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Plasma soluble tumor necrosis factor receptor I as a biomarker of lupus nephritis and disease activity in systemic lupus erythematosus patients
The goal of our study was to evaluate the potential role of sTNF-RI as a biomarker of renal involvement in SLE patients and active SLE. The study sample consisted of two cohorts. The discovery cohort included 16 SLE patients without renal involvement (non-LN), 60 lupus nephritis (LN) patients and 21...
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Published in: | Renal failure 2023-12, Vol.45 (1), p.2174355-2174355 |
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description | The goal of our study was to evaluate the potential role of sTNF-RI as a biomarker of renal involvement in SLE patients and active SLE.
The study sample consisted of two cohorts. The discovery cohort included 16 SLE patients without renal involvement (non-LN), 60 lupus nephritis (LN) patients and 21 healthy controls (HCs) and the replication cohort included 18 SLE non-LN patients, 116 LN patients and 36 HCs.
The sTNF-RI levels differed significantly in the discovery cohort. The plasma sTNF-RI levels were higher in LN patients than in non-LN patients (p = .009) and HCs (p = 4 × 10
−6
). Plasma sTNF-RI levels were significantly higher in non-LN patients than in HCs (p = .03). The finding was confirmed in independent replication cohort (LNs vs. non-LN, p = 4.053 × 10
−7
; LNs vs. HCs, p = 2.395 × 10
−18
; non-LN vs. HCs, p = 2.51 × 10
−4
). The plasma sTNF-RI levels were associated with disease activity, renal function in SLE patients and urine protein in LN patients. The multivariate analysis revealed that high sTNF-RI was an independent risk factor for renal involvement. The multivariate logistic regression results suggested that high TNF-RI, high systolic blood pressure, high serum creatinine, low C4 and positive anti-dsDNA were independent risks of active SLE patients. A nomogram was constructed based on the results of multivariate logistic regression analysis and it was practical in predicting the risk of the active SLE patients. Immunohistochemistry suggested that the expression of TNF-RI in the kidney was increased.
Plasma sTNF-RI might be a good biomarker of renal involvement and disease activity in SLE patients. |
doi_str_mv | 10.1080/0886022X.2023.2174355 |
format | article |
fullrecord | <record><control><sourceid>proquest_pubme</sourceid><recordid>TN_cdi_pubmed_primary_36946374</recordid><sourceformat>XML</sourceformat><sourcesystem>PC</sourcesystem><doaj_id>oai_doaj_org_article_87c7b01984b34c57bdd5b9c93f70726c</doaj_id><sourcerecordid>2871514213</sourcerecordid><originalsourceid>FETCH-LOGICAL-c563t-9263fbebfb39ff991ef82afa88917931c9ff121cc61a91cbdc917445dca0bbc23</originalsourceid><addsrcrecordid>eNp9ks2OFCEUhStG44ytj6AhceOmW36KoljpZOJPJ5PoQhN35ELBNG1VUQI1pp_CV5ayeyaOC1fA5TsHLpyqek7whuAWv8Zt22BKv20opmxDiagZ5w-qc8IpXze4lg-r84VZL9BZ9SSlPcaEt4I-rs5YI-uGifq8-vW5hzQASqGfdW9RnocQ0WhNDMkn5MDkso7W2GmZbBEkBEj7MED8biMKDvXzNKcimXbR56KBsUOdTxaSRUXub3w-ID-idEjZDt6cBDYe8s4OkEMqqwmyt2NOT6tHDvpkn53GVfX1_bsvlx_XV58-bC8vrtaGNyyvJW2Y01Y7zaRzUhLrWgoO2lYSIRkxpUooMaYhIInRnSn1uuadAay1oWxVbY--XYC9mqIv_RxUAK_-FEK8VhCzN71VrTBCYyLbWrPacKG7jmtpJHMCC9qY4vXm6DXNerCdKX1E6O-Z3t8Z_U5dhxtFMGZ8-YlV9erkEMOP2aasBp-M7XsYbZiToqKVghCG64K-_AfdhzmO5a0UbQXhpKaEFYofqeUfU7Tu7jYEqyU_6jY_asmPOuWn6F783cqd6jYwBXh7BPzoQhzgZ4h9pzIc-hBdhNH4pNj_z_gNeMjZZQ</addsrcrecordid><sourcetype>Open Website</sourcetype><iscdi>true</iscdi><recordtype>article</recordtype><pqid>2871514213</pqid></control><display><type>article</type><title>Plasma soluble tumor necrosis factor receptor I as a biomarker of lupus nephritis and disease activity in systemic lupus erythematosus patients</title><source>Taylor & Francis Open Access</source><source>Publicly Available Content Database</source><source>PubMed</source><creator>Liu, Xin-ran ; Qi, Yuan-yuan ; Zhao, Ya-fei ; Cui, Yan ; Zhao, Zhan-zheng</creator><creatorcontrib>Liu, Xin-ran ; Qi, Yuan-yuan ; Zhao, Ya-fei ; Cui, Yan ; Zhao, Zhan-zheng</creatorcontrib><description>The goal of our study was to evaluate the potential role of sTNF-RI as a biomarker of renal involvement in SLE patients and active SLE.
The study sample consisted of two cohorts. The discovery cohort included 16 SLE patients without renal involvement (non-LN), 60 lupus nephritis (LN) patients and 21 healthy controls (HCs) and the replication cohort included 18 SLE non-LN patients, 116 LN patients and 36 HCs.
The sTNF-RI levels differed significantly in the discovery cohort. The plasma sTNF-RI levels were higher in LN patients than in non-LN patients (p = .009) and HCs (p = 4 × 10
−6
). Plasma sTNF-RI levels were significantly higher in non-LN patients than in HCs (p = .03). The finding was confirmed in independent replication cohort (LNs vs. non-LN, p = 4.053 × 10
−7
; LNs vs. HCs, p = 2.395 × 10
−18
; non-LN vs. HCs, p = 2.51 × 10
−4
). The plasma sTNF-RI levels were associated with disease activity, renal function in SLE patients and urine protein in LN patients. The multivariate analysis revealed that high sTNF-RI was an independent risk factor for renal involvement. The multivariate logistic regression results suggested that high TNF-RI, high systolic blood pressure, high serum creatinine, low C4 and positive anti-dsDNA were independent risks of active SLE patients. A nomogram was constructed based on the results of multivariate logistic regression analysis and it was practical in predicting the risk of the active SLE patients. Immunohistochemistry suggested that the expression of TNF-RI in the kidney was increased.
Plasma sTNF-RI might be a good biomarker of renal involvement and disease activity in SLE patients.</description><identifier>ISSN: 0886-022X</identifier><identifier>EISSN: 1525-6049</identifier><identifier>DOI: 10.1080/0886022X.2023.2174355</identifier><identifier>PMID: 36946374</identifier><language>eng</language><publisher>England: Taylor & Francis</publisher><subject>Anti-DNA antibodies ; Biomarkers ; Blood pressure ; Clinical Study ; Creatinine ; disease activity ; Humans ; Immunohistochemistry ; Kidney ; Lupus ; Lupus Erythematosus, Systemic - complications ; Lupus nephritis ; Lupus Nephritis - complications ; Multivariate analysis ; Plasma ; Receptors, Tumor Necrosis Factor ; Regression analysis ; Renal function ; Replication ; Risk factors ; Systemic lupus erythematosus ; Tumor necrosis factor ; tumor necrosis factor receptor ; Tumor necrosis factor-TNF</subject><ispartof>Renal failure, 2023-12, Vol.45 (1), p.2174355-2174355</ispartof><rights>2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2023</rights><rights>2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. This work is licensed under the Creative Commons Attribution License 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><rights>2023 The Author(s). Published by Informa UK Limited, trading as Taylor & Francis Group. 2023 The Author(s)</rights><lds50>peer_reviewed</lds50><oa>free_for_read</oa><woscitedreferencessubscribed>false</woscitedreferencessubscribed><citedby>FETCH-LOGICAL-c563t-9263fbebfb39ff991ef82afa88917931c9ff121cc61a91cbdc917445dca0bbc23</citedby><cites>FETCH-LOGICAL-c563t-9263fbebfb39ff991ef82afa88917931c9ff121cc61a91cbdc917445dca0bbc23</cites></display><links><openurl>$$Topenurl_article</openurl><openurlfulltext>$$Topenurlfull_article</openurlfulltext><thumbnail>$$Tsyndetics_thumb_exl</thumbnail><linktopdf>$$Uhttps://www.ncbi.nlm.nih.gov/pmc/articles/PMC10035946/pdf/$$EPDF$$P50$$Gpubmedcentral$$Hfree_for_read</linktopdf><linktohtml>$$Uhttps://www.proquest.com/docview/2871514213?pq-origsite=primo$$EHTML$$P50$$Gproquest$$Hfree_for_read</linktohtml><link.rule.ids>230,314,723,776,780,881,25731,27479,27901,27902,36989,36990,44566,53766,53768,59116,59117</link.rule.ids><backlink>$$Uhttps://www.ncbi.nlm.nih.gov/pubmed/36946374$$D View this record in MEDLINE/PubMed$$Hfree_for_read</backlink></links><search><creatorcontrib>Liu, Xin-ran</creatorcontrib><creatorcontrib>Qi, Yuan-yuan</creatorcontrib><creatorcontrib>Zhao, Ya-fei</creatorcontrib><creatorcontrib>Cui, Yan</creatorcontrib><creatorcontrib>Zhao, Zhan-zheng</creatorcontrib><title>Plasma soluble tumor necrosis factor receptor I as a biomarker of lupus nephritis and disease activity in systemic lupus erythematosus patients</title><title>Renal failure</title><addtitle>Ren Fail</addtitle><description>The goal of our study was to evaluate the potential role of sTNF-RI as a biomarker of renal involvement in SLE patients and active SLE.
The study sample consisted of two cohorts. The discovery cohort included 16 SLE patients without renal involvement (non-LN), 60 lupus nephritis (LN) patients and 21 healthy controls (HCs) and the replication cohort included 18 SLE non-LN patients, 116 LN patients and 36 HCs.
The sTNF-RI levels differed significantly in the discovery cohort. The plasma sTNF-RI levels were higher in LN patients than in non-LN patients (p = .009) and HCs (p = 4 × 10
−6
). Plasma sTNF-RI levels were significantly higher in non-LN patients than in HCs (p = .03). The finding was confirmed in independent replication cohort (LNs vs. non-LN, p = 4.053 × 10
−7
; LNs vs. HCs, p = 2.395 × 10
−18
; non-LN vs. HCs, p = 2.51 × 10
−4
). The plasma sTNF-RI levels were associated with disease activity, renal function in SLE patients and urine protein in LN patients. The multivariate analysis revealed that high sTNF-RI was an independent risk factor for renal involvement. The multivariate logistic regression results suggested that high TNF-RI, high systolic blood pressure, high serum creatinine, low C4 and positive anti-dsDNA were independent risks of active SLE patients. A nomogram was constructed based on the results of multivariate logistic regression analysis and it was practical in predicting the risk of the active SLE patients. Immunohistochemistry suggested that the expression of TNF-RI in the kidney was increased.
Plasma sTNF-RI might be a good biomarker of renal involvement and disease activity in SLE patients.</description><subject>Anti-DNA antibodies</subject><subject>Biomarkers</subject><subject>Blood pressure</subject><subject>Clinical Study</subject><subject>Creatinine</subject><subject>disease activity</subject><subject>Humans</subject><subject>Immunohistochemistry</subject><subject>Kidney</subject><subject>Lupus</subject><subject>Lupus Erythematosus, Systemic - complications</subject><subject>Lupus nephritis</subject><subject>Lupus Nephritis - complications</subject><subject>Multivariate analysis</subject><subject>Plasma</subject><subject>Receptors, Tumor Necrosis Factor</subject><subject>Regression analysis</subject><subject>Renal function</subject><subject>Replication</subject><subject>Risk factors</subject><subject>Systemic lupus erythematosus</subject><subject>Tumor necrosis factor</subject><subject>tumor necrosis factor receptor</subject><subject>Tumor necrosis factor-TNF</subject><issn>0886-022X</issn><issn>1525-6049</issn><fulltext>true</fulltext><rsrctype>article</rsrctype><creationdate>2023</creationdate><recordtype>article</recordtype><sourceid>0YH</sourceid><sourceid>PIMPY</sourceid><sourceid>DOA</sourceid><recordid>eNp9ks2OFCEUhStG44ytj6AhceOmW36KoljpZOJPJ5PoQhN35ELBNG1VUQI1pp_CV5ayeyaOC1fA5TsHLpyqek7whuAWv8Zt22BKv20opmxDiagZ5w-qc8IpXze4lg-r84VZL9BZ9SSlPcaEt4I-rs5YI-uGifq8-vW5hzQASqGfdW9RnocQ0WhNDMkn5MDkso7W2GmZbBEkBEj7MED8biMKDvXzNKcimXbR56KBsUOdTxaSRUXub3w-ID-idEjZDt6cBDYe8s4OkEMqqwmyt2NOT6tHDvpkn53GVfX1_bsvlx_XV58-bC8vrtaGNyyvJW2Y01Y7zaRzUhLrWgoO2lYSIRkxpUooMaYhIInRnSn1uuadAay1oWxVbY--XYC9mqIv_RxUAK_-FEK8VhCzN71VrTBCYyLbWrPacKG7jmtpJHMCC9qY4vXm6DXNerCdKX1E6O-Z3t8Z_U5dhxtFMGZ8-YlV9erkEMOP2aasBp-M7XsYbZiToqKVghCG64K-_AfdhzmO5a0UbQXhpKaEFYofqeUfU7Tu7jYEqyU_6jY_asmPOuWn6F783cqd6jYwBXh7BPzoQhzgZ4h9pzIc-hBdhNH4pNj_z_gNeMjZZQ</recordid><startdate>202312</startdate><enddate>202312</enddate><creator>Liu, Xin-ran</creator><creator>Qi, Yuan-yuan</creator><creator>Zhao, Ya-fei</creator><creator>Cui, Yan</creator><creator>Zhao, Zhan-zheng</creator><general>Taylor & Francis</general><general>Taylor & Francis Ltd</general><general>Taylor & Francis Group</general><scope>0YH</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>3V.</scope><scope>7T5</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>H94</scope><scope>M2O</scope><scope>MBDVC</scope><scope>PIMPY</scope><scope>PQEST</scope><scope>PQQKQ</scope><scope>PQUKI</scope><scope>PRINS</scope><scope>Q9U</scope><scope>7X8</scope><scope>5PM</scope><scope>DOA</scope></search><sort><creationdate>202312</creationdate><title>Plasma soluble tumor necrosis factor receptor I as a biomarker of lupus nephritis and disease activity in systemic lupus erythematosus patients</title><author>Liu, Xin-ran ; Qi, Yuan-yuan ; Zhao, Ya-fei ; Cui, Yan ; Zhao, Zhan-zheng</author></sort><facets><frbrtype>5</frbrtype><frbrgroupid>cdi_FETCH-LOGICAL-c563t-9263fbebfb39ff991ef82afa88917931c9ff121cc61a91cbdc917445dca0bbc23</frbrgroupid><rsrctype>articles</rsrctype><prefilter>articles</prefilter><language>eng</language><creationdate>2023</creationdate><topic>Anti-DNA antibodies</topic><topic>Biomarkers</topic><topic>Blood pressure</topic><topic>Clinical Study</topic><topic>Creatinine</topic><topic>disease activity</topic><topic>Humans</topic><topic>Immunohistochemistry</topic><topic>Kidney</topic><topic>Lupus</topic><topic>Lupus Erythematosus, Systemic - complications</topic><topic>Lupus nephritis</topic><topic>Lupus Nephritis - complications</topic><topic>Multivariate analysis</topic><topic>Plasma</topic><topic>Receptors, Tumor Necrosis Factor</topic><topic>Regression analysis</topic><topic>Renal function</topic><topic>Replication</topic><topic>Risk factors</topic><topic>Systemic lupus erythematosus</topic><topic>Tumor necrosis factor</topic><topic>tumor necrosis factor receptor</topic><topic>Tumor necrosis factor-TNF</topic><toplevel>peer_reviewed</toplevel><toplevel>online_resources</toplevel><creatorcontrib>Liu, Xin-ran</creatorcontrib><creatorcontrib>Qi, Yuan-yuan</creatorcontrib><creatorcontrib>Zhao, Ya-fei</creatorcontrib><creatorcontrib>Cui, Yan</creatorcontrib><creatorcontrib>Zhao, Zhan-zheng</creatorcontrib><collection>Taylor & Francis Open Access</collection><collection>Medline</collection><collection>MEDLINE</collection><collection>MEDLINE (Ovid)</collection><collection>MEDLINE</collection><collection>MEDLINE</collection><collection>PubMed</collection><collection>CrossRef</collection><collection>ProQuest Central (Corporate)</collection><collection>Immunology Abstracts</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>AIDS and Cancer Research Abstracts</collection><collection>ProQuest research library</collection><collection>Research Library (Corporate)</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>ProQuest Central Basic</collection><collection>MEDLINE - Academic</collection><collection>PubMed Central (Full Participant titles)</collection><collection>DOAJ Directory of Open Access Journals</collection><jtitle>Renal failure</jtitle></facets><delivery><delcategory>Remote Search Resource</delcategory><fulltext>fulltext</fulltext></delivery><addata><au>Liu, Xin-ran</au><au>Qi, Yuan-yuan</au><au>Zhao, Ya-fei</au><au>Cui, Yan</au><au>Zhao, Zhan-zheng</au><format>journal</format><genre>article</genre><ristype>JOUR</ristype><atitle>Plasma soluble tumor necrosis factor receptor I as a biomarker of lupus nephritis and disease activity in systemic lupus erythematosus patients</atitle><jtitle>Renal failure</jtitle><addtitle>Ren Fail</addtitle><date>2023-12</date><risdate>2023</risdate><volume>45</volume><issue>1</issue><spage>2174355</spage><epage>2174355</epage><pages>2174355-2174355</pages><issn>0886-022X</issn><eissn>1525-6049</eissn><abstract>The goal of our study was to evaluate the potential role of sTNF-RI as a biomarker of renal involvement in SLE patients and active SLE.
The study sample consisted of two cohorts. The discovery cohort included 16 SLE patients without renal involvement (non-LN), 60 lupus nephritis (LN) patients and 21 healthy controls (HCs) and the replication cohort included 18 SLE non-LN patients, 116 LN patients and 36 HCs.
The sTNF-RI levels differed significantly in the discovery cohort. The plasma sTNF-RI levels were higher in LN patients than in non-LN patients (p = .009) and HCs (p = 4 × 10
−6
). Plasma sTNF-RI levels were significantly higher in non-LN patients than in HCs (p = .03). The finding was confirmed in independent replication cohort (LNs vs. non-LN, p = 4.053 × 10
−7
; LNs vs. HCs, p = 2.395 × 10
−18
; non-LN vs. HCs, p = 2.51 × 10
−4
). The plasma sTNF-RI levels were associated with disease activity, renal function in SLE patients and urine protein in LN patients. The multivariate analysis revealed that high sTNF-RI was an independent risk factor for renal involvement. The multivariate logistic regression results suggested that high TNF-RI, high systolic blood pressure, high serum creatinine, low C4 and positive anti-dsDNA were independent risks of active SLE patients. A nomogram was constructed based on the results of multivariate logistic regression analysis and it was practical in predicting the risk of the active SLE patients. Immunohistochemistry suggested that the expression of TNF-RI in the kidney was increased.
Plasma sTNF-RI might be a good biomarker of renal involvement and disease activity in SLE patients.</abstract><cop>England</cop><pub>Taylor & Francis</pub><pmid>36946374</pmid><doi>10.1080/0886022X.2023.2174355</doi><tpages>1</tpages><oa>free_for_read</oa></addata></record> |
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source | Taylor & Francis Open Access; Publicly Available Content Database; PubMed |
subjects | Anti-DNA antibodies Biomarkers Blood pressure Clinical Study Creatinine disease activity Humans Immunohistochemistry Kidney Lupus Lupus Erythematosus, Systemic - complications Lupus nephritis Lupus Nephritis - complications Multivariate analysis Plasma Receptors, Tumor Necrosis Factor Regression analysis Renal function Replication Risk factors Systemic lupus erythematosus Tumor necrosis factor tumor necrosis factor receptor Tumor necrosis factor-TNF |
title | Plasma soluble tumor necrosis factor receptor I as a biomarker of lupus nephritis and disease activity in systemic lupus erythematosus patients |
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