISSN: 1687-6121
ispartof Gastroenterology research and practice, 2018-01, Vol.2018 (2018), p.1-10
issn 1687-6121
1687-630X
language eng
recordid cdi_doaj_primary_oai_doaj_org_article_cabd33954e594521a7cfb36124a8b2ed
source Publicly Available Content Database (Proquest) (PQ_SDU_P3); Wiley Open Access; PubMed Central
subjects Biomarkers
Blood & organ donations
Chemokines
Colon
Comparative analysis
Cytokines
Endoscopy
Family medical history
Gastroenterology
Granulocytes
Growth factors
Hepatology
Inflammation
Inflammatory bowel disease
Irritable bowel syndrome
Kinases
Pathogenesis
Pediatrics
Proteins
Tumor necrosis factor
Ulcerative colitis
title Diagnostic Potential of Systemic Eosinophil-Associated Cytokines and Growth Factors in IBD
url http://sfxeu10.hosted.exlibrisgroup.com/loughborough?ctx_ver=Z39.88-2004&ctx_enc=info:ofi/enc:UTF-8&ctx_tim=2025-01-07T15%3A25%3A03IST&url_ver=Z39.88-2004&url_ctx_fmt=infofi/fmt:kev:mtx:ctx&rfr_id=info:sid/primo.exlibrisgroup.com:primo3-Article-gale_doaj_&rft_val_fmt=info:ofi/fmt:kev:mtx:journal&rft.genre=article&rft.atitle=Diagnostic%20Potential%20of%20Systemic%20Eosinophil-Associated%20Cytokines%20and%20Growth%20Factors%20in%20IBD&rft.jtitle=Gastroenterology%20research%20and%20practice&rft.au=Gamian,%20Andrzej&rft.date=2018-01-01&rft.volume=2018&rft.issue=2018&rft.spage=1&rft.epage=10&rft.pages=1-10&rft.issn=1687-6121&rft.eissn=1687-630X&rft_id=info:doi/10.1155/2018/7265812&rft_dat=%3Cgale_doaj_%3EA575112444%3C/gale_doaj_%3E%3Cgrp_id%3Ecdi_FETCH-LOGICAL-c604t-e552c4019dbba280395e53686510e8f0b736b65b31bb34273e1adc3d4d7450e43%3C/grp_id%3E%3Coa%3E%3C/oa%3E%3Curl%3E%3C/url%3E&rft_id=info:oai/&rft_pqid=2083611848&rft_id=info:pmid/30147719&rft_galeid=A575112444&rfr_iscdi=true