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Interleukin-17 as a biomarker for lupus nephritis: correlation with disease activity indices and histopathological classification
Background Lupus nephritis (LN) is one of the devastating manifestations of systemic lupus erythematosus (SLE). It is a leading cause of death in SLE patients. Interleukin 17(IL-17) is involved in the development of several autoimmune diseases. It causes inflammation and organ damage by exaggerating...
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Published in: | Egyptian Rheumatology and Rehabilitation 2024-07, Vol.51 (1), p.36-7, Article 36 |
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description | Background
Lupus nephritis (LN) is one of the devastating manifestations of systemic lupus erythematosus (SLE). It is a leading cause of death in SLE patients. Interleukin 17(IL-17) is involved in the development of several autoimmune diseases. It causes inflammation and organ damage by exaggerating the immune response and augmenting antibody production by B cells. We assessed the role of IL-17A in LN and its relation to other markers of disease activity and different histopathological classes.
Results
We evaluated serum IL-17A in forty LN patients and thirty SLE patients without LN (non-LN). We found that LN patients had a significantly higher IL-17A level in comparison to non-LN. In the LN group, IL-17A was positively correlated with the systemic lupus erythematosus disease activity index (SLEDAI), protein/creatinine (P/C) ratio, 24-hour urinary proteins, anti-nucleosome, and anti-dsDNA antibodies and negatively correlated with C3 and C4. IL-17A was higher in class III and IV compared to class II and V LN. ROC curve analysis of IL-17A revealed 75% sensitivity and 76.7% specificity for LN, and the AUC was 0.791.
Conclusion
Lupus nephritis patients have a higher serum level of IL-17A than those without LN, which is more pronounced in patients with class-III and IV LN. Moreover, IL-17A has good sensitivity and specificity for LN and correlates with the disease activity indices; hence, it may be a prognostic marker for LN in SLE patients. |
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Lupus nephritis (LN) is one of the devastating manifestations of systemic lupus erythematosus (SLE). It is a leading cause of death in SLE patients. Interleukin 17(IL-17) is involved in the development of several autoimmune diseases. It causes inflammation and organ damage by exaggerating the immune response and augmenting antibody production by B cells. We assessed the role of IL-17A in LN and its relation to other markers of disease activity and different histopathological classes.
Results
We evaluated serum IL-17A in forty LN patients and thirty SLE patients without LN (non-LN). We found that LN patients had a significantly higher IL-17A level in comparison to non-LN. In the LN group, IL-17A was positively correlated with the systemic lupus erythematosus disease activity index (SLEDAI), protein/creatinine (P/C) ratio, 24-hour urinary proteins, anti-nucleosome, and anti-dsDNA antibodies and negatively correlated with C3 and C4. IL-17A was higher in class III and IV compared to class II and V LN. ROC curve analysis of IL-17A revealed 75% sensitivity and 76.7% specificity for LN, and the AUC was 0.791.
Conclusion
Lupus nephritis patients have a higher serum level of IL-17A than those without LN, which is more pronounced in patients with class-III and IV LN. Moreover, IL-17A has good sensitivity and specificity for LN and correlates with the disease activity indices; hence, it may be a prognostic marker for LN in SLE patients.</description><identifier>ISSN: 2090-3235</identifier><identifier>ISSN: 1110-161X</identifier><identifier>EISSN: 2090-3235</identifier><identifier>DOI: 10.1186/s43166-024-00268-3</identifier><language>eng</language><publisher>Berlin/Heidelberg: Springer Berlin Heidelberg</publisher><subject>Arthritis ; Autoimmune diseases ; Biopsy ; Chi-square test ; Creatinine ; Cytokines ; Disease ; Hypertension ; IL-17A ; Laboratories ; Lupus ; Medicine ; Medicine & Public Health ; Pathogenesis ; Proteins ; Rehabilitation ; SLE ; Ulcers</subject><ispartof>Egyptian Rheumatology and Rehabilitation, 2024-07, Vol.51 (1), p.36-7, Article 36</ispartof><rights>The Author(s) 2024</rights><rights>The Author(s) 2024. This work is published under http://creativecommons.org/licenses/by/4.0/ (the “License”). Notwithstanding the ProQuest Terms and Conditions, you may use this content in accordance with the terms of the License.</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><cites>FETCH-LOGICAL-c310t-30a5cc2b02dce668881a33aea735c0bbc236777ec8a4b1fbbf001c576609e2503</cites><orcidid>0009-0007-8414-7040 ; 0000-0001-8755-1750 ; 0000-0002-7315-4524 ; 0009-0003-7688-0358</orcidid></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.proquest.com/docview/3075499314/fulltextPDF?pq-origsite=primo$$EPDF$$P50$$Gproquest$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/3075499314?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>314,776,780,25733,27903,27904,36991,44569,74872</link.rule.ids></links><search><creatorcontrib>Ahmed, Aya M.</creatorcontrib><creatorcontrib>Ahmed, Abdullatif A.</creatorcontrib><creatorcontrib>Ismail, Faten</creatorcontrib><creatorcontrib>Elsayed, Sahar A.</creatorcontrib><title>Interleukin-17 as a biomarker for lupus nephritis: correlation with disease activity indices and histopathological classification</title><title>Egyptian Rheumatology and Rehabilitation</title><addtitle>Egypt Rheumatol Rehabil</addtitle><description>Background
Lupus nephritis (LN) is one of the devastating manifestations of systemic lupus erythematosus (SLE). It is a leading cause of death in SLE patients. Interleukin 17(IL-17) is involved in the development of several autoimmune diseases. It causes inflammation and organ damage by exaggerating the immune response and augmenting antibody production by B cells. We assessed the role of IL-17A in LN and its relation to other markers of disease activity and different histopathological classes.
Results
We evaluated serum IL-17A in forty LN patients and thirty SLE patients without LN (non-LN). We found that LN patients had a significantly higher IL-17A level in comparison to non-LN. In the LN group, IL-17A was positively correlated with the systemic lupus erythematosus disease activity index (SLEDAI), protein/creatinine (P/C) ratio, 24-hour urinary proteins, anti-nucleosome, and anti-dsDNA antibodies and negatively correlated with C3 and C4. IL-17A was higher in class III and IV compared to class II and V LN. ROC curve analysis of IL-17A revealed 75% sensitivity and 76.7% specificity for LN, and the AUC was 0.791.
Conclusion
Lupus nephritis patients have a higher serum level of IL-17A than those without LN, which is more pronounced in patients with class-III and IV LN. Moreover, IL-17A has good sensitivity and specificity for LN and correlates with the disease activity indices; hence, it may be a prognostic marker for LN in SLE patients.</description><subject>Arthritis</subject><subject>Autoimmune diseases</subject><subject>Biopsy</subject><subject>Chi-square test</subject><subject>Creatinine</subject><subject>Cytokines</subject><subject>Disease</subject><subject>Hypertension</subject><subject>IL-17A</subject><subject>Laboratories</subject><subject>Lupus</subject><subject>Medicine</subject><subject>Medicine & Public Health</subject><subject>Pathogenesis</subject><subject>Proteins</subject><subject>Rehabilitation</subject><subject>SLE</subject><subject>Ulcers</subject><issn>2090-3235</issn><issn>1110-161X</issn><issn>2090-3235</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2024</creationdate><recordtype>article</recordtype><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9kUFv1DAQhSMEElXpH-BkiXPK2E4cpzdUUVipEhc4W2NnsuttiFPbadVj_3ndBhVOnGY0eu-bGb2q-sjhnHOtPqdGcqVqEE0NIJSu5ZvqREAPtRSyfftP_746S-kIALxVoEGeVI-7OVOcaL3xc807hokhsz78xnhDkY0hsmld1sRmWg7RZ58umAsx0oTZh5nd-3xgg0-EiRi67O98fmB-HryjgpoHdvAphwXzIUxh7x1OzE2Ykh9L_4z4UL0bcUp09qeeVr-uvv68_F5f__i2u_xyXTvJIdcSsHVOWBCDI6W01hylRMJOtg6sdUKqruvIaWwsH60dy5eu7ZSCnkQL8rTabdwh4NEs0ZcXH0xAb14GIe4NxuzdREZYNSqyWomhazQ0vZC8aXsoC3WP41BYnzbWEsPtSimbY1jjXM43Erq26ftiKCqxqVwMKUUaX7dyMM_JmS05U5IzL8kZWUxyM6UinvcU_6L_43oC6c2dCQ</recordid><startdate>20240704</startdate><enddate>20240704</enddate><creator>Ahmed, Aya M.</creator><creator>Ahmed, Abdullatif A.</creator><creator>Ismail, Faten</creator><creator>Elsayed, Sahar A.</creator><general>Springer Berlin Heidelberg</general><general>Springer Nature B.V</general><general>SpringerOpen</general><scope>C6C</scope><scope>AAYXX</scope><scope>CITATION</scope><scope>3V.</scope><scope>7RV</scope><scope>7X7</scope><scope>7XB</scope><scope>8FI</scope><scope>8FJ</scope><scope>8FK</scope><scope>ABUWG</scope><scope>AFKRA</scope><scope>AZQEC</scope><scope>BENPR</scope><scope>CCPQU</scope><scope>DWQXO</scope><scope>FYUFA</scope><scope>GHDGH</scope><scope>K9.</scope><scope>KB0</scope><scope>M0S</scope><scope>NAPCQ</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>DOA</scope><orcidid>https://orcid.org/0009-0007-8414-7040</orcidid><orcidid>https://orcid.org/0000-0001-8755-1750</orcidid><orcidid>https://orcid.org/0000-0002-7315-4524</orcidid><orcidid>https://orcid.org/0009-0003-7688-0358</orcidid></search><sort><creationdate>20240704</creationdate><title>Interleukin-17 as a biomarker for lupus nephritis: correlation with disease activity indices and histopathological classification</title><author>Ahmed, Aya M. ; Ahmed, Abdullatif A. ; Ismail, Faten ; Elsayed, Sahar A.</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c310t-30a5cc2b02dce668881a33aea735c0bbc236777ec8a4b1fbbf001c576609e2503</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2024</creationdate><topic>Arthritis</topic><topic>Autoimmune diseases</topic><topic>Biopsy</topic><topic>Chi-square test</topic><topic>Creatinine</topic><topic>Cytokines</topic><topic>Disease</topic><topic>Hypertension</topic><topic>IL-17A</topic><topic>Laboratories</topic><topic>Lupus</topic><topic>Medicine</topic><topic>Medicine & Public Health</topic><topic>Pathogenesis</topic><topic>Proteins</topic><topic>Rehabilitation</topic><topic>SLE</topic><topic>Ulcers</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Ahmed, Aya M.</creatorcontrib><creatorcontrib>Ahmed, Abdullatif A.</creatorcontrib><creatorcontrib>Ismail, Faten</creatorcontrib><creatorcontrib>Elsayed, Sahar A.</creatorcontrib><collection>SpringerOpen</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Nursing & Allied Health Database</collection><collection>Health & Medical Collection</collection><collection>ProQuest Central (purchase pre-March 2016)</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)</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>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>Nursing & Allied Health Premium</collection><collection>Publicly Available Content Database</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>DOAJ Directory of Open Access Journals</collection><jtitle>Egyptian Rheumatology and Rehabilitation</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Ahmed, Aya M.</au><au>Ahmed, Abdullatif A.</au><au>Ismail, Faten</au><au>Elsayed, Sahar A.</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Interleukin-17 as a biomarker for lupus nephritis: correlation with disease activity indices and histopathological classification</atitle><jtitle>Egyptian Rheumatology and Rehabilitation</jtitle><stitle>Egypt Rheumatol Rehabil</stitle><date>2024-07-04</date><risdate>2024</risdate><volume>51</volume><issue>1</issue><spage>36</spage><epage>7</epage><pages>36-7</pages><artnum>36</artnum><issn>2090-3235</issn><issn>1110-161X</issn><eissn>2090-3235</eissn><abstract>Background
Lupus nephritis (LN) is one of the devastating manifestations of systemic lupus erythematosus (SLE). It is a leading cause of death in SLE patients. Interleukin 17(IL-17) is involved in the development of several autoimmune diseases. It causes inflammation and organ damage by exaggerating the immune response and augmenting antibody production by B cells. We assessed the role of IL-17A in LN and its relation to other markers of disease activity and different histopathological classes.
Results
We evaluated serum IL-17A in forty LN patients and thirty SLE patients without LN (non-LN). We found that LN patients had a significantly higher IL-17A level in comparison to non-LN. In the LN group, IL-17A was positively correlated with the systemic lupus erythematosus disease activity index (SLEDAI), protein/creatinine (P/C) ratio, 24-hour urinary proteins, anti-nucleosome, and anti-dsDNA antibodies and negatively correlated with C3 and C4. IL-17A was higher in class III and IV compared to class II and V LN. ROC curve analysis of IL-17A revealed 75% sensitivity and 76.7% specificity for LN, and the AUC was 0.791.
Conclusion
Lupus nephritis patients have a higher serum level of IL-17A than those without LN, which is more pronounced in patients with class-III and IV LN. Moreover, IL-17A has good sensitivity and specificity for LN and correlates with the disease activity indices; hence, it may be a prognostic marker for LN in SLE patients.</abstract><cop>Berlin/Heidelberg</cop><pub>Springer Berlin Heidelberg</pub><doi>10.1186/s43166-024-00268-3</doi><tpages>7</tpages><orcidid>https://orcid.org/0009-0007-8414-7040</orcidid><orcidid>https://orcid.org/0000-0001-8755-1750</orcidid><orcidid>https://orcid.org/0000-0002-7315-4524</orcidid><orcidid>https://orcid.org/0009-0003-7688-0358</orcidid><oa>free_for_read</oa></addata></record> |
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subjects | Arthritis Autoimmune diseases Biopsy Chi-square test Creatinine Cytokines Disease Hypertension IL-17A Laboratories Lupus Medicine Medicine & Public Health Pathogenesis Proteins Rehabilitation SLE Ulcers |
title | Interleukin-17 as a biomarker for lupus nephritis: correlation with disease activity indices and histopathological classification |
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